SPARC is a matricellular protein that is involved in both pancreatic cancer and diabetes. It belongs to a wider family of proteins that share structural and functional similarities. Relatively little is known about this extended family, but evidence of regulatory interactions suggests the importance of a holistic approach to their study. We show that Hevin, SPOCKs, and SMOCs are strongly expressed within islets, ducts, and blood vessels, suggesting important roles for these proteins in the normal pancreas, while FSTL-1 expression is localised to the stromal compartment reminiscent of SPARC. In direct contrast to SPARC, however, FSTL-1 expression is reduced in pancreatic cancer. Consistent with this, FSTL-1 inhibited pancreatic cancer cell proliferation. The complexity of SPARC family proteins is further revealed by the detection of multiple cell-type specific isoforms that arise due to a combination of post-translational modification and alternative splicing. Identification of splice variants lacking a signal peptide suggests the existence of novel intracellular isoforms. This study underlines the importance of addressing the complexity of the SPARC family and provides a new framework to explain their controversial and contradictory effects. We also demonstrate for the first time that FSTL-1 suppresses pancreatic cancer cell growth.
The extracellular matrix (ECM) provides both structural support and regulates cellular responses. Diabetes results from an insufficiency of insulin-producing islet β cells and a failure of compensatory β cell growth and regeneration1. Worldwide, diabetes affects 415 million people and this figure is estimated to increase to 642 million by 20402. The discovery of therapeutic mechanisms to stimulate β cell growth would allow physiological control of glucose levels and avoid many of the side effects and risks associated with poorly managed disease1. The pancreas is also the site of one of the most lethal types of cancer. Pancreatic ductal adenocarcinoma (PDAC) arises in the ductal epithelial cells of the pancreas and has one of the lowest 5-year survival rates of all cancers (<5%). It also ranks as the seventh most common cause of death from cancer worldwide3. An underlying feature common to both diseases is the dysregulation of cell growth and survival, in which the extracellular matrix is likely to play an important regulatory role.
Pancreatic islets are surrounded by a basement membrane composed of ECM proteins such as collagens, laminin, and fibronectin4,5,6. Islets cultured in a collagen matrix showed improved β cell mass, survival and glucose stimulated-insulin secretion compared to islets cultured in 2D7,8. The ECM and associated integrin signalling have also been implicated in the pathogenesis of diabetes. For example, mice deficient in β1 integrin have decreased β cell mass, proliferation, glucose tolerance and insulin production9,10.
In pancreatic cancer, the production of collagens I, III, and fibronectin is increased11,12,13 and matrix remodelling enzymes such as MMPs and their inhibitors contribute to pancreatic cancer progression and metastasis14,15. Disruption of the basement membrane composition can lead to changes in apicobasal polarity and cause changes in cell shape and behavior. This has been shown to drive increased cell proliferation and tumourigenesis16,17,18. Stromal cells such as stellate cells, fibroblasts, endothelial cells and macrophages produce ECM proteins and also growth factors and cytokines that make up the extracellular environment. One of the hallmarks of PDAC is an extensive stroma that creates a protective capsule around the tumour and can constitute up to 80% of the tumour mass19. Indeed, the tumour-stroma itself is now considered a therapeutic target in pancreatic cancer20,21. The regulation of cell growth and migration by the ECM and stromal cells underlies their important role in the progression of both pancreatic cancer and diabetes.
Central to the regulation of ECM structure and cell-matrix interactions are non-structural matricellular proteins such as the SPARC family22. SPARC, or secreted protein acidic and rich in cysteine, is produced by stromal cells and regulates matrix remodelling and cell-matrix interactions23. SPARC has been shown to regulate cell adhesion and there is also evidence for a role in the regulation of cell growth and proliferation. SPARC modulates cell growth responses to a range of growth factors including TGF-β24,25,26,27,28,29,30, binds to both β1 integrins and collagen, and regulates collagen assembly and fibrillogenesis31,32,33. Hence SPARC determines cell responses to the ECM and controls multiple pathways fundamental to cell growth and adhesion.
SPARC is known to be highly expressed during development, wound healing and tissue regeneration and to play a role in angiogenesis, tumourigenesis and fibrosis23,34,35. In pancreatic cancer, stromal SPARC over-expression is strongly associated with poor patient prognosis36,37. Insulin resistance, diabetes and obesity are also associated with elevated levels of SPARC38,39,40. We have previously shown that SPARC is expressed by pancreatic stromal cells and is localised to the islet basement membrane. SPARC inhibits β cell and islet responses to growth factors28 and can also influence β cell function41. The production of SPARC by pancreatic stellate cells is regulated by metabolic parameters suggesting that SPARC may influence β cell loss and dysfunction in patients with type 2 diabetes28. SPARC is therefore involved in a number of pancreatic diseases, and SPARC expression and function in the pancreas is relatively well characterised. However, very little is known about the wider SPARC family of proteins, despite structural and functional similarities that suggest potentially similar roles.
The wider SPARC family consists of seven additional proteins: SPARC-like 1 or Hevin, SPOCK-1, -2, & -3, SMOC-1 and -2, and FSTL-1. As shown in Fig. 1, these proteins share three main domains: domain I – a highly acidic region with low affinity calcium binding; domain II- a follistatin-like domain consisting of kazal-like domains involved in growth factor binding; and domain III- a high affinity calcium binding domain with 2 EF hands [also known as the EC domain] that is involved in collagen interactions. The EC and follistatin-like domains are well conserved within the family. In contrast, domain I is highly variable and, other than retaining an overall acidic nature, can be regarded as distinct in each SPARC family protein. In addition to these three domains, thyroglobulin domains are present in the SPOCK and SMOC proteins, a glycosaminoglycan-binding domain is present in the SPOCK proteins, and FSTL-1 contains a von Willebrand factor type-C domain.
Hevin is structurally the closest relative of SPARC and the two proteins have many overlapping roles. Like SPARC, Hevin can be anti-adhesive, modulates cell shape, binds to collagen and regulates collagen assembly42,43,44,45. While the role of Hevin in diabetes has not yet been examined, Hevin has been implicated in many cancers. Similar to SPARC, Hevin mRNA is overexpressed in pancreatic cancer compared to normal tissue. In fact, it has been suggested that proteolytic cleavage of Hevin creates a ‘SPARC-like fragment’ that can functionally compensate for SPARC, and that as such Hevin acts as a SPARC reservoir46,47.
The SPOCK proteins also influence matrix characteristics, primarily through MMP regulation. For example, SPOCK-1 and SPOCK-3 inhibit membrane-type MMP (MT-MMP) activation of pro-MMP248, while SPOCK-2 abrogates the inhibition of MT-MMPs by SPOCK-1 and SPOCK-349. MMPs are important regulators of cell migration and cell proliferation, for example through TGF-β activation50. The role of SPOCKs in diabetes is unknown but, as for SPARC, high expression of SPOCK-1 in the desmoplastic stroma of PDAC has been associated with poor prognosis51. In other cancers, the increase in SPOCK-1 expression by TGF-β is thought to be involved in epithelial-mesenchymal transition (EMT)52, and tumour invasion of glioma cells was inhibited by SPOCK-3 transfection49. These studies suggest a role for SPOCK proteins in matrix remodelling and metastasis, and emphasize the importance of co-regulation between the SPOCK subfamily of proteins.
Although the role of SMOC proteins in the pancreas has not yet been examined, SMOC-1 is known to be an antagonist for TGF-β superfamily-BMP proteins53 and is important for stem cell differentiation54. SMOC-1 may also influence tissue remodelling by interaction with the matricellular protein tenascin-C55. In breast cancer, the SMOC-1 gene was found to be hypermethylated56 but otherwise very little is known about the role of SMOC-1 in human disease. There is similarly little known about the role of SMOC-2, although there is evidence that SMOC-2 has mitogenic properties and is an important regulator of proliferation57, and can synergise with VEGF and bFGF-induced angiogenesis in endothelial cells58. Like SPARC, SMOC-2 may therefore regulate growth factor signalling. As for many matricellular proteins, SMOC-2 can also bind to integrins, and can promote cell attachment and focal adhesion formation59.
FSTL-1 has the lowest homology to SPARC. It was first discovered as a TGF-β-induced protein and it has also been shown to bind directly to the TGF-β superfamily including BMPs60,61. In bone cancer cells, FSTL-1 was shown to promote metastasis62. On the other hand, the opposite was observed in ovarian and endometrial cancers where FSTL-1 was reported to be a tumour suppressor and increased the expression of apoptotic molecules such as caspases, and inhibited MMP2 expression and cell invasion63. As yet, the role of FSTL-1 in pancreatic cancer and diabetes is unknown. However, FSTL-1 is closely related to other follistatin-like proteins that have been implicated in pancreatic diseases. For example, FSTL-2, also known as IGFBP-7, is associated with insulin resistance and type II diabetes64,65, and FSTL-2 down-regulation is associated with poor prognosis in PDAC patients66. Furthermore, FSTL-3 knockout mice have increased pancreatic islet number and improved insulin sensitivity67.
Hence, there is evidence that the extended SPARC family of proteins play similar roles to SPARC in regulating both the matrix and cellular responses to their environment. There is also growing evidence of coordinated regulation between SPARC family members, for example interactions between SPOCK proteins that regulate their function, and the potential overlapping function of Hevin and SPARC68. The presence of active proteolytic fragments further adds to this complexity, and the SPARC family of proteins can also interact with other matricellular proteins. For example, SPARC interacts with TSP-169, and SMOC-1 with tenascin-C55. Ultimately, it will therefore be necessary to dissect the complexity and interactions of the SPARC family of matricellular proteins, and this may help resolve some of the contradictions and controversy regarding their function. The urgency is enhanced by the clinical importance of SPARC and other matricellular proteins as potential biomarkers and therapeutic targets70. To achieve this it will be necessary to take a systematic approach to understanding the function and complexity of the SPARC family of proteins. The aim of this study was therefore to investigate the expression of the extended SPARC family in the pancreas and provide a holistic analysis addressing their complexity in order to understand their role in pancreatic diseases.
Results and Discussion
Expression of the SPARC family of proteins in the pancreas
We have previously defined the expression of SPARC in the pancreas28, but the expression of other members of the SPARC family is currently not known. We therefore used immunohistochemistry to analyse the expression of all members of the wider SPARC family of proteins in pancreas sections, examining expression specifically in islets, ducts and blood vessels.
Hevin was detected throughout the islets, with stronger staining in selected cells primarily at the islet periphery, as shown by the solid arrows in Fig. 2a panels (i) & (ii). In these cells, Hevin staining was observed primarily in the cytoplasm, although nuclear staining is apparent in some islet cells. Staining of the islet basement membrane was also observed, as indicated by the dotted arrows in (i). Hevin was also expressed in blood vessels (iii), in connective tissues (iv), in ductal cells (v), and in selected cells in the acinar tissue (vi). Hevin expression in the normal mouse pancreas is therefore distinct to that observed in the human pancreas, where expression is much more restricted, and in islets appears localised specifically to stromal cells71, as we have observed previously for SPARC28.
As shown in Figs 2 and 3, the SPOCKs are also detected throughout islets, with strikingly strong expression of SPOCK-1 and SPOCK-3 in particular. The SPOCKs are also expressed in blood vessels, ductal cells and ductal basement membranes, and in selected acinar cells. SPOCK-1 staining was observed in the cytoplasm (Fig. 2b i–iii) but could also clearly be observed at the cell surface or extracellularly in ducts and in selected islet cells (arrows in Fig. 2b i and v), and was largely absent in the nucleus. A distinct perinuclear staining was observed in selected acinar cells (arrow in Fig. 2b vi). Similar to Hevin, SPOCK-2 also showed higher expression in cells at the islet periphery, and again staining was primarily evident in the cytoplasm as shown in Fig. 2c(i & ii). SPOCK-3 was highly expressed in all islet cells and with primarily a cytoplasmic staining pattern (Fig. 3a i–iii), although a more restricted perinuclear staining was observed in scattered cells throughout the acinar tissue (Fig. 3a vi). The high levels of SPOCK expression in islets suggests that these proteins may play an important role in normal islet function, and it will be important for future studies to examine this further.
Both SMOC-1 (Fig. 3b) and SMOC-2 (Fig. 3c) were detected throughout the islet, with a range of staining intensity in different cells. For both proteins, the staining was again largely cytoplasmic, though strong nuclear SMOC-1 staining could also be observed in selected cells (eg arrow in Fig. 3b iii). The SMOCs were also expressed in blood vessels, in ductal cells (Fig. 3b and c panels iv, v & solid arrows in vi), as well as in the surrounding connective tissue (dotted arrows in vi).
Within islets, FSTL-1 was expressed primarily in blood vessels and the islet basement membrane, although some weak diffuse staining can be observed throughout the islet (Fig. 4 i & ii). FSTL-1 was also expressed in large and small blood vessels throughout the endocrine and exocrine pancreas as well as in connective tissue (iii & iv). In ducts, FSTL-1 was clearly detected at the cell surface (vi), although some staining was also observed in the cytoplasm of ductal cells (v).
The SPARC family are defined as secreted matricellular proteins and contain signal peptide sequences to target them to the secretory pathway, as indicated in Fig. 1 (confirmed by Phobius database). They were therefore expected to be observed extracellularly. While Hevin, SPOCK-1 and FSTL-1 staining was observed at the cell surface, all members of the SPARC family also demonstrated cytoplasmic staining, and in some cases staining in the nucleus could also be observed. Cytoplasmic staining of SPARC family proteins has been previously described for Hevin72, SPOCK-173 and SMOC-259,74. It is likely that all SPARC family proteins are present in the extracellular environment, but this is not easily observed by immunohistochemistry when there is extensive cytoplasmic staining. However, the staining we observe clearly demonstrates the presence intracellularly of all SPARC family proteins. It will therefore be important to consider a possible intracellular role for these proteins in addition to their function in the extracellular matrix. One potential explanation for the intracellular location of these proteins is expression of splice variants lacking the signal peptide, and this is explored further below.
In summary, Hevin, the SPOCKs and the SMOCs were strongly expressed throughout islets consistent with expression in β cells. Furthermore, Hevin, SPOCK-2, and SMOC-2 showed stronger staining in cells at the islet periphery, consistent with higher expression in α cells. All SPARC family proteins were detected in ductal cells, while SPOCK-1, -2, -3, SMOC-1, and FSTL-1 were found also in ductal basement membranes. Hevin, the SPOCKs, the SMOCs and FSTL-1 were all found in selected acinar cells and in blood vessels throughout the pancreas. FSTL-1 on the other hand was not strongly expressed in islet parenchymal cells, but instead staining was consistent with expression primarily in islet basement membranes and blood vessels. This suggests that FSTL-1 is likely to be primarily expressed by stromal cells such as fibroblasts and endothelial cells, and the FSTL-1 staining pattern is highly reminiscent of SPARC expression28. The SPARC family of proteins are therefore clearly expressed in the pancreas, specifically in islet cells, stromal cells and pancreatic ducts, and warrant further investigation as to their function within the pancreas.
Identification of multiple isoforms of the SPARC family and their expression in specific pancreatic cell types
In order to confirm the expression of SPARC family proteins observed in pancreas sections, we analysed expression in specific cell types by western blot. Protein quantification was performed to ensure equal loading. Given that cell lysates were obtained from different cell types with variable actin expression it was not possible to standardise the samples to compensate for small variations in loading, and therefore only a qualitative analysis was performed.
Hevin was expressed in both INS-1 and MIN-6 β cells (Fig. 5a), in agreement with the islet staining pattern observed using immunohistochemistry, and was also expressed by stromal cells such as PS-1 stellate cells, MRC5 fibroblasts and HUVEC endothelial cells, consistent with staining in basement membranes and blood vessels. SPOCK-1, -2, and -3 were also clearly detectable in both β cell lines examined (Fig. 5b–d), consistent with staining in islet cells shown by immunohistochemistry, and were also expressed in stromal cells such as stellate cells, fibroblasts and endothelial cells. Although only weakly detected in MIN-6 cells, SMOC-1 was strongly expressed in INS-1 β cells (Fig. 5e), consistent with the IHC staining. SMOC-1 was also detected in endothelial cells, but is either absent or very weakly expressed in fibroblast and stellate cells. SMOC-2 on the other hand was not detected by western blotting (data not shown). FSTL-1 was not detected in β cells, consistent with the absence of staining in the majority of islet cells by immunohistochemistry. Instead, FSTL-1 was primarily detected in PS-1 stellate cells, with weak expression in fibroblasts and endothelial cells (Fig. 5f) consistent with basement membrane and blood vessel-like staining in pancreas sections.
A further striking observation in the series of western blotting experiments in Fig. 5 is the presence of multiple bands for all SPARC family proteins, with the exception of FSTL-1. We also observed clear evidence of cell-type specific expression of these isoforms. For example, amongst the cell types examined endothelial cells uniquely express a 65 kDa variant of SMOC-1. Similarly, only pancreas-derived cells expressed a 110 kDa isoform of Hevin, while β cells uniquely express high levels of an additional 39 kDa isoform. A summary of molecular weights detected for each protein is shown in Suppl. Table 1. As far as we are aware this is the first systematic analysis of multiple isoforms of the extended SPARC family of proteins. The identity of these isoforms and the mechanisms underlying the cell-type specific expression are not known. However, cell type specific expression of isoforms may well in part explain some of the contradictory and controversial effects of the SPARC family of proteins on cell function, and their often complex association with clinical diseases75.
Possible explanations for the observation of multiple isoforms include: (1) post-translational modifications such as phosphorylation, glycosylation and addition of glycosaminoglycans, (2) protein cleavage into peptide fragments46,47, (3) expression of alternative splice variants, (4) the use of alternative translational start sites76 and (5) cross-linking by transglutaminase77,78. We therefore performed a systematic analysis of these factors for the wider SPARC family of proteins, combining both bioinformatics and experimental approaches.
Post-translational modification of the wider SPARC family of proteins
Potential glycosylation and phosphorylation sites for each extended family of SPARC protein were identified using GeneCards, UniProt, and Phosphosite Plus. As shown in Suppl. Table 2, Hevin can be extensively modified, with 12 potential glycosylation sites and 8 phosphorylation sites. The SPOCKs also contain sites for both glycosylation and phosphorylation, and are known to contain O-linked glycosaminoglycans at serine residues in the C’ terminal region (Suppl. Table 2 and Figure 1). Glycosaminoglycan linkage can increase the molecular weight by 20 kDa or more79. SMOC-1 can be extensively modified through 9 glycosylation sites, compared to SMOC-2 with only 2 sites. Lastly, FSTL-1 has up to 3 sites for glycosylation and up to 5 for phosphorylation. All proteins in the extended SPARC family can therefore undergo varying degrees of post-translational modification.
Alternative splicing of the SPARC family of proteins
We previously performed an initial analysis of alternative splice variation in matricellular proteins80. To determine whether the protein isoforms observed in Fig. 5 could be due to alternative splicing we further analysed the SPARC family splice variants banked in the ENSEMBL database. As shown in Suppl. Table 3, there is evidence of a large number of splice variants for the SPARC family of proteins. In particular, 17 coding variants were identified for SPOCK-3. However, since some coding sequences (CDS) were found to be incomplete, we restricted our further analysis to coding variants for which the complete CDS is known. Protein FASTA sequences were obtained for complete CDS transcripts and domain structures were predicted using the InterPro database. As shown in Fig. 6, in many cases multiple splice variants encode highly similar proteins. However, for each of the extended SPARC family of proteins at least one alternative splice variant with distinct protein sequence was identified. In particular, for Hevin, SPOCK-1, SPOCK-3 and SMOC-2 at least one alternative variant lacking the signal peptide was identified, suggesting that both intracellular and extracellular isoforms of these proteins exist. The intracellular isoforms may explain the cytoplasmic staining for these proteins described in Fig. 1. It is also possible that intracellular isoforms exist for SPOCK-2, SMOC-1 and FSTL-1 for which the complete sequence is not yet known and was therefore not included in this analysis.
Perhaps the most striking difference between isoforms of the extended SPARC family is the size of the acidic domain I, suggesting functional significance of domain I variation. However, the role of this domain is not well understood. Domain I is known to bind to calcium but with low affinity compared to the EC domain, and in SPARC domain I is involved in the regulation of cell migration81. In SPOCK-3, the acidic domain I is involved in MT-MMP inhibition48 while in SPOCK-2 it is involved in its regulation of SPOCK-349. This domain has diverged and acquired additional acidic residues during evolution82,83,84,85. It is also the least conserved domain between different SPARC family proteins, and is the primary feature that distinguishes SPARC from Hevin. Domain I may therefore confer diversity of function to each SPARC family protein, and this diversity is then further expanded by alternative splicing. This analysis therefore suggest the functional importance of domain I variation in the SPARC family of proteins.
Hevin isoforms – analysis of post-translational modification and splice variants
As described above, cell-specific expression of 110 kDa and 39 kDa Hevin isoforms was observed in addition to a widely expressed 49 kDa isoform. The predicted molecular weight of the Hevin precursor protein encoded by the primary transcript is 75 kDa, and the known Hevin splice variants for which the complete CDS is known are unlikely to explain the isoforms observed (Suppl. Table 3). However, 39–49 kDa Hevin bands have been reported to arise from cleavage by ADAMTS4 and MMP3, and Hevin is also a substrate for thrombin and plasmin digestion46,47. These low molecular weight Hevin proteins (39 and 49 kDa) are therefore likely to represent the products of enzymatic cleavage. The presence of the 39 kDa fragment exclusively in β cells suggests additional proteolytic cleavage of Hevin in these cells, perhaps reflecting a β cell specific role for Hevin fragments.
High molecular weight Hevin-reactive bands have also been previously observed44,45,46,86. Based on the number of predicted glycosylation sites (Suppl. Table 2), we hypothesized that the 110 kDa band is likely to reflect extensive glycosylation. To test this, we digested PS-1 stellate cell lysates with PNGase-F to test for the presence of N-linked glycosylation. As shown in Fig. 7a, an additional band at 36 kDa appeared following de-glycosylation. However, only the 49 kDa band and not the 110 kDa band showed any detectable decrease in intensity. The Hevin antibody used in these experiments recognises an epitope in the N-terminus and would therefore be predicted to recognise N-terminal cleavage products. These results therefore suggest that the 49 kDa band is a 36 kDa N-terminal cleavage product with approximately 15 kDa of N-linked glycosylation. The full length 110 kDa isoform may be conformationally resistant to glycosylase treatment or consist primarily of O-linked glycosylation. Alternatively, Hevin is predicted to be a substrate of transglutaminase (TRANSDAB)87, and the 110 kDa band may therefore represent oligomer formation due to cell-type specific cross-linking. Supporting this hypothesis, SPARC is also known to form oligomers as a result of transglutaminase-mediated cross-linking77,88.
Although no direct evidence of Hevin splice variants was observed in these experiments, subsequent experiments using an alternative Hevin antibody recognising a C’ epitope revealed the presence of an additional third isoform in PS-1 cells at approximately 60 kDa (Suppl. Figure 1), whereas only two isoforms were detected in PS-1 cells with the N’ antibody. This observation could suggest the presence of an alternative splice variant lacking the N-terminus. Consistent with this, Hevin variant 005 has a predicted molecular weight of 62 kDa (Suppl. Table 3). Since this variant lacks a portion of the N-terminal region it may exist in a conformation that is not recognised by the N-terminal antibody used. Variant 005 lacks a signal peptide and is predicted to be an intracellular isoform. However, mRNA studies would be required to confirm the detection of this potentially novel intracellular Hevin splice variant.
Proteolytic cleavage of Hevin has been shown to produce a “SPARC-like fragment”46,47 that is likely to correspond to, or be contained within, the approximately 50 kDa band detected using the C-terminal Hevin antibody (Suppl. Figure 1). It has been suggested that this SPARC-like fragment may compensate for the loss of SPARC expression44,46,89. SPARC can be suppressed for example as a result of SPARC promoter methylation during tumourigenesis90. Furthermore, SPARC and Hevin have overlapping and compensatory roles in angiogenesis inhibition91. We therefore tested whether reducing SPARC expression in PS-1 stellate cells by siRNA knockdown results in a compensatory increase in the presence of proteolytic cleavage products detected by both the N’- and C’-antibodies. As shown in Fig. 7b–e, despite achieving 90% knockdown of SPARC expression, no significant change in the detection of either the full length Hevin or smaller fragments was observed with either the N-terminal or C-terminal antibodies.
Therefore, although previous reports have suggested that C-terminal Hevin fragments may compensate for loss of SPARC expression, we did not find evidence to support this hypothesis within the cell types examined. However, the various isoforms of Hevin that we have observed are likely to have distinct properties and to fulfill specific functions within the particular cell types where they are expressed, and there is evidence for the importance of additional proteolytic cleavage products specifically in β cells.
SPOCK protein isoforms
For each of the SPOCK proteins three different isoforms were observed. In the case of SPOCK-1, while an isoform of the predicted molecular weight (49 kDa) was observed in all cell lines examined, two additional isoforms (56 kDa and 100 kDa) were observed specifically in pancreatic stellate cells and β cells (Fig. 5b). SPOCK-1 has previously been detected in the 130–150 kDa range in human plasma and in kidney cells, and the increase in molecular weight is most likely due to the addition of large glycosaminoglycan chains (both chondroitin and heparin sulphate chains) at residues 383 and 388 of the C-terminus (Suppl. Table 2)79,92. The detection of SPOCK-1 at 49 kDa in all cell types suggests a native unglycosylated form of SPOCK-1 is also widely produced, and the addition of glycosaminoglycans in specific cell types may create novel functions. A 33 kDa intracellular alternative splice variant was also identified in ENSEMBL (Suppl. Table 3 and Figure 6), and it is also possible that the observed 49 kDa and 56 kDa isoforms represent glycosylated forms of this variant.
Multiple splice variants of SPOCK-2 were also identified in ENSEMBL, primarily encoding variants highly similar to the primary transcript, with the exception of variant 202 that encodes a small (8 kDa) protein containing a signal peptide but lacking any conserved domains (Fig. 6). However, proteins of such low molecular weight would not be observed by our western blot analysis. Proteins of around the expected molecular weight of the primary and similar transcripts (47 kDa) were observed in fibroblast and endothelial cells, though not in pancreatic stellate and β cells (Suppl. Table 1 and Figure 5c). In contrast, in β cells SPOCK-2 was detected at 60 kDa and 120 kDa. As shown in Suppl. Table 2, SPOCK-2 contains both glycan and glycosaminoglycan binding sites, and variable glycosylation is therefore likely to explain the larger isoforms observed specifically in β cells. Interestingly, pancreatic stellate cells express very low levels of SPOCK-2.
For SPOCK-3 a large number of alternative transcripts were identified in ENSEMBL, with a total of 13 protein-coding variants for which the complete coding sequence is known (Suppl. Table 3). Of these, multiple transcripts are predicted to produce a 49 kDa protein that is highly similar to the primary transcript in terms of predicted domain structure (001, 002, 006, 012, 014, 015, 016), as shown in Fig. 6. Interestingly, variants lacking certain domains or with additional domains were also identified, encoding proteins of varying molecular weights between 36 and 44 kDa. For example, transcript 005 lacks the thyroglobulin domain and C’ glycosaminoglycan binding domain, while transcript 010 lacks the follistatin domain (Fig. 6). An alternative splice variant of SPOCK-3 missing the thyroglobulin domain and glycosaminoglycan binding sites has been previously described in kidney cells and glioma, referred to as N-Tes, that is likely to correspond to variant 005 in ENSEMBL48. SPOCK-3 transcript 013 contains a second thyroglobulin domain situated before the EC domain, almost pseudo-SMOC-like in structure. Interestingly, the thyroglobulin domain is involved in the IGF binding properties of IGFBPs, as well as protease inhibitory functions93,94,95,96, and it will therefore be interesting to test the function of splice variants either lacking (005) or with additional (013) thyroglobulin domains. SPOCK-3 splice variants also contain extensive variation within the acidic N-terminus, and this domain varies from just 12 amino acids in transcript 202, compared to 129 amino acids in the primary transcript. Importantly, transcripts 201, 017 and 202 all lack the signal peptide and therefore are predicted to be intracellular proteins, consistent with the intracellular staining we observed in Fig. 3.
Since SPOCK-3 can also be glycosylated (Suppl. Table 2), the 65 kDa stromal isoform is likely to correspond to a glycosylated form of the 49 kDa protein encoded by the primary or similar transcripts. In order to test whether the variants we observe are due to glycosylation, we subjected PS-1 cell lysates to PNGase-F digestion. As shown in Fig. 8a, the 34 kDa isoform increases in intensity by at least four fold following digestion, suggesting that this isoform is present in both N-linked glycosylated and unglycosylated forms, and that the 34 kDa isoform is the unglycosylated form. Furthermore, a second band of 45 kDa also appears following digestion, suggesting the presence of a second distinct protein isoform that is normally N-glycosylated. The size of this band is consistent with the primary transcript, or an alternative transcript of similar size. These experiments demonstrate the presence of at least two isoforms of SPOCK-3 in stromal cells, most likely representing the primary 49 kDa transcript that exists in a glycosylated form and variant 005/N-Tes that can exist in both glycosylated and unglycosylated form (34–37 kDa). In contrast, only a single isoform is observed in β cells. The glycosylation detected by PNGase F treatment may well represent N-linked glycosaminglycan chains attached to non-consensus N-glycosylation motifs. N-linked glycosylation at non-consensus motifs are now known to occur in mammalian genomes97. Multiple high molecular weight bands (>90 kDa) were observed in PS-1 and β cell lysates at variable intensities, that are likely to reflect the addition of glycosaminoglycan chains (Suppl. Figure 2d). Mouse SPOCK-3 was recently shown to contain heparin sulphate proteoglycans, although N-linked glycosylation was not detected in mouse SPOCK-398. These experiments therefore demonstrate the novel finding that SPOCK-3 contains novel N-linked glycosylation sites.
As described above, the observation that two bands appear following de-glycosylation suggests the expression of two distinct core proteins, and is consistent with the presence of 005/N-Tes (~36 kDa) plus the full-length protein corresponding to the primary transcript or similar (~49 kDa) in PS-1 cells. However, other explanations are possible, including the presence of digestion products or differential post-translational modification in addition to N-linked glycosylation. We therefore sought to test whether distinct splice variant transcripts could be detected.
The exon structure of all 17 SPOCK-3 alternative splice variants banked in ENSEMBL was examined in order to design primers to detect variants. SPOCK-3 is unusual in that alternative splicing affects multiple regions across the entire coding sequence, as well as the 5′ UTR, suggesting that SPOCK-3 has a high degree of tolerance for variability within the protein structure80. Variants truncated at the 5′ end (201, 017, 202), at the 3′ end (005), and in internal regions (013, 010, 202, 018) are described in the database. As shown in Suppl. Figure 3, 19 exons are currently identified, the first 4 of which form the 5′ UTR. The 7 transcripts that encode proteins highly similar to the primary transcript are shown in blue. It can be seen that these variants differ primarily in the 5′ UTR exons, with 001/014, 002/015 and 006/16 pairs having identical coding sequences, differing only in the use of 5′ UTR exon 1/exon 2. In contrast, 012 uses 5′ UTR exon 4 which in fact contains an upstream translation start producing a predicted protein with an additional 12 amino acids at the N-terminus (translation performed using exPASY). However, it is not clear whether this start codon is used. Interestingly, exons 8 and 9 (as labelled in Suppl. Figure 3) are identical microexons of 9 bp. The coding sequences of 001, 014, 002 and 015 are therefore identical, and differ from 006/016 by only 3 amino acids. The significance of microexons is not fully understood, but they have been shown to have functional effects99,100, and have been previously identified in murine SPOCKs98. Since these 7 transcripts produce highly similar proteins, we focused on transcripts predicted to encode medium length (201, 013) and short (017, 010, 202, 005) proteins for experimental confirmation.
Specific RT-PCR primers were designed to each of these variants, with the exception of transcript 017 for which unique primers could not be designed. The primer locations are shown in Suppl. Figure 3 and the sequences and predicted product sizes given in Suppl. Table 4. Generic primers were designed that should size differentiate between transcript 201 and the remaining transcripts (GenA), and that should amplify all transcripts listed except for 005 and 010 (GenB). As shown in Fig. 8b, we detected the 005 transcript in PS-1 cells, and the specificity of the PCR product was confirmed by Sangar sequencing. Transcripts 010, 201 and 202 were not detected using the primers specific to these sequences. The generic primers GenA and GenB detected PCR products of the expected size, and specificity was confirmed by Sangar sequencing. Since the GenB primers could not amplify 005 this confirms the presence of at least one other transcript in addition to 005, most likely the primary variant. The sequence of the GenA PCR product revealed the absence of microexons 8 and 9, and the sequence was instead identical to variants 006/016 (which have identical CDS). We therefore demonstrate that pancreatic stellate cells express two distinct SPOCK-3 splice variants, 005/N-Tes and 006/016, corresponding to the deglycosylated ~34 and ~45 kDa proteins observed by western blot.
Isoforms of the SMOC proteins
Two distinct isoforms of SMOC-1 were identified, with highly cell type specific expression (Fig. 5 and Suppl. Table 1). The 65 kDa isoform was expressed uniquely in endothelial cells, while the 53 kDa isoform was present primarily in β cells. Interestingly, SMOC-1 was either not detected or only weakly detected in fibroblasts and stellate cells. Only two splice variants with complete CDS were identified by bioinformatics analysis and both encode for highly similar 48 kDa proteins (Suppl. Table 3 and Figure 6), suggesting that alternative splicing is unlikely to account for the two isoforms observed. However, SMOC-1 has 9 predicted glycosylation sites (Suppl. Table 2) and therefore alternative glycosylation is more likely to explain the two distinct isoforms identified, as suggested by PNGase digestion in studies elsewhere54,101,102. It will therefore be important to analyse the effect of alternative glycosylation on SMOC-1 protein function to understand the roles of distinct isoforms in endothelial cells and β cells.
For SMOC-2, three alternative transcripts were identified in ENSEMBL: transcripts 001 and 002 are predicted to encode proteins of similar molecular weight (~50 kDa) and with overall similar domain structure, with the exception of a truncated acidic domain in 001 (Suppl. Table 3 and Figure 6). In contrast, variant 201 is predicted to encode a small 14 kDa protein that lacks a signal peptide and any predicted functional domains. The coding region of variant 201 is in fact not overlapping with that of the primary transcript and is therefore likely to encode an intracellular protein of quite distinct function. SMOC-2 has been previously detected between 54 kDa and 60 kDa, and was shown to be glycosylated by PNGase digestion74,101.
SMOC proteins have been associated to many cancers and reported to be involved in cellular differentiation, cell-cycle progression and in regulating cell responses to the environment. However, SMOC proteins are largely unstudied in pancreatic diseases such as PDAC and diabetes. We have shown that SMOC-1 and SMOC-2 are widely expressed in the pancreas, and that specific SMOC-1 isoforms are expressed in endothelial cells and β cells. It will therefore be important to study the function of SMOC isoforms in these cells and in pancreatic disease.
Isoforms and expression of FSTL-1
Expression of FSTL-1 was the most highly specific of the SPARC family proteins. We detected strong expression of a single ~40 kDa isoform specifically in pancreatic stellate cells, with weaker expression in fibroblasts and endothelial cells (Fig. 5 and Suppl. Table 1). This is consistent with the stromal expression pattern and staining in basement membranes observed by immunohistochemistry (Fig. 4). We identified two alternative transcripts with complete CDS in ENSEMBL that are predicted to share the same functional domains except for a truncated acidic domain in variant 004 (Suppl. Table 3 and Figure 6). Both variants contain a signal peptide sequence and are therefore predicted to be secreted extracellular proteins. The molecular weight of the observed protein (40 kDa) is consistent with the predicted molecular weight of the primary transcript with minor post-translational modification such as glycosylation, as has been previously reported103. FSTL-1 is sometimes overlooked as a member of the SPARC family since it has the least structural and sequence homology to SPARC and it has been suggested that the calcium binding EF hand in FSTL-1 may be non-functional103. Our data shows that FSTL-1 is expressed by stromal cells within the pancreas with an expression pattern highly reminiscent of SPARC28, and is expressed at high levels specifically by pancreatic stellate cells. This suggests that FSTL-1 may play a related role to SPARC in pancreatic disease and that the function of FSTL-1 warrants further study.
Despite SPARC-like expression pattern, exogenous FSTL-1 does not regulate β cell growth or proliferation
Compared to other SPARC family proteins that we have shown to be highly expressed throughout islets and in β cells, FSTL-1 and SPARC are the only SPARC family proteins detected in stromal cells and not in β cells by western blotting and IHC (Figs 4 and 5 and ref. 28). Like SPARC, FSTL-1 has been shown to regulate signalling of the TGF-β superfamily and to regulate growth factor signalling28,39,60,61,104,105. We therefore tested whether FSTL-1 can similarly regulate β cell growth. INS-1 β cells were treated with rFSTL-1 over a period of 3 days. Cell growth was measured using the Incucyte Zoom live cell imaging system, and cell proliferation was measured by BrdU incorporation over the final 24 hour period. However, as shown in Fig. 9, the addition of exogenous FSTL-1 had no effect on the growth or proliferation rate of β cells. Despite a highly similar pattern of expression to SPARC, FSTL-1 is therefore unlikely to be directly involved in the regulation of islet growth and survival.
FSTL-1 inhibits cancer cell proliferation
Although we did not observe any change in the growth or proliferation of β cells in response to FSTL-1, previous reports have suggested that FSTL-1 can act as a tumour suppressor in breast and ovarian cancer63. We therefore examined the effect of FSTL-1 on pancreatic cancer cell growth and proliferation. The addition of rFSTL-1 was found to inhibit the growth (Fig. 10a & b) and proliferation (Fig. 10c) of pancreatic cancer cells. Western blotting revealed that FSTL-1 is only expressed by pancreatic stromal cells and not by cancer cells (Fig. 10d). However, both stellate cells and cancer cells express DIP2A (Fig. 10e), which acts as a receptor for FSTL-1106,107. Analysis of FSTL-1 immunohistochemistry data in the Human Cancer Atlas database shows that FSTL-1 is expressed at ‘medium’ levels in the normal pancreas but is not detected in the majority of pancreatic cancer tissues analysed108. Furthermore, FSTL-1 is similarly reduced compared to normal tissue in a range of other cancers including liver, breast, renal and stomach cancer108. Together, this data suggests that FSTL-1 produced by stromal cells normally acts to inhibit pancreatic cancer cell growth, and that FSTL-1 expression is downregulated within pancreatic tumours. Whether this difference is clinically significant would require further analysis that is outside the scope of this study. However, the data suggests that FSTL-1 is a novel tumour suppressor in pancreatic cancer. Furthermore, SPARC and FSTL-1 produced by stromal cells have opposing effects on pancreatic cancer cell growth, and it will therefore be of interest in future studies to test whether the combined signature of SPARC overexpression and FSTL-1 inhibition is useful diagnostically.
The SPARC family of matricellular proteins are important multifunctional regulators of cellular and matrix interactions. Our data shows that the extended SPARC family is expressed in pancreatic β cells, stromal cells and in ducts. We identified multiple isoforms with cell-type specific expression that arise from a complex mixture of post-translational modifications and expression of alternative splice variants. Furthermore, intracellular variants of the wider SPARC family were also identified, and these are likely to have distinct functions compared to secreted variants. We have further shown that FSTL-1 inhibits pancreatic cancer cell growth, suggesting that SPARC and FSTL-1 produced by stromal cells have antagonistic effects on cancer cell growth.
We have shown that taking a systematic and holistic approach to the study of the SPARC family of proteins and addressing the complexity of the different isoforms will be essential for understanding the function of these proteins and their role in health and disease, and is likely to represent an important challenge for the field. This study therefore provides a foundation for future research investigating the SPARC family in pancreatic diseases such as diabetes and cancer.
Pancreas sections for immunohistochemistry were obtained from adult male and female outbred ICR mice (21–25 g) from Harlan, Bicester, UK. Tissues were fixed in 10% NBF and embedded in paraffin. Animal maintenance was performed in accordance with the principles of laboratory animal care. No procedures covered by UK Home Office Regulations were carried out in this study.
Paraffin embedded sections (5 μm) of ICR pancreas were deparaffinised in histoclear (National Diagnostics) or histochoice (Amresco) and hydrated with 100% and 70% ethanol. Blocking was performed using 10% normal horse serum for 30 minutes in a humidified chamber. Antibodies to the SPARC family of proteins were selected to ensure that the epitope was either within the unique acidic domain I, or outside of any highly conserved domains. Full details of the antibodies used and concentrations are given in Suppl. Table 5. Primary antibodies were incubated overnight, followed by incubation with relevant biotinylated secondary antibody for 1 hour at room temperature. Antibody binding was detected using ABC peroxidase kit with DAB substrate (Vector Labs). Sections were counterstained with haematoxylin. Adjacent sections were stained in parallel with the relevant secondary antibody only as a negative control, and this was blank in all experiments. Digital images were acquired using a Nikon Eclipse 80i microscope and analysed using ImageJ software.
PS-1 pancreatic stellate cells and MRC5 fibroblast cells were kindly provided by Professor Hemant Kocher from the Barts Cancer Institute, Queen Mary University of London. AsPC-1, Hpaf, Capan-1, Panc-1 pancreatic cancer cells and INS-1 β cells were kindly provided by Dr. Charlotte Edling from the Blizzard Institute, Barts and the London. MIN-6 β cells were kindly provided by Professor Peter Jones of King’s College London. HUVEC endothelial cells were kindly provided by Dr. Andrew Snabaitis at Kingston University, London.
PS-1, AsPC-1, Hpaf, Capan-1, and Panc-1 cells were grown in RPMI-1640 media supplemented with 2 mM L-glutamine, 100 μg/ml penicillin and streptomycin, and 10% FBS (Gibco). INS-1 β cells were grown in RPMI-1640 supplemented with 2 mM L-glutamine, 100 μg/ml penicillin and streptomycin, 1 mM sodium pyruvate, 10 mM HEPES buffer, 0.05 mM β-mercaptoethanol and 10% FBS. MIN-6 β cells and MRC5 fibroblasts were grown in DMEM media supplemented with 100 μg/ml penicillin and streptomycin and 10% FBS. HUVEC cells were grown in F12K media supplemented with 100 μg/ml penicillin and streptomycin, 0.1 mg/ml heparin, 50 μg/ml ECGS (Millipore), and 10% FBS. Cells were incubated at 37 °C in 5% CO2.
Cell growth assays
INS-1 β-cells (1.5 × 104 cells/well) and AsPC-1 (5 × 103 cells/well) pancreatic cancer cells were plated in a 96 well plate and synchronised in low serum media (0.5% FBS) for 24 hrs. Post synchronisation, the cells were either provided with fresh untreated medium or with medium containing various concentrations of rFSTL-1 (R&D Systems) and cultured for further 72 hrs. Cell growth was monitored every 12 hrs during this period using the IncuCyteZOOM live cell imaging system (Essen Bioscience). BrdU incorporation (Roche Applied Science) was measured for the last 24 hrs of the 72 hr culture according to the manufacturer’s instructions. Statistical significance was calculated using Student’s t-test (unpaired, two-tailed) or one-way ANOVA and a p-value < 0.05 was considered significant.
Transfection complexes were formed using human SPARC siRNA (J-003710-10 Dharmacon) and HiPerFect (Qiagen) in serum-free medium for 20 minutes at room temperature. Human non-targeting siRNA was used as a control (Dharmacon). During this period PS-1 cells were plated at a density of 1 × 105 cells per well in a 24 well plate. Transfection reagents were then added to the cells to give a final concentration of 80 nM siRNA. Transfection was carried out for 48 hours and knockdown was confirmed by western blot with SPARC antibody. Hevin isoforms were then detected using antibodies specific to the N- and the C-terminus (see Suppl. Table 5 for antibody details).
Protein expression analysis by Western Blot
Cells were lysed with RIPA buffer (Sigma Aldrich) for 20 minutes on ice in the presence of protease inhibitors (HaltTM Protease Inhibitor Single Use Cocktail). Lysates were subsequently cleared by centrifugation and the supernatant collected. Samples were run immediately after lysis to avoid potential issues with protein degradation86. For glycosylase experiments, cell lysates were denatured at 100 °C for 4 minutes then incubated with PNGase-F for one hour at 37 °C according to the manufacturer’s instructions (New England BioScience).
Protein concentration was determined using the BCA protein assay (Bio-Rad DC). Sample buffer was added to lysates after which equal protein was loaded onto 12% polyacrylamide gels and subjected to SDS-PAGE (20–25 μg of protein/well). Proteins were then transferred onto nitrocellulose membranes and blocked with 5% milk solution. Membranes were incubated overnight at 4 °C with the relevant rabbit SPARC family primary antibody (see Suppl. Table 5) and mouse β-actin antibody (1:2500, Abcam) then washed with Tween TBS. Anti-rabbit and anti-mouse secondary antibodies conjugated respectively to IR800 and IR700 infra-red dyes were used for detection. Membranes were visualised by infrared using a Li-Cor Odyssey CLx scanner. Molecular weight and signal intensity was measured using Li-Cor Image Studio. Image processing of greyscale images for figure preparation was limited to changes in brightness and contrast applied to the entire blot, and in some cases the image was flipped to invert the order, or the order of the wells changed for clarity and consistency. In all cases the images shown are an accurate representation of the original data. Cropped blots are used in the main paper and the full uncropped blots are shown in supplementary data. Statistical significance was calculated using Student’s t-test (unpaired, two-tailed) and a p-value < 0.05 was considered significant.
mRNA expression analysis by RT-PCR
Total RNA was isolated from PS-1 cells using an RNeasy Mini Kit, including on-column DNase I treatment (Qiagen). Total RNA was quantified using a NanoVue™ Plus Spectrophotometer and RNA integrity confirmed using an Agilent Bioanalyzer 2100. RNA (700 ng) was reverse transcribed to cDNA using a RevertAid First Strand cDNA Synthesis Kit (ThermoFisher Scientific). PS-1 cDNA was amplified using DreamTaq Green PCR Master Mix (ThermoFisher Scientific). Primers were designed to SPOCK-3 splice variants banked in ENSEMBL (Accessed March 2013) using PrimerBLAST (See Suppl. Table 4 and Suppl. Figure 3). Primer sequences used for DIP2A were: Forward primer- GCAGATGGTGTCCCTGTGAAC Reverse primer- CTGATTTGGATCTGGTTGCTGA. At least one primer in each pair was designed to be exon spanning to avoid amplification of any residual genomic template. RT-PCR products were separated on a 2% agarose gel in TAE. QARS primers (for-TTCCGGTGTCTCTGCAATGG; rev- CTGCTGAGCCTGAGTAGCG) were used as a loading/positive control. All negative controls were blank (no RT cDNA, no template cDNA, and PCR dH20 control).
The ENSEMBL database was used to identify alternative splice variants of the human SPARC family of proteins. Only protein-coding transcripts for which the complete coding sequence (CDS) is known were included in the analysis. For these transcripts, protein FASTA sequences were downloaded. The ENSEMBL transcript IDs used are given in Suppl. Table 3 [download date April 2015]. Respective product sizes for each complete transcript were calculated using the Protein Molecular Weight Bioinformatic tool from the Sequence Manipulation Suite. Domain structures for alternative transcripts were determined using the InterPro protein sequence analysis and classification database. Signal peptide expression was determined using Phobius signal peptide predictor. Genecards, UNIPROT, Phosphosite plus, and TRANSDAB were used to identify predicted post-translational modifications of the SPARC family (primary variants). The Human Protein Atlas was accessed July 2016.
How to cite this article: Viloria, K. et al. A holistic approach to dissecting SPARC family protein complexity reveals FSTL-1 as an inhibitor of pancreatic cancer cell growth. Sci. Rep. 6, 37839; doi: 10.1038/srep37839 (2016).
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Weir, G. C. & Bonner-Weir, S. Islet β cell mass in diabetes and how it relates to function, birth, and death. Ann. N. Y. Acad. Sci. 1281, 92–105 (2013).
International Diabetes Federation. IDF Diabetes Atlas, 7 ed. http://www.idf.org/idf-diabetes-atlas-seventh-edition (2015).
Ferlay, J., Soerjomataram, I., Ervik, M., Dikshit, R., Eser, S., Mathers, C., Rebelo, M., Parkin D. M., Forman, D. & Bray, F. GLOBOCAN 2012 v1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11. http://globocan.iarc.fr (2013).
Virtanen, I., Banerjee, M., Palgi, J., Korsgren, O., Lukinius, A., Thornell, L. E., Kikkawa, Y., Sekiguchi, K., Hukkanen, M., Konttinen, Y. T. & Otonoski, T. Blood vessels of human islets of langerhans are surrounded by a double basement membrane. Diabetologia 51, 1181–1191 (2008).
Otonoski, T., Banergee, M., Korsgren, O., Thornell, L. E. & Virtanen, I. Unique basement membrane structure of human pancreatic islets: implications for β-cell growth and differentiation. Diabetes, Obesity, and Metabolism 10, 119–127 (2008).
Stendhal, J. C., Kaufman, D. B. & Stupp, S. I. Extracellular matrix in pancreatic islets: relevance to scaffold design and transplantation. Cell Transplant 18, 1–12 (2009).
Jalili, R. B., Rezakhanlou, A. M., Hosseini-Tabatabaei, A., Ao, Z., Warnock, G. L. & Ghahary, A. Fibroblast populated collagen matrix promotes islet survival and reduced the number of islets required for diabetes reversal. Journal of Cellular Physiology 226, 1813–1819 (2010).
Zhang, Y., Jalili, R. B., Warnock, G. L., Ao, Z., Marzban, L. & Ghahary, A. Three-dimensional scaffolds reduce islet amyloid formation and enhance survival and function of cultured human islets. The American Journal of Pathology 181, 1296–1305 (2012).
Diaferia, G., Jimenez-Caliani, A., Ranjitkar, P., Yang, W., Hardiman, G., Rhodes, C., Crisa, L. & Cirulli, V. β1 integrin is a crucial regulator of pancreatic-cell expansion. Development 140, 3360–3372 (2013).
Riopel, M., Krishnamurthy, M., Li, J., Liu, S., Leask, A. & Wang, R. Conditional β1-integrin-deficient mice display impaired pancreatic β cell function. Journal of Pathology 224, 45–55 (2011).
Bachem, M. G., Schneider, E., Gross, H., Weidenbach, H., Schmid, R. M., Menke, A., Siech, M., Beger, H., Grunert, A. & Adler, G. Identification, culture, and characterization of pancreatic stellate cells in rats and humans. Gastroenterology 115, 421–432 (1998).
Bachem, M. G., Schunemann, M., Ramadani, M., Siech, M., Beger, H., Buck, A., Zhou, S., Schmid-Kotsas, A. & Adler, G. Pancreatic carcinoma cells induce fibrosis by stimulating proliferation and matrix synthesis of stellate cells. Gastroenterology 128, 907–921 (2005).
Apte, M. V., Haber, P. S., Applegate, T. L., Norton, I. D., McCaughan, G. W., Korsten, M. A., Pirola, R. C. & Wilson, J. S. Periacinar stellate shaped cells in rat pancreas: identification, isolation, and culture. Gut 43, 128–133 (1998).
Ellenrieder, V., Alber, B., Lacher, U., Hendler, S. F., Menke, A., Boeck, W., Wagner, M., Wilda, M., Friess, H., Buchler, M., Adler, G. & Gress, T. M. Role of MT-MMPs and MMP-2 in pancreatic cancer progression. International Journal of Cancer 85, 14–20 (2000).
Mahadevan, D. & Von Hoff, D. D. Tumor-stroma interactions in pancreatic ductal adenocarcinoma. Molecular Cancer Therapeutics 6, 1186–1197 (2007).
Bilder, D., Li, M. & Perrimon, N. Cooperative regulation of cell polarity and growth by drosophila tumor suppressors. Science 289, 113–116 (2000).
Radisky, D., Hagios, C. & Bissell, M. J. Tumors are unique organs defined by abnormal signaling and context. Seminars in Cancer Biology 11, 87–95 (2001).
Cox, T. R. & Erler, J. T. Remodelling and homeostasis of the extracellular matrix: implications for fibrotic diseases and cancer. Disease Models & Mechanisms 4, 165–178 (2011).
Hezel, A. Kimmelman, A. C., Stranger, B. Z., Bardeesy, N. & DePinho, R. A. Genetics and biology of pancreatic ductal adenocarcinoma. Genes & Development 20, 1218–1249 (2006).
Neese, A., Michl, P., Frese, K. K., Feig, C., Cook, N., Jacobetz, M. A., Lolkema, M. P., Buchholz, M., Olive, K. P., Gress, T. M. & Tuveson, D. A. Stromal Biology and therapy in pancreatic cancer. Gut 60, 861–868 (2010).
Lunardi, S., Muschel, R. & Brunner, T. The stromal compartments in pancreatic cancer: Are there any therapeutic targets? Gut 343, 147–155 (2014).
Murphy-Ullrich, J. E. & Sage, E. H. Revisiting the matricellular concept. Matrix Biology 37, 1–14 (2014).
Bradshaw, A. Diverse biological functions of the SPARC family of proteins. International Journal of Biochemsitry and Cell Biology 44, 480–488 (2012).
Raines, E. W., Lane, T. F., Iruela–Arispe, M. L., Ross, R. & Sage, E. H. The extracellular glycoprotein SPARC interacts with platelet derived growth factor (PDGF)-AB and -BB and inhibits the binding of PDGF to its receptors. Proc Natl Acad Sci 89, 1281–1285 (1992).
Kupprion, C., Motamed, K. & Sage, E. H. SPARC inhibits the mitogenic effect of vascular endothelial growth factor on microvascular endothelial cells. J Biol Chem 273, 29635–29640 (1999).
Hasselaar, P. & Sage, E. H. SPARC antagonizes the effect of bFGF on the migration of bovine aortic endothelial cells. J Cell Biochem 49, 272–283 (1992).
Motamed, K. et al. Fibroblast growth factor receptor-1 mediates the inhibition of endothelial cell proliferation and the promotion of skeletal myoblast differentiation by SPARC: A role for protein kinase A. Journal of Cellular Biochemistry 90, 408–423 (2003).
Ryall, C., Viloria, K., Lhaf, F., Walker, A., King, A., Jones, P., Mackintosh, D., McNeice, R., Kocher, H., Flodstrom-Tullberg, M., Edling, C. & Hill, N. Novel Role for Matricellular Proteins in the Regulation of Islet β Cell Survival. Journal of Biological Chemistry 289, 30614–30624 (2014).
Schiemann, B. J., Neil, J. R. & Schiemann, W. P. SPARC Inhibits Epithelial Cell Proliferation in Part through Stimulation of the Transforming Growth Factor-Signaling System. Molecular Biology of the Cell 14, 3977–3988 (2003).
Chlenski, A. et al. SPARC enhances tumor stroma formation and prevents fibroblast activation. Oncogene 26, 4513–4522 (2007).
Weaver, M. S., Workman, G. & Sage, E. H. The copper binding domain of SPARC mediates cell survival in vitro via interaction with integrin beta1 and activation of integrin-linked kinase. J. Biol. Chem. 283, 22826–22837 (2008).
Rentz, T. J., Poobalarahi, F., Bornstein, P., Sage, E. H. & Bradshaw, A. D. SPARC regulates processing of procollagen I and collagen fibrillogenesis in dermal fibroblasts. J Biol Chem 282, 22062–22071 (2007).
Bradshaw, A. D. et al. SPARC-null mice display abnormalities in the dermis characterized by decreased collagen fibril diameter and reduced tensile strength. J Invest Dermatol 120, 949–955 (2003).
Rivera, L. B., Bradshaw, A. D. & Brekken, R. A. The regulatory function of SPARC in vascular biology. Cellular and Molecular Life Sciences 68, 3165–3173 (2011).
Trombetta-eSilva, J. & Bradshaw, A. D. The function of SPARC as a mediator of fibrosis. The Open Rheumatology Journal 6, 146–155 (2012).
Guweidhi, A. et al. Osteonectin influences growth and invasion of pancreatic cancer. Ann Surg 242, 224–234 (2005).
Mantoni, T. S. et al. Stromal SPARC expression and patient survival after chemoradiation for non-resectable pancreatic adenocarcinoma. Cancer Biology & Therapy 7, 1806–1815 (2008).
Wu, D., Li, L., Yang, M., Liu, H. & Yang, G. Elevated plasma levels of SPARC in patients with newly diagnosed type 2 diabetes mellitus. Eur J Endocrinol 165, 597–601 (2011).
Xu, L. et al. Elevated Plasma SPARC Levels Are Associated with Insulin Resistance, Dyslipidemia, and Inflammation in Gestational Diabetes Mellitus. PloS One 8, p.e81615 (2013).
Kos, K. et al. Regulation of the fibrosis and angiogenesis promoter SPARC/osteonectin in human adipose tissue by weight change, leptin, insulin, and glucose. Diabetes 58, 1780–1788 (2009).
Harries, L. W. et al. A role for SPARC in the moderation of human insulin secretion. PloS One 8, e68253 (2013).
Sullivan, M. M. et al. Matricellular Hevin regulates decorin production and collagen assembly. Journal of Biological Chemistry 281, 27621–27632 (2006).
Girard, J. P. & Springer, T. A. Cloning from purified high endothelial venule cells of hevin, a close relative of the antiadhesive extracellular matrix protein SPARC. Immunity 2, 113–123 (1995).
Brekken, R. A. et al. Expression and characterization of murine Hevin (SC1), a member of the SPARC family of matricellular proteins. Journal of Histochemistry and Cytochemistry 52, 735–748 (2004).
Hambrock, H. O. et al. SC1/Hevin an extracellular calcium-modulated protein that binds collagen I. Journal of Biological Chemistry 278, 11351–11358 (2003).
Weaver, M. et al. Proteolysis of matricellular protein Hevin by matrix metalloproteinase-3 produces a SPARC-like fragment (SLF) associated with neovasculature in a murine glioma model. Journal of Cellular Biochemistry 112, 3093–3102 (2011).
Weaver, M., Workman, G., Cardo-Vila, M., Arap, W. & Pasqualini, R. & Sage, E. H. Processing of matricellular protein Hevin in mouse brain is dependent on ADAMTS4. Journal of Biological Chemistry 285, 5868–5877 (2010).
Nakada, M. et al. Suppression of membrane-type 1 matrix metalloproteinase (MMP)-mediated MMP-2 activation and tumor invasion by Testican 3 and its splicing variant gene product, N-Tes. Canc 61, 8902 (2001).
Nakada, M., Miyamori, H., Yamashita, J. & Sato, H. Testican 2 abrogates inhibition of membrane-type matrix metalloproteinases by other Testican family proteins. Cancer Res 63, 3364–3369 (2003).
Kessenbrock, K., Plaks, V. & Werb, Z. Matrix metalloproteinases: regulators of the tumor microenvironment. Cell 141, 52–67 (2010).
Damhofer, H. et al. Assessment of the stromal contribution to Sonic Hedgehog-dependent pancreatic adenocarcinoma. Molecular Oncology 7, 1031–1042 (2013).
Miao, L. et al. SPOCK1 is a novel transforming growth factor-β target gene that regulates lung cancer cell epithelial-mesenchymal transition. Biochemical and Biophysical Research Communications 440, 792–797 (2013).
Thomas, J. T., Canelos, P., Luyten, F. P. & Moos, M. Jr. Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus. J. Biol. Chem. 284, 18994–19005 (2009).
Choi, Y. A. et al. Secretome analysis of human BMSCs and identification of SMOC1 as an important ECM protein in osteoblast differentiation. Journal of Proteome Research 9, 2946–2956 (2010).
Brellier, F. et al. SMOC1 is a tenascin-C interacting protein over-expressed in brain tumors. Matrix Biology 30, 225–233 (2011).
Fackler, M. J. et al. Genome-wide methylation analysis identifies genes specific to breast cancer hormone receptor status and risk of recurrence. Cancer Res 71, 6195–6207 (2011).
Shvab, A. et al. Induction of the intestinal stem cell signature gene SMOC-2 is required for L1-mediated colon cancer progression. Oncogene (2015).
Rocnik, E. F., Liu, P., Sato, K., Walsh, K. & Vaziri, C. The novel SPARC family member SMOC-2 potentiates angiogenic growth factor activity. Journal of Biological Chemistry 281, 22855–22864 (2006).
Maier, S., Paulsson, M. & Hartmann, U. The widely expressed extracellular matrix protein SMOC-2 promotes keratinocyte attachment and migration. Experimental Cell Research 314, 2477–2487 (2008).
Shibanuma, M., Mashimo, J., Mita, A., Kuroki, T. & Nose, K. Cloning from a mouse osteoblastic cell line of a set of transforming-growth-factor-β1-regulated genes, one of which seems to encode a follistatin-related polypeptide. Eur J Biochem 217, 13–19 (1993).
Tsuchida, K. et al. Identification and characterization of a novel follistatin-like protein as a binding protein for the TGF-β family. Journal of Biological Chemistry 275, 40788–40796 (2000).
Kudo-Saito, C., Fuwa, T., Murakami, K. & Kawakami, Y. Targetting FSTL1 prevents tumor bone metastasis and consequent immune dysfunction. Cancer Res 73, 6185–6193 (2013).
Chan, Q. K. et al. Tumor suppressor effect of follistatin-like 1 in ovarian and endometrial carcinogenesis: a differential expression and functional analysis. Carcinogenesis 30, 114–121 (2009).
Kutsukake, M. et al. Circulating IGF-binding protein 7 (IGFBP7) levels are elevated in patients with endometriosis or undergoing diabetic hemodialysis. Reprod Biol Endocrinol 54(6).
Gu, H. F. et al. Evaluation of IGFBP-7 DNA methylation changes and serum protein variation in Swedish subjects with and without type 2 diabetes. Clin Epigenetics 5, 20 (2013).
An, W. et al. Low expression of IGFBP7 is associated with poor outcome of pancreatic ductal adenocarcinoma. Annals of surgical oncology 19, 3971–3978 (2012).
Mukherjee, A. et al. FSTL3 deletion reveals roles for TGF-beta family ligands in glucose and fat homeostasis in adults. Proc. Natl. Acad. Sci. USA 104, 1348–1353 (2007).
Iruela–Arispe, M. L. et al. Expression of SPARC during development of the chicken chorioallantoic membrane: evidence for regulated proteolysis in vivo. Mol Biol Cell 6, 327–343 (1995).
Clezardin, P. et al. Complex formation of human thrombospondin with osteonectin. Eur J Biochem 175, 275–284 (1988).
Sawyer, A. J. & Kyriakides, T. R. Matricellular proteins in drug delivery: Therapeutic targets, active agents, and therapeutic localization. Adv. Drug Deliv. Rev. (2016).
The Human Protein Atlas. http://www.proteinatlas.org/ (2016).
Esposito, I. et al. Tumor-suppressor function of SPARC-like protein 1/Hevin in pancreatic cancer. Neoplasia 9, 8–17 (2007).
Hausser, H., Decking, R. & Brenner, R. E. Testican-1, an inhibitor of pro-MMP-2 activation, is expressed in cartilage. Osteoarthritis and cartilage 12, 870–877 (2004).
Vannahme, C., Gosling, S., Paulsson, M., Maurer, P. & Hartmann, U. Characterization of SMOC-2, a modular extracellular calcium-binding protein. Biochem. J. 373, 805–814 (2003).
Lane, T. F. & Sage, E. H. The biology of SPARC, a protein that modulates cell-matrix interactions. J. FASEB 8, 163–173 (1994).
Shinohara, M. L., Kim, H. J., Kim, J. H., Garcia, V. A. & Cantor, H. Alternative translation of osteopontin generates intracellular and secreted isoforms that mediate distinct biological activities in dendritic cells. Proc. Natl. Acad. Sci. USA 105, 7235–7239 (2008).
Aeschlimann, D., Kaupp, O. & Paulsson, M. Transglutaminase-catalyzed matrix cross-linking in differentiating cartilage: identification of osteonectin as a major glutaminyl substrate. J. Cell Biol. 129, 881–892 (1995).
Arjomandi, M. et al. Secreted osteopontin is highly polymerized in human airways and fragmented in asthmatic airway secretions. PloS One 6 (2011).
BaSalamah, M. A., Marr, H. S., Duncan, A. W. & Edgell, C. S. Testican in Human Blood 1. Biochem. Biophys. Res. Commun. 283, 1083–1090 (2001).
Viloria, K. & Hill, N. J. Embracing the complexity of matricellular proteins: the functional and clinical significance of splice variation. Biomolecular concepts 7, 117–132 (2016).
McClung, H. M. et al. Deletion of the SPARC acidic domain or EGF-like module reduces SPARC-induced migration and signaling through p38 MAPK/HSP27 in glioma. Carcinogenesis 33, 275–284 (2012).
Bertrand, S. et al. A dynamic history of gene duplications and losses characterizes the evolution of the SPARC family in eumetazoans. Proc. Biol. Sci. 280, 20122963 (2013).
Kawasaki, K., Suzuki, T. & Weiss, K. M. Genetic basis for the evolution of vertebrate mineralized tissue. Proc. Natl. Acad. Sci. USA 101, 11356–11361 (2004).
Novinec, M., Kordis, D., Turk, V. & Lenarcic, B. Diversity and evolution of the thyroglobulin type-1 domain superfamily. Mol. Biol. Evol. 23, 744–755 (2006).
Martinek, N., Shahab, J., Sodek, J. & Ringuette, M. Is SPARC an evolutionarily conserved collagen chaperone? J. Dent. Res. 86, 296–305 (2007).
Bendik, I., Schraml, P. & Ludwig, C. U. Characterization of MAST9/Hevin, a SPARC-like protein, that is down-regulated in non-small cell lung cancer. Cancer Res 58, 626–629 (1998).
CsoHosz, Mesk’o Bertalan & F’esus, L. Transdab wiki: the interactive transglutaminase substrate database on web 2.0 surface. Amino Acids 36, 615–617 (2009).
Hohenadl, C. et al. Two adjacent N-terminal glutamines of BM-40 (osteonectin, SPARC) act as amine acceptor sites in transglutaminaseC-catalyzed modification. J. Biol. Chem. 270, 23415–23420 (1995).
Lau, C., Poon, R., Cheung, S., Yu, W. & Fan, S. SPARC and Hevin expression correlate with tumour angiogenesis in hepatocellular carcinoma. J. Pathol. 210, 459–468 (2006).
Gao, J. et al. Research Methylation of the SPARC gene promoter and its clinical implication in pancreatic cancer. (2010).
Barker, T. H. et al. Matricellular homologs in the foreign body response: hevin suppresses inflammation, but hevin and SPARC together diminish angiogenesis. The American journal of pathology 166, 923–933 (2005).
Bonnet, F., Perin, J., Maillet, P., Jolles, P. & Alliel, P. M. Characterization of a human seminal plasma glycosaminoglycan-bearing polypeptide. Biochem. J. 288, 565–569 (1992).
Headey, S. J. et al. C-terminal domain of insulin-like growth factor (IGF) binding protein-6: structure and interaction with IGF-II. Molecular Endocrinology 18, 2740–2750 (2004).
Bevec, T., Stoka, V., Pungercic, G., Dolenc, I. & Turk, V. Major histocompatibility complex class II-associated p41 invariant chain fragment is a strong inhibitor of lysosomal cathepsin L. J. Exp. Med. 183, 1331–1338 (1996).
Lenarcic, B. et al. Saxiphilin, a saxitoxin-binding protein with two thyroglobulin type 1 domains, is an inhibitor of papain-like cysteine proteinases. J. Biol. Chem. 275, 15572–15577 (2000).
Meh, P., Pavšič, M., Turk, V., Baici, A. & Lenarčič, B. Dual concentration-dependent activity of thyroglobulin type-1 domain of testican: specific inhibitor and substrate of cathepsin L. Biol. Chem. 386, 75–83 (2005).
Schwarz, F. & Aebi, M. Mechanisms and principles of N-linked protein glycosylation. Curr. Opin. Struct. Biol. 21, 576–582 (2011).
Hartmann, U. et al. Testican‐3: a brain‐specific proteoglycan member of the BM‐40/SPARC/osteonectin family. J. Neurochem. 125, 399–409 (2013).
Volfovsky, N., Haas, B. J. & Salzberg, S. L. Computational discovery of internal micro-exons. Genome Res. 13, 1216–1221 (2003).
Saffell, J. L., Walsh, F. S. & Doherty, P. Expression of NCAM containing VASE in neurons can account for a developmental loss in their neurite outgrowth response to NCAM in a cellular substratum. J. Cell Biol. 125, 427–436 (1994).
Liu, P., Lu, J., Cardoso, W. V. & Vaziri, C. The SPARC-related factor SMOC-2 promotes growth factor-induced cyclin D1 expression and DNA synthesis via integrin-linked kinase. Molecular Biology of the Cell 19, 248–261 (2008).
Vannahme, C. et al. Characterization of SMOC-1, a novel modular calcium-binding protein in basement membranes. J. Biol. Chem. 277, 37977–37986 (2002).
Hambrock, H. O. et al. Structural characterization of TSC-36/Flik: analysis of two charge isoforms. J. Biol. Chem. 279, 11727–11735 (2004).
Dong, Y. et al. Blocking follistatin-like 1 attenuates bleomycin-induced pulmonary fibrosis in mice. J. Exp. Med. 212, 235–252 (2015).
Geng, Y. et al. Follistatin-like 1 (Fstl1) is a bone morphogenetic protein (BMP) 4 signaling antagonist in controlling mouse lung development. Proc. Natl. Acad. Sci. USA 108, 7058–7063 (2011).
Tanaka, M. et al. DIP2 disco‐interacting protein 2 homolog A (Drosophila) is a candidate receptor for follistatin‐related protein/follistatin‐like 1–analysis of their binding with TGF‐β superfamily proteins. FEBS journal 277, 4278–4289 (2010).
Ouchi, N. et al. DIP2A functions as a FSTL1 receptor. J. Biol. Chem. 285, 7127–7134 (2010).
The Cancer Genome Atlas - National Cancer Institute. http://cancergenome.nih.gov/ (2016).
We would like to thank Dr. Aileen King and Professor Peter Jones at King’s College London for assistance in obtaining pancreas tissue, Dr. Ruth Kirk at Kingston University for assistance with immunohistochemistry, colleagues who provided cell lines used in this study, and members of the laboratory for useful discussions. This work was funded by the IhSHA research hub at Kingston University.
The authors declare no competing financial interests.
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Viloria, K., Munasinghe, A., Asher, S. et al. A holistic approach to dissecting SPARC family protein complexity reveals FSTL-1 as an inhibitor of pancreatic cancer cell growth. Sci Rep 6, 37839 (2016). https://doi.org/10.1038/srep37839
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