Pancreatic beta cells are of great interest for biomedical research and regenerative medicine. Here we show the conversion of human fibroblasts towards an endodermal cell fate by employing non-integrative episomal reprogramming factors in combination with specific growth factors and chemical compounds. On initial culture, converted definitive endodermal progenitor cells (cDE cells) are specified into posterior foregut-like progenitor cells (cPF cells). The cPF cells and their derivatives, pancreatic endodermal progenitor cells (cPE cells), can be greatly expanded. A screening approach identified chemical compounds that promote the differentiation and maturation of cPE cells into functional pancreatic beta-like cells (cPB cells) in vitro. Transplanted cPB cells exhibit glucose-stimulated insulin secretion in vivo and protect mice from chemically induced diabetes. In summary, our study has important implications for future strategies aimed at generating high numbers of functional beta cells, which may help restoring normoglycemia in patients suffering from diabetes.
Generation of functional pancreatic insulin-producing beta cells for the effective treatment of diabetes is a key area of translational research. Stepwise differentiation protocols have been devised to guide the differentiation of human embryonic stem cells (hESCs)1, and more recently induced pluripotent stem cells (iPSCs)2, into definitive endoderm, primitive gut tube endoderm, posterior foregut endoderm and pancreatic endoderm (PE). These hESC-derived PE cells can mature into functional beta-like cells in vivo after prolonged periods following transplantation into immunodeficient mice3,4,5. More recently, improved differentiation protocols have been described that allow the formation of functional beta-like cells from hESCs under cell culture conditions6,7,8. While these findings are encouraging, several challenges remain and significant efforts have been directed towards further improvement of differentiation conditions9,10,11,12,13, the expansion of cells at different progenitor stages14,15 and the purification of target cell populations16 to obtain sufficient quantities of functional pancreatic beta cells.
An alternative strategy previously employed is the conversion of fibroblasts towards lineage-specific proliferative progenitors in vitro17,18,19. The benefit of such an approach is the ability to generate large numbers of cells suitable for any downstream assays and applications before final differentiation into the desired cell type in vitro or in vivo. We previously devised a Cell-Activation and Signalling-Directed (CASD) lineage conversion strategy, which employs transient overexpression of iPSC-transcription factors in conjunction with lineage-specific soluble signals to reprogramme somatic cells into diverse lineage-specific cell types without first establishing a pluripotent state20,21. Using this method, we and other groups have demonstrated the successful reprogramming of fibroblasts and other cells into cardiac cells22,23, neural progenitors24,25,26, angioblast-like progenitors27, endothelial cells28 and hepatocytes29. In addition, we recently demonstrated the generation of functional pancreatic beta-like cells from mouse fibroblasts using the CASD strategy30. However, successful translation of these approaches to generate functional human beta-like cells from fibroblasts that are capable of reversing diabetes in mouse models has not been demonstrated so far.
Here we demonstrate that human endodermal progenitor cells can be established from neonatal and adult human fibroblasts in vitro by employing a non-integrating reprogramming approach following the CASD transdifferentiation paradigm. We have identified conditions that allow great expansion of converted cells at distinct progenitor stages, including posterior foregut and PE. Converted pancreatic endodermal progenitors can be induced to efficiently differentiate into glucose-responsive beta-like cells in vitro. Beta-like cells transplanted into surrogate mice are functional in vivo and possess the ability to protect mice from diabetes. Therefore, these findings suggest an approach for the potential production of patient-specific insulin-producing cells to study relevant and unresolved questions in beta-cell biology.
Converting fibroblasts into endodermal progenitor cells
Human foreskin fibroblasts were transduced with non-integrating episomal reprogramming factors, OCT4, SOX2, KLF4 and a short hairpin RNA against p5331, recovered in fibroblast medium for 4 days, and cultured in initiation medium containing epidermal growth factor (EGF), basic fibroblast growth factor (bFGF) and CHIR99021 (an activator of WNT signalling) to support cell proliferation (Fig. 1a). After 7 days, the culture conditions were switched to endodermal conversion media containing high level of Activin A (100 ng ml−1) and CHIR99021 to establish converted definitive endodermal progenitor (cDE) cells, based on previous studies demonstrating key roles for the Activin A and WNT signalling pathways in endodermal fate decision in vitro and in vivo32,33,34. This basic endodermal conversion protocol gave rise to cell colonies with an epithelial morphology between days 21 to 28 (Fig. 1b). Colonies specifically stained for definitive endodermal progenitor markers SOX17 and FOXA2, but not for the pluripotency marker NANOG or primitive gut markers HNF6 and HNF4α (Fig. 1c; Supplementary Fig. 1a). As expected, control fibroblasts were negative for endodermal and pluripotency markers (Supplementary Fig. 1a). To increase the efficiency of our endodermal conversion protocol, we performed a small-scale screening of chemical compounds covering bioactive molecules capable of controlling cell fate35. We observed that combined addition of the epigenetic modulators: sodium butyrate (NaB, a histone deacetylase inhibitor), Parnate (Par, a histone demethylase inhibitor) and RG108 (RG, a DNA methylase inhibitor) could significantly improve the conversion efficiency by 2.5-fold (Fig. 1a,d). Additional screening using this improved condition revealed that 5′-N-ethylcarboxamidoadenosine (NECA, an adenosine agonist) could further increase the conversion rate by 2-fold, resulting in a 5-fold increase over the basal protocol (Fig. 1d). Notably, by employing this optimized condition, we could generate ∼50 FOXA2 and SOX17 double-positive cDE colonies from 400,000 human fibroblasts (Fig. 1d). Quantitative PCR (qPCR) analysis revealed that mRNA expression of fibroblast-specific markers, THY1 and COL1A1, was rapidly downregulated during the first 7 days of reprogramming, suggesting a rapid dedifferentiation process (Supplementary Fig. 1b). Endodermal gene transcripts, SOX17 and FOXA2, were gradually upregulated (Fig. 1e). In contrast, the expression of endogenous pluripotency gene transcripts NANOG and OCT4 remained at very low levels during the conversion process (Fig. 1e; Supplementary Fig. 1c). Taken together, these data demonstrate that human fibroblasts can be converted into cDE cells using an episomal reprogramming system by employing the CASD transdifferentiation approach.
Characterization of posterior foregut-like progenitor cells
Next, we attempted to serially expand the number of cDE colonies via treatment with media containing two small molecules, the WNT signalling activator CHIR99021 and the TGFβ signalling inhibitor A83-01 in conjunction with two growth factors EGF and bFGF that significantly promoted their expansion (Fig. 2a,b). Immunofluorescence analysis revealed strong expression of endodermal progenitor markers SOX17 and FOXA2, but also induction of primitive gut tube marker HNF4α and posterior foregut marker HNF6 (Fig. 2c), suggesting further specification towards posterior foregut-like progenitor cells (cPF cells). Employing these culture conditions, we established five cPF cell lines from four independent experiments employing human neonatal fibroblasts (Fig. 2d). cPF cells proliferated rapidly with an average doubling time of 2 days for up to 15 passages (Fig. 2e,g). All four media supplements were important for cPF cell self-renewal (Fig. 2f) and expanded cPF cells maintained their epithelial colony morphology, as well as posterior foregut-like phenotype as determined by immunofluorescence staining for SOX17, FOXA2, HNF4α, HNF6 and SOX9 (Fig. 2g,h; Supplementary Figs 2–4). During mouse embryonic development, Pdx1 expression is first detected at embryonic day 8.5 and marks the endodermal region that will give rise to the whole pancreas, as well as the common bile duct, distal stomach and duodenal epithelium36,37. Interestingly, we detect PDX1 protein (Fig. 2h). Consistently, qPCR analysis demonstrated the induced high-level expression of multiple posterior foregut progenitor gene transcripts, including SOX17, FOXA2, HNF1A, HNF1B, HNF4A, HNF6, SOX9 and PDX1 in cPF cells when compared with parental fibroblasts (Fig. 2i). In contrast, ectodermal marker gene SOX1, mesodermal marker gene BRACHYURY, and pluripotency marker genes OCT4 and NANOG were not induced (Fig. 2i). Collectively, these data confirm the specific posterior foregut identity of cPF cells, which is further supported by our observations that cPF cells at both early and late passages possessed comparable capacities to differentiate towards the hepatic lineage (Supplementary Fig. 5b). Of note, cPF cells can be frozen and thawed with a recovery rate of 82.7±5.1% (n=3), an important advantage enabling many downstream assays. We further checked the genome stability of cPF cells using comparative genomic hybridization arrays and did not observe any gross chromosomal aberrations, but detected four copy number variants in one human neonatal fibroblast-derived cPF cell line (Supplementary Fig. 6). This result is consistent with a recent report demonstrating that long-term cultures of bipotent stem cells from adult human liver are genome stable38. Notably, the episomal reprogramming vectors were spontaneously lost in established cPF cell lines (Supplementary Fig. 5a), thus overcoming a current safety concern associated with the integration of viral vector-based reprogramming/conversion approaches. Another potential safety concern regarding cells with proliferative and stem cell capacity is their potential for tumour formation39. Transplantation of expanded cPF cells under the kidney capsule of immunodeficient mice did not result in tumour formation even after prolonged periods up to 24 weeks in vivo (n=10) (Supplementary Fig. 5c). In contrast, all controls (hESC-derived endodermal progenitor cell populations) formed tumorigenic structures with big cysts and increased graft size 7 weeks after transplantation (n=4) (Supplementary Fig. 5c). Haematoxylin and eosin staining of cPF grafts showed epithelial structures (Supplementary Fig. 5d) and further immunofluorescence analysis demonstrated protein expression of characteristic endodermal markers, including E-cadherin, HNF4α, PDX1, SOX9 and pan-cytokeratin (Fig. 2j). In summary, our results demonstrate that cPF cells can be greatly expanded in culture while maintaining their posterior foregut endodermal phenotype.
Characterization of pancreatic endodermal progenitor cells
Recently, several studies have reported the use of small molecules and growth factors to achieve differentiation of hESC-derived primitive gut tube and posterior foregut endoderm into pancreatic endoderm3,4,11,40. Using a similar approach7,8, we screened different combinations of small molecules and growth factors to differentiate cPF cells into more committed pancreatic endodermal progenitor cells (cPE cells). We optimized a two-step protocol in which cPF cells were first exposed to FGF7, FGF10, A83-01, Compound-E (an inhibitor of Notch signalling), retinoic acid (RA), GDC-0449 (an antagonist of Sonic hedgehog) and LDN-193189 (an inhibitor of BMP4 signalling) for 2 days (Fig. 3a). Subsequently, differentiating cells were treated with EGF, Exendin-4 (an agonist of glucagon (GCG)-like peptide-1), A83-01, LDN-193189, PBDu (an activator of protein kinase C), Compound-E and Nicotinamide (an inhibitor of polyADP-ribose synthetase) for another 3 days (Fig. 3a). Resulting cPE cells continued to express high levels of FOXA2, HNF6, SOX9 and PDX1, as expected41,42 (Fig. 3b). Most importantly, this treatment resulted in the generation of PDX1 and NKX6.1 double-positive cells (Fig. 3c). NKX6.1 expression in common PDX1-positive pancreatic progenitors (before NKX6.1 expression becomes further restricted to beta cells) marks their commitment to a more specific endocrine-/ductal-bi-potent progenitor cell type43. Notably, hESC-derived PDX1 and NKX6.1 double-positive PE progenitor cells have been shown to be able to give rise to functional beta cells after transplantation16. Fluorescence-activated cell sorting (FACS) analysis revealed approximately 78% of PDX1-positive cells, and 17.3% PDX1 and NKX6.1 double-positive cells within cPE populations at passage 1 (Fig. 3d). The level of NKX6.1 expression detected in cPE cells is comparable to PE cells differentiated from hESCs as described by more conventional means (Supplementary Fig. 7a). Next, we tested the cPF expansion media on cPE cultures in an attempt to expand cPE cells in a similar manner. However, cPE colonies easily detached from the plate under cPF expansion condition. Omission of CHIR99021 and increasing the EGF concentration to 50 ng ml−1 reversed this effect and promoted cPE cell expansion (Fig. 3f). Employing this optimized culture condition, cPE cells were expanded with an approximate doubling time of 3 days for up to 14 passages (Fig. 3e). Of note, expanded cPE cells maintained their progenitor identity as evidenced by the presence of PDX1 and NKX6.1 double-positive cells at passage 12 (Fig. 3g). Consistently, qPCR results demonstrated the downregulation of early endodermal marker gene SOX17. The pan-endodermal marker genes FOXA2 and HNF4A, as well as many pancreatic and endocrine marker genes, including HNF6, PTF1A, HLXB9 and NGN3, were upregulated (Fig. 3h). More robust expression was noted for other markers, including PDX1, NKX2.2 and NKX6.1, which are also highly expressed in mature beta cells.
To explore whether expanded cPE cells can further mature into functional beta cells in vivo, we transplanted cPE cells under the kidney capsule of immunodeficient mice. After 15–16, 19–20 and 23–24 weeks, we detected human C-peptide after a glucose challenge in the blood of 62.5%, 75% and 86.6% of mice analysed, respectively, albeit at low levels (Fig. 3i). In addition, we detected a 2.1-fold increase in human C-peptide in the serum of mice-bearing 23-week-old grafts after glucose challenge when compared with fasting levels, illustrating that cPE grafts gave rise to functional beta-like cells on transplantation into host animals (Fig. 3j). Starting at 15 weeks post transplantation, we found insulin-expressing beta-like cells and PDX1-positive pancreatic progenitor cells in some graft sections, while other regions were negative for pancreatic markers (Fig. 3k). Insulin-positive cells co-expressed the critical beta-cell transcription factors PDX1 and NKX6.1, but did not show expression of other endocrine hormones (Fig. 3k). In addition, we detected CK19-positive duct-like structures, but not Amylase-positive exocrine cells, a finding that supports the notion that cPE cells possess bi-potential duct/endocrine progenitor capacity (Supplementary Fig. 7b). In summary, our data demonstrates that cPF cells can be differentiated into cPE cells, which can be greatly expanded in vitro while maintaining their specific phenotype. Importantly, cPE cells differentiate further in vivo towards insulin-producing, single-hormonal cells capable of releasing insulin in response to glucose challenge.
Maturation of cPE cells into pancreatic beta-like cells
To address the question of whether cPE cells can develop into functional beta-like cells under cell culture conditions, we first incubated cPE cells in a basal pancreatic differentiation media that has been shown to promote hESC/iPSC-derived pancreatic progenitor differentiation into insulin-producing cells40. This media includes A83-01, Nicotinamide, Forskolin (an activator of adenylyl cyclase), Dexamethasone (an agonist of glucocorticoid receptor) and Exendin-4 (Fig. 4a). While we consistently observed C-peptide-positive cells expressing high levels of PDX1 after 10–14 days in culture (Fig. 4b), the relatively low number (∼0.5%) suggested that further optimization was required. Chemical compounds able to promote differentiation of definitive endoderm44 and PDX1-positive progenitors9 have been identified previously. However, discovering molecules directing the final steps of differentiation into beta-like cells has been challenging due to difficulties in generating and maintaining sufficient numbers of differentiation-competent PE cells. We performed a chemical screen45 with the intent of identifying factors that would result in more efficient development of C-peptide-positive cells from expanded cPE cells. These experiments revealed that supplementation of the basal pancreatic differentiation media individually with Compound-E (an inhibitor of Notch signalling), Vitamin C or BayK-8644 (a Ca2+ channel agonist) were effective in increasing the percentage of C-peptide-positive cells (Fig. 4c). Combined treatment with these compounds had an additive effect (Exendin-4, A83-01, Nicotinamide, Forskolin, Dexamethasone, Compound-E, Vitamin C and BayK-8644), resulting in the formation of up to 7% C-peptide-positive cells (Fig. 4c).
Previously, insulin-producing cells generated from ESCs/iPSCs are mostly immature as evidenced by co-expression of endocrine hormones, the lack of crucial beta-cell transcription factors and the inability to secrete insulin in response to physiological levels of glucose46. The maturation defects may be partly due to the lack of three-dimensional (3D) organization normally present in islets of Langerhans47. Hence, we generated free-floating cell aggregates of cPE cells that first had been incubated as 2D cultures for 10 days in the improved maturation media (protocol 1). The majority of cells within the aggregates expressed the pan-pancreas marker PDX1 after 8–12 days of 3D culture (Fig. 4d; Supplementary Fig. 8a,b). In addition, we detected many insulin-expressing cells co-expressing key beta-cell transcription factors, including PDX1, NKX6.1, NKX2.2 and NEUROD1 (Fig. 4d; Supplementary Fig. 8b). In contrast, insulin-expressing cells only rarely co-stained for the endocrine progenitor marker NGN3 or other endocrine hormones, including GCG and somatostatin (SST) (Fig. 4d; Supplementary Fig. 8b). Of note, all insulin-positive cells also stained for a human-specific C-peptide antibody, thus excluding possible insulin uptake from the media (Supplementary Fig. 8c). Considering the expression of key beta-cell markers, we designate these cells as converted pancreatic beta-like cells (cPB cells). One of the distinguishing hallmarks of pancreatic beta cells is the ability to release insulin upon glucose stimulation. Importantly, glucose-stimulated insulin secretion (GSIS) assays demonstrated that in vitro-generated cPB cells released insulin in response to physiological levels of glucose (n=7, fold increase 2.1±1.3) (Fig. 4e). Collectively, our findings illustrate the generation of functional pancreatic beta-like cells that respond to physiological levels of glucose in vitro.
cPB cells protect mice from STZ-induced diabetes
Functional insulin-producing cells are capable of regulating glucose levels in surrogate animals. Unfortunately, our initial trials in which cPB cells (protocol 1) were transplanted into immunocompromised, streptozotocine (STZ)-treated diabetic mice were unsuccessful, with most animals retaining high glucose levels and eventually succumbing to diabetes without recovery. Encouraged by two recent papers that introduced improved protocols for pancreatic differentiation7,8, we further improved the maturation conditions of cPE cells into cPB cells (protocol 2) (Fig. 5a). In addition to the Notch inhibitor that we already employed in protocol 1 and that was also included in both published protocols, we tested whether the addition of Vitamin C and BayK-8644, which were discovered during our initial chemical screens, had additional beneficial effects. We found that both compounds promoted expression of the INSULIN gene (Fig. 5b) as well as increased the number of C-peptide-positive cells co-expressing key beta-cell transcription factors PDX1 and NKX6.1 (Fig. 5c). C-peptide-positive cells rarely co-stained for other endocrine hormones, including GCG and SST (Fig. 5c). Quantitative FACS analysis revealed the formation of about 15% monohormonal C-pep+GCG-SST- cells, with only few polyhormonal cells (Figs 5d,e). We infected cPE cells with a lentivirus containing a minimal insulin promoter driving a fluorescence reporter expression and FACS-sorted cPB cells at d21 (Fig. 5g). qPCR analysis for the expression of beta-cell marker genes, including INS, PDX1, NKX6.1, NKX2.2, NEUROD1, PAX6, RFX6, MAFA, GCK, PCSK1, KIR6.2, SUR1, UCN3 and SLC30A8 of sorted cPB cells in comparison to human islets showed comparable levels for most genes, with only few genes showing slightly reduced levels of expression (Fig. 5h).
GSIS assays conducted with in vitro-generated cPB cells revealed a robust release of insulin in response to physiological levels of glucose (n=7, fold increase 2.0±0.4) (Fig. 5f; Supplementary Fig. 9a). The stimulation index, as calculated by the ratio of insulin secreted in high glucose to low glucose, was similar among the cPB cells, hESC-derived beta-like cells and primary human islets6,7,8. Thus, our findings illustrate that protocol 2 efficiently generates functional pancreatic beta-like cells in vitro.
Considering these major improvements for in vitro-generated cPBs, we decided to re-evaluate their in vivo function by transplanting cPB cells into immunodeficient mice (Fig. 6a). Importantly, while control human fibroblasts did not evoke any response, we detected significant glucose-stimulated insulin secretion in cPB-transplanted mice 2 months after transplantation (Fig. 6b; Supplementary Fig. 9b). Immunofluorescence analysis of cPB grafts revealed the presence of many islet-like structures containing insulin-expressing pancreatic beta-like cells. C-peptide-positive cells co-expressed critical beta-cell transcription factors PDX1 and NKX6.1, but did not exhibit expression of other endocrine hormones GCG and SST (Fig. 6c). Specific ablation of the endogenous beta cells by the toxin STZ resulted in rapid onset of overt diabetes in all control animals, while cPB-bearing mice remained euglycemic (Fig. 6d). 5 weeks post-STZ treatment, cPB grafts were removed by uni-lateral nephrectomy. Nephrectomized mice rapidly developed diabetes, demonstrating that human fibroblast-derived cPB cells controlled glucose levels in STZ-treated mice. In summary, these results directly demonstrate that cPB cells transplanted into surrogate mice are functional in vivo and protect mice from diabetes.
Generating pancreatic beta-like cells from adult human fibroblasts
We applied our pancreatic conversion strategy to adult human fibroblasts and established six cPF cell lines from three independent experiments that were further expanded. Using the same culture conditions as for neonatal fibroblast-derived progenitors, we were able to generate expandable cPF and cPE cells from adult fibroblasts (Supplementary Fig. 10a,b). We checked the genome stability of cPF cells using comparative genomic hybridization arrays and did not observe any gross chromosomal aberrations, but only one copy number variant in one adult fibroblast-derived cPF cell line (Supplementary Fig. 11), indicating their genome stability. cPE cells could further differentiate into pancreatic beta-like cells at efficiencies comparable to neonatal fibroblast-derived cPB cells, with only few double hormone-positive cells (Supplementary Fig. 12a–c). Most importantly, human adult fibroblast-derived cPB cells are functional as demonstrated by their glucose-stimulated insulin secretion (Supplementary Fig. 12d). While results from the analysis of neonatal and adult fibroblast-derived pancreatic cells are remarkably similar, we do acknowledge certain batch-to-batch variation among experiments; a finding that mirrors prior reports observing variations among primary adult beta-cell preparations and stem cell-derived beta-like cells6,7,8. Therefore, our results demonstrate that human adult fibroblasts can be used to efficiently and rapidly generate functional cPB cells, a finding that opens up opportunities for patient-specific analysis of beta-cell properties and cell therapy approaches.
Various strategies towards the generation of functional beta cells are currently being pursued, including directed differentiation of pluripotent stem cells2,3,4,6,7,8 and direct reprogramming of different endodermal cell types48,49,50,51. In this study, we (I) developed a simple, robust and non-integrating approach for the inter-lineage conversion of mesodermal human fibroblasts into definitive endodermal progenitor cells (cDE cells) following the CASD transdifferentiation approach; (II) showed that cDE cells could be further specified into posterior foregut-like progenitor (cPF) cells that can be greatly expanded; (III) demonstrated that cPF cells can be further differentiated into expandable pancreatic endodermal progenitor (cPE) cells; (IV) reported that these cPE cells can give rise to functional pancreatic beta-like (cPB) cells in vitro; (V) and demonstrated that transplanted cPB cells exhibit glucose-stimulated insulin secretion in vivo and protect mice from chemically induced diabetes.
By following the CASD transdifferentiation paradigm17,18,21, we show that conversion of fibroblasts into proliferative progenitor populations with the ability to give rise to beta cells represents an attractive and feasible approach for the generation of vast numbers of human beta cells under cell culture conditions. The current efficiency of the conversion process is low and we expect higher yields on future improvements similar to those previously accomplished for iPSC reprogramming45. While the approach is robust, the individual roles of reprogramming factors as ‘pioneer transcription factors’ and the detailed analysis of the underlying molecular mechanisms of the conversion process require more systematic investigations52,53,54. Employing transient expression of iPSC- reprogramming factors31 under the CASD approach, likely establishes a permissive state in cells, that can be exploited by incubation in culture conditions previously shown to favour definitive endoderm derivation32,33,34. This notion is supported by the observation that addition of epigenetic chemical modulators significantly increased the conversion efficiency.
Notably, the resulting cDE cells could rapidly be specified towards the posterior foregut state (cPF), suggesting efficient transdifferentiation of the fibroblasts towards the endodermal germ layer. Subsequently, we established cPF cell lines that can be greatly expanded without loss of their specific identity. This kind of virtually unlimited expansion is reminiscent of the recently described generation and expansion of endodermal progenitor cells from hESCs (eEP)14. However, eEP cells have been described as definitive endodermal progenitors while our established cPF cells resemble a further specified posterior foregut-like cell type. The difference in developmental stage might be explained by the different expansion conditions for cPF cells, relying solely on activation of the WNT pathway and inhibition of the TGFβ pathway in combination with pro-proliferative growth factors EGF and bFGF. A somewhat unexpected finding was the observation that we can expand not only cPF cells, but also cPE cells committed towards a pancreatic phenotype. The expansion of cPE cells by at least two hundred million fold involved the addition of a selective set of factors, including bFGF, EGF and compound A83-01. A role for EGF in short-term proliferation of hESC-derived PE cells has been suggested previously2,55. Interestingly, we found that inhibition of the TGFβ pathway by A83-01 was particularly important for the expansion process of cPE cells, a finding that correlates well with prior reports showing that inhibition of TGFβ signalling is beneficial for pancreatic specification of differentiating hESCs11. Mechanistically, inhibition of TGFβ signalling might promote epithelial cell proliferation while at the same time interfering with the commonly observed culture induced epithelial-to-mesenchymal transition process56. It would be particularly interesting to test whether the cPE expansion conditions we identified can also be employed to amplify hESC-derived PE cells in a similar manner. Future in-depth analysis of our endodermal progenitor populations and their comparison with progenitor cells generated by distinct methods, such as eEP cells or hESC-derived PE cells, will provide invaluable information about the mechanisms underlying endodermal progenitor specification and self-renewal in a human setting that has remained hard to study due to the limited supply of embryonic samples at the relevant stages.
Importantly, employing a chemical library screen on expanded cPE cells in vitro resulted in the discovery of several small molecules, including the Notch inhibitor Compound-E, Vitamin C and the Ca2+ channel agonist BayK-8644 that could improve the differentiation efficiency into pancreatic beta-like cells independently as well as in combination. Notch inhibition in bi-potent PE cells induces expression of NGN3, a factor essential for endocrine cell development57,58, and similar findings have recently been reported for conventional hESC to beta-cell differentiation protocols7,8. The effects of Vitamin C and BayK-8644 on beta-cell differentiation have been less well-studied. Of note, our group described previously that Vitamin C was effective in promoting mouse pancreatic beta-cell differentiation and maturation30. Recent reports suggested Vitamin C is involved in many epigenetic modifications, including DNA and histone demethylation59, promotes cell fate conversion60 and improves cell quality61,62. Therefore, future studies will explore the roles of Vitamin C and related epigenetic regulators in pancreatic differentiation and maturation63,64,65. With regard to the functional properties of BayK-8644, one very attractive underlying mechanism could be related to the Ca2+/Calcineurin (Cn)/Nuclear Factor-Activated T cells (NFAT) signalling pathway, known to promote mouse and human pancreatic beta-cell proliferation and maturation66,67,68. More detailed analysis of the mechanistic functions of these compounds in future studies might reveal novel properties of pancreatic beta-cell differentiation and function that could be exploited for cell therapy approaches.
Significantly, our in vitro-differentiated beta-like cells exhibit a functional beta-cell phenotype as judged by their ability to secrete insulin in response to physiological levels of glucose, as well as their co-expression of critical beta-cell transcription factors. While we observed a similar fold change in human C-peptide secretion on glucose stimulation of cPB cells in comparison to recently described hESC-derived beta-like cells and human islets, we note a wider range of secretion, similar to what has been reported for iPSC-derived beta-like cells7,8. Further, in-depth analysis may reveal additional genes and epigenetic modifiers that regulate the maturation process of pancreatic beta cells from somatic cells. Nonetheless, even in its present state our findings clearly indicate the potential of human adult fibroblast-derived functional beta-like cells for the identification and analysis of novel patient-specific properties of these insulin-producing cells.
Finally, the transplantation experiments of cPB cells into immunodeficient mice highlight their ability to give rise to functional islet-like structures in this physiological context. This is in contrast to human iPSC-derived pancreatic beta-like cells which, despite their ability to respond to glucose-stimulated insulin secretion in vitro and in vivo, have not been reported to be able to protect immunocompromised mice from STZ-induced diabetes on transplantation7,8. Thus, our studies represent one of the few examples of human cell types generated through cellular reprogramming that could protect against or even cure an existing disease19.
We are cognizant of the fact that our cPB cell cultures do not contain all cells typically found in human islets, including mesenchymal support cells, endothelial cells, and neural cells. Thus, even while we observe clear evidence for the functional properties of the fibroblast-derived beta-like cells, we anticipate that future co-culture experiments aimed at fully replicating the cellular composition of human islets will further optimize the function of cPB cells. Furthermore, there is likely an in vivo maturation process of in vitro-engineered pancreatic cells, as reported in recent studies of hESC-derived pancreatic beta cells7,8, whose underlying mechanisms have not been fully elucidated yet. We anticipate that understanding the signals that guide beta-cell maturation will allow generating human fibroblast-derived cells fully recapitulating all properties of human pancreatic beta cells.
In summary, our study demonstrates an effective conversion strategy for human fibroblasts into the endodermal lineage, describes robust expansion conditions for distinct endodermal progenitor cell populations and identifies novel cocktails of signalling factors that promote the successful differentiation of these endodermal progenitor cells into functional beta-like cells both in vitro and in vivo. Most significantly, when transplanted into immunocompromised mice, these cPB cells produced human insulin and protected mice from diabetes. We surmise that the current CASD strategy is a viable alternative to commonly used iPSC approach and that these efforts will advance our understanding of basic pancreas biology and disease modelling, as well as the development of cell replacement therapies and drug testing strategies.
Conversion of human fibroblasts into endodermal progenitor cells
Human foreskin fibroblasts (CRL-2097, ATCC) and adult human dermal fibroblasts (Cell Applications) were cultured in a 10-cm tissue-culture dish in regular fibroblast culture medium. Reprogramming with episomal vectors was done as described31. Briefly, 4 × 105 fibroblasts were electroporated with up to 6 μg of episomal vectors (pCXLE-hOCT3/4-shp53-F, pCXLE-hSK and pCXLE-EGFP) using the Microporator Human Dermal Fibroblast (NHDF) Nucleofector Kit (Lonza) according to the manufacturer's instructions. Cells were cultured in fibroblast medium for 4 days and then re-plated onto Matrigel-coated 10-cm dishes at a density of 50 000 cells per dish. The cells were then cultured in reprogramming initiation medium (DMEM/F12, 10% Knockout serum replacement, 5% ES-FBS, 1% Glutamax, 1% Non-essential amino acids, 1% penicillin/streptomycin, 0.1 mM β-mercaptoethanol, 10 ng ml−1 bFGF, 10 ng ml−1 EGF, 2 μM Par, 0.5 μM RG, 0.1 mM NaB, 0.5 μM NECA and 3 μM CHIR99021) for 1 week, followed by endodermal induction medium (Advanced RPMI, 2% ES-FBS, 1% Glutamax, 1% Non-essential amino acids, 1% penicillin/streptomycin, 0.1 mM β-mercaptoethanol, 2 μM Par, 0.5 μM RG, 0.1 mM NaB, 0.5 μM NECA, 3 μM CHIR99021 and 100 ng ml−1 Activin A) for another 2–3 weeks. The converted colonies were carefully picked up for expansion in expansion medium (DMEM, 1% Glutamax, 0.5 × N2, 0.5 × B27, 5 μg ml−1 BSA, 1% penicillin/streptomycin, 10 ng ml−1 bFGF, 10 ng ml−1 EGF, 0.5 μM A83-01 and 3 μM CHIR99021) and were passaged at 1:4–1:6 each time by Accutase treatment. Routinely, 0.5 μM thiazovivin was used during the first 12–24-h period of each passage to prevent cell death after dissociation. All cell culture products were from Invitrogen/Gibco BRL and all chemicals and growth factors were from Stemgent except where mentioned.
Differentiation of cPF cells into cPE cells
For pancreatic differentiation, cPF cells were cultured in pancreatic differentiation medium (DMEM, 1% Glutamax, B27, 5 μg ml−1 BSA, 1% penicillin/streptomycin) with 25 ng ml−1 FGF7, 25 ng ml−1 FGF10, 0.5 μM A83-01, 0.1 μM Compound-E, 2 μM RA, 0.1 μM GDC-0449 and 0.1 μM LDN-193189 for 2 days; then 50 ng ml−1 EGF, 50 ng ml−1 Exendin-4, 0.5 μM A83-01, 0.1 μM Compound-E, 50 nM TPB, 0.1 μM LDN-193189 and 10 mM nicotinamide for another 3 days. After differentiation, the cPE cell population was passaged with Accutase and cultured in cPE expansion medium (DMEM, 1% Glutamax, 1 × B27, 5 μg ml−1 BSA, 1% penicillin/streptomycin, 10 ng ml−1 bFGF, 50 ng ml−1 EGF and 0.5 μM A83-01). Routinely, 0.5 μM thiazovivin was used during the first 12–24 h period of each passage to prevent cell death after dissociation.
Maturation of cPE cells into cPB cells
Protocol 1. The cPE cells were differentiated into beta-like cells in the pancreatic maturation media with DMEM, 1% Glutamax, B27, 5 μg ml−1 BSA and 1% penicillin/streptomycin, 50 ng ml−1 Exendin-4, 1 μM A83-01, 10 μM forskolin, 10 μM dexamethasone, 10 mM nicotinamide, 0.1 μM Compound-E, 50 μg ml−1 Vitamin C and 2 μM BayK-8644 for 10 days, and then cultured as 3D aggregates in low-attachment plates for another 8–12 days.
Protocol 2. The cPE cells were differentiated into beta-like cells in the pancreatic maturation media with DMEM, 1% Glutamax, B27, 5 μg ml−1 BSA and 1% penicillin/streptomycin, 10 μg ml−1 Heparin, 10 μM ZnSO4, 10 μM Alk5 inhibitor II, 0.1 μM LDN-193189, 1 μM T3, 0.1 μM Compound-E, 2 μM BayK-8644, 0.25 mM Vc for 7d; and DMEM, 1% Glutamax, B27, 5 μg ml−1 BSA and 1% penicillin/streptomycin, 10 μg ml−1 Heparin, 10 μM ZnSO4, 10 μM Alk5 inhibitor II, 1 μM T3, 1 mM N-cysteine, 10 μM Trolox, 2 μM R428, 2 μM BayK-8644 and 0.25 mM Vc for 7 days, and then cultured as 3D aggregates in low-attachment plates for another 7 days.
Standard immunostaining was carried out as previously reported69. For cell cluster staining, primary and secondary antibodies were incubated overnight at 4 °C. Secondary antibodies were Alexa Fluor-conjugated (1:500–1,000) (Invitrogen). Nuclei were visualized by Hoechst (Sigma-Aldrich) staining. Images were captured using a Nikon Eclipse TE2000-U microscope or a SP5 confocal microscope. The primary antibodies used are detailed in Supplementary Table 1. A representative picture of at least five independent experiments is shown in Figs 1b,c and 2g,h. A representative picture of at least three independent experiments is shown in Figs 2c,j, 3b,c,g, 4b and 5c and Supplementary Figs 2–4. A representative picture of three independent experiments is shown in Supplementary Figs 1a, 5b, 8b,c, 10a,b and 12a. A representative image of two independent mice is shown in Figs 3k and 6c and Supplementary Fig. 7b.
Cells were harvested at the indicated time points by Accutase treatment, fixed with 4% formaldehyde solution, and washed five times with ice-cold Perm/Wash buffer (BD). Cells were aliquoted and incubated individually or combinatory with antibodies and isotype controls on ice for 2 h. Cells were washed with Perm/Wash buffer for five times and incubated individually with Alexa Fluor 488-conjugated or Alexa Fluor 555-conjugated antibodies (1:500, Invitrogen) on ice for 1 h. Cells were washed with Perm/Wash buffer for five times, re-suspended in 0.5 ml ice-cold PBS with 2% FBS and analysed by FACSCalibur and CellQuest software (BD). FlowJo software (Tree Star) was used to analyse the data.
For qPCR analysis, total RNA was extracted using the RNeasy Plus Mini Kit in combination with QIAshredder (Qiagen). First strand reverse transcription was performed with 1 μg RNA using iScript cDNA Synthesis Kit (Bio-Rad). qPCR was taken out using iQ SYBR Green Supermix (Bio-Rad). The primers used are detailed in Supplementary Table 2.
Kidney capsule transplantation
Mice (NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ mice, NSG mice, The Jackson Laboratory) used in this study were maintained according to protocols approved by the University of California, San Francisco, Committee on Laboratory Animal Resource Center. The kidney capsule transplantation was done as previously reported70. Briefly, cells were collected from culture dishes by cell scraper, and injected under the renal capsule of immunodeficient NSG male mice (6–10-week-old). For transplantation assays of established cPF cell lines, hESC-derived definitive endoderm generated by differentiation for 1 day in RPMI containing 100 ng ml−1 Activin A and 50 ng ml−1 WNT3a, followed by 4 days in RPMI containing 0.2% FBS and 100 ng ml−1 Activin A served as a control. Grafts were dissected and analysed at the indicated time points. For in vivo functional assays of cPB cells, ∼5.0 × 106 cPB cells and control human fibroblasts were transplanted. For glucose-induced insulin secretion, mice were fasted overnight and serum was collected before and after i.p. administration of 3 g kg−1 D-glucose solution. For induction of diabetes, mice were administered 35 mg kg−1 Streptozotocin via i.p. injection for 5 days.
Glucose-stimulated insulin secretion
Cell were pre-incubated for 1 h in Krebs–Ringer buffer (KRB), followed by incubation for 1 h in KBR containing 2.8 mM glucose followed by 1 h incubation in KRB containing 16.7 mM glucose followed by 30 min in KRB containing 16.7 mM glucose and 30 mM KCl. Human C-peptide levels were quantified using an ultrasensitive ELISA kit (Mercodia; cross-reactivity with insulin and pro-insulin, 0.0006% and 1.8%, respectively).
Indicated P values were obtained using a two-tailed t-test, and all quantitative data are shown as mean±s.e.m. No statistical method was used to predetermine sample size. No samples were excluded. The experiments were not randomized. The investigators were not blinded to allocation during the experiments and outcome assessment.
How to cite this article: Zhu, S. et al. Human pancreatic beta-like cells converted from fibroblasts. Nat. Commun. 7:10080 doi: 10.1038/ncomms10080 (2016).
We thank members of the Hebrok and Ding laboratories for comments and discussion. S.Z. is a Gladstone/CIRM scholar. H.A.R was supported by a Richard G. Klein fellowship and a JDRF fellowship (3-2012-266). Image acquisition was supported by the microscopy core of the University of California, San Francisco Diabetes and Endocrinology Research Center (DERC, P30 DK63720). Research in the lab of MH is supported by grants from the NIH (DK089541, DK105831), a gift from Bruce Braden, and the Leona M. & Harry B. Helmsley Charitable Trust. S.D. is supported by funding from California Institute for Regenerative Medicine, NICHD, NHLBI, NEI, NIMH/NIH, Prostate Cancer Foundation, and the Gladstone Institute.
Supplementary Figures 1-12 and Supplementary Tables 1-2.
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Nature Reviews Gastroenterology & Hepatology (2017)