The stem cell niche has a strong influence in the differentiation potential of human pluripotent stem cells with integrins playing a major role in communicating cells with the extracellular environment. However, it is not well understood how interactions between integrins and the extracellular matrix are involved in cardiac stem cell differentiation. To evaluate this, we performed a profile of integrins expression in two stages of cardiac differentiation: mesodermal progenitors and cardiomyocytes. We found an active regulation of the expression of different integrins during cardiac differentiation. In particular, integrin α5 subunit showed an increased expression in mesodermal progenitors, and a significant downregulation in cardiomyocytes. To analyze the effect of α5 subunit, we modified its expression by using a CRISPRi technique. After its downregulation, a significant impairment in the process of epithelial-to-mesenchymal transition was seen. Early mesoderm development was significantly affected due to a downregulation of key genes such as T Brachyury and TBX6. Furthermore, we observed that repression of integrin α5 during early stages led to a reduction in cardiomyocyte differentiation and impaired contractility. In summary, our results showed the link between changes in cell identity with the regulation of integrin α5 expression through the alteration of early stages of mesoderm commitment.
The adult mammalian heart has a limited regenerative capacity, which is not enough to compensate for the extensive cell death that takes place during heart injuries1. In recent years, there have been major advances in the differentiation efficiency of cardiomyocytes derived from pluripotent stem cells (PSC)2. In this sense, one of the main long-term goals of de novo cardiomyocyte production is to provide a robust source of donor cells for regenerative therapies.
Not only does the stem cell niche play a key role in the growth and maintenance of pluripotency but it also has an important influence in the stem cell differentiation potential, including in cardiac differentiation3,4. Although embryonic tissue patterning can be partly regulated by the composition of the extracellular matrix (ECM), it is not completely understood how cell to ECM interactions are involved in the process of cardiac differentiation5. Central to these interactions are integrins, a superfamily of cell adhesion receptors that recognize different ECM proteins and that ultimately lead to the activation of signaling pathways which modify many cellular functions.
Integrins are composed of αβ transmembrane heterodimers; so far, eighteen α and eight β subunits have been described in humans6,7. Integrins are involved in modifying both adhesion and stiffness of several types of stem cells, which together with their active signaling function regulate PSC differentiation8. Previous studies have identified that α1β1, α5β1 and α7β1 are the most highly expressed integrin heterodimers in adult cardiomyocytes. They are predominantly collagen, fibronectin and laminin-binding receptors, respectively8. It has also been found that integrin α5 (Iα5) subunit is prevalent in fetal cardiomyocytes9, and that deletion of Iα5 subunit leads to mesodermal defects during mouse embryogenesis10,11. However, one of the challenges when studying integrins lies in that many of them have multiple ECM ligands and each ECM protein has multiple integrin receptors, even though each integrin heterodimer has higher specificity for specific ligands. We therefore hypothesized that specific integrins in human PSC might be involved in cardiac differentiation.
Here we found that the repression of Iα5 during early stages led to a significant impairment in EMT process and in early mesoderm development giving rise to a low cardiac differentiation efficiency and even a decreased contractility. We believe that determining the role of integrin subunits during cardiac differentiation could shed light into the mechanisms of cardiac differentiation, ultimately leading to higher differentiation efficiencies and its eventual application in regenerative medicine.
Cardiac differentiation models recapitulate early embryonic events
We first analyzed the differentiation stages of cardiac commitment in order to identify key time points of this process. After 3 days of mesoderm induction in a monolayer-cardiac differentiation protocol, we found a distinct cell population marked by the acquisition of CD56 (Fig. S1). We and others have previously shown that this cell population corresponds to early mesodermal progenitor cells (MPC)12,13. In addition, we observed an upregulation of key transcriptional regulators of the epithelial-to-mesenchymal transition (EMT), including Zeb-1 and Zeb-2, and a downregulation of e-Cadherin (Fig. S1). These results indicate that this cell population is actively undergoing EMT, a key process that occurs during embryonic patterning. To monitor the efficiency of cardiac differentiation, we used a reporter hESCs cell line that expresses eGFP under the control of the cardiac specific gene NKX2-514. Using this cell line, we found that 67.5 ± 4.6% of cells were NKX2-5/eGFP(+) at day 15 of differentiation (Fig. S1). Furthermore, mRNA analysis of the cardiac marker Myosin Heavy Chain, α isoform (α-MHC) and mRNA and protein analysis of cardiac Troponin T (cTnT) also exhibited a significant up-regulation (Fig. S1). At this stage, cardiomyocytes acquired a typical structure of contractile network easily identified by the expression of eGFP reporter (Fig. S1) (Online Movie I). We also performed the same analyses in a 3D-cardiac differentiation protocol and found similar results (Fig. S2).
Integrin expression during cardiac differentiation
Next, we analyzed the expression of several integrin subunits during cardiac differentiation, including Iα3, Iα4, Iα5, Iα6, Iα8, and Iβ1. These integrins are mostly involved in fibronectin and laminin signaling, which are ECM proteins that have been previously implicated in mesodermal specification. We found that Iα3, Iα4 and Iα6 were initially downregulated in early mesodermal progenitor cells but returned to basal levels at the cardiomyocyte stage (Figs. 1 and S3). Iα5 subunit showed a different regulation, with a significantly increased expression in mesodermal progenitors cells, while showing a significant reduction both in mRNA and protein level in cardiomyocytes at day 15. Iα8 mRNA increased significantly throughout cardiac differentiation but we could not detect a significant difference in the protein expression. Finally, Iβ1 subunit was expressed at all stages described above. However, we found a significant decrease of its mRNA level at day 3 with a small reduction of the protein expression. Altogether, these results show an active regulation of integrin gene expression during cardiac differentiation, particularly of those integrins involved in fibronectin signaling.
We then wondered if different hPSC lines share the same integrin expression profile that we observed in the NKX2-5 HES3 reporter cell line. To this end, we analyzed mRNA expression levels of two human-induced pluripotent cell lines (hiPS) and two human embryonic stem cell lines (hESC)(H1 and H9) by using previously generated RNA-seq data (Fig. S4)15. Interestingly, we found a similar profile of integrin expression in these samples, which remarks that integrin regulation during cardiac differentiation share the same behavior regardless of the pluripotent cell line.
To demonstrate that these results were not only a consequence of the monolayer differentiation system, we performed the same analysis during a 3D-cardiac differentiation protocol, which involves a whole different cell culture environment and possible ECM regulation (Fig. S5). Importantly, integrin expression was similar to that seen in the monolayer-cardiac protocol, suggesting that integrin regulation was indeed due to the cardiac differentiation process and not to the context of cell culture.
To further characterize the cell to ECM interaction during cardiac differentiation, we next studied the expression of integrin ligands during this protocol. We focused on fibronectin and laminin subunits since these proteins are the main ligands of the integrins subunits described above. We observed a significant up-regulation of fibronectin mRNA at day 3, consistent with its role in facilitating cell migration during EMT (Fig. 2). Laminin subunits also displayed a developmental stage-regulated gene expression distribution during cardiac differentiation (Fig. S6). The most remarkable subunits were laminin α2 and α4, which displayed a significant mRNA up-regulation in immature cardiomyocytes compared to undifferentiated hESCs (Fig. 2).
Upregulation of Iα5 subunit parallels CD56(+) cell population
Iα5 subunit is the main receptor for fibronectin and is highly expressed in many cell types. Moreover, it has been previously reported that knock-out mice for Iα5 die in utero due to cardiac defects10. Given the increase of the expression of Iα5 that we observed at day 3, we assessed the expression of CD56 on cell surface and studied deeper its relation with Iα5. At day 3, the protein expression of CD56 was significantly increased by 2-fold compared to this cell population on the previous day (day 2) (Fig. 3A). In coincidence to the up-regulation of CD56, the protein expression of Iα5 was also doubled during the same period. In summary, flow cytometry analysis revealed a parallel displacement of both cell surface markers during mesoderm differentiation raising the possibility that Iα5 might be involved in the early stages of mesoderm induction.
Silencing of Iα5 subunit impairs epithelial to mesenchymal transition
To investigate the role of this subunit in cardiac differentiation, we downregulated Iα5 subunit expression through CRISPRi system16,17. Briefly, this system works by expressing a doxycyclin (dox) inducible nuclease dead Cas9 fused to a transcriptional repressor (dCas9-KRAB). The simultaneous expression of a guide RNA directing the dCas9-KRAB to the promoter of a gene of interest leads to its transcriptional inactivation. We first generated a stable cell line expressing the dCas9-KRAB protein and confirmed its expression by immunofluorescence after 72 hours of dox-treatment (Fig. S7). The expression of dCas9-KRAB protein was not detected in cells not exposed to dox. Then, we designed a sgRNA sequence targeting 150 bp upstream the Iα5 subunit TSS and generated a clonal cell line, both for the constitutive expression of the sgRNA and the inducible expression of dCas9-KRAB. Silencing of Iα5 subunit was then evaluated at different time points post-dox treatment. We found a fast downregulation of the Iα5 subunit mRNA expression at 24 hours followed by a decrease of protein expression 24–48 hours later. This led to a down-regulation of Iα5 subunit protein expression in approximately 45% of cells after 48 hours, and a complete loss of expression after 96 hours of dox incubation in 85% of the cell population (Fig. 3B).
Iα5 subunit downregulation on HES3-hESC did not induce any evident phenotypic effect with no significant morphological changes in cell colonies in the short term. After 96 hours of dox incubation, we analyzed cell proliferation, apoptosis and mRNA gene expression of pluripotency transcription factors (Fig. S8). Cell cycle and apoptosis were evaluated by EdU incorporation and 7-AAD/Annexin staining, respectively. No significant differences were detected between the Iα5 silenced and the control cell line or the untreated condition in proliferation, apoptosis nor in mRNA levels of pluripotency transcription factors. Taken together, our results suggest that down-regulation of Iα5 subunit did not affect the pluripotent state of hESC.
Our previous results show that the highest mRNA and protein expression of Iα5 subunit was observed at the stage of mesodermal progenitor cells and in coincidence with the EMT process. Thus, we then investigated if the inhibition of Iα5 subunit during the first three days of cardiac differentiation would have an impact on mesoderm and cardiac induction. We first assessed the surface expression of CD56 at day 2 and day 3 as a marker of early MPC. We found that at day 2, cells in which Iα5 expression was downregulated displayed a significant increase in the MFI of CD56. However, we found no significant difference in CD56 expression at day 3 of cardiac differentiation (Fig. 3C).
We next analyzed the effect of Iα5 downregulation on the expression of several genes involved in mesoderm and cardiac specification. TBX6, an early mesoderm-related transcription factor, displayed a significant reduction in its mRNA levels after dox treatment. Coincident with this, TBX6 protein was highly expressed at day 4 in 78 ± 1% of the cells, whereas in dox-treated cells it was significantly reduced to 54 ± 1% (Fig. 4A). We also found that T/Brachyury gene expression was significantly down-regulated in dox-treated cells, but no significant differences where observed in the mesodermal transcription factors Eomes and Mesp1 (Fig. 4B). Furthermore, we evaluated whether there was a different mRNA expression of EMT markers in CD56(+) cells that were sorted according to Iα5 subunit expression at day 3. We found that the expression of Zeb-1 and Zeb-2 significantly increased in Iα5(+) cells compared to Iα5(−) cells while e-Cad significantly decreased (Fig. 4C). In summary, these results suggest a significant impairment in EMT and early mesoderm development after downregulation of Iα5 subunit. Even though the number of MPC (i.e., CD56+ cells) did not change, we found that the identity of this cell population was different as a consequence of a change in the expression of key genes.
Iα5 subunit expression and its possible regulation by mesoderm transcription factors in MPC
To investigate the presence of regulatory regions we analyzed the Iα5 subunit genomic locus in previous ChIP-Seq experiments during the generation of cardiomyocytes from several hPSC lines (Fig. S9)18. Mesendodermal cells were found to have a region close to the transcription start site (TSS) with H3K27 acetylation, a marker of an active enhancer, surrounded by mesendoderm transcription factors, including T/Brachyury, EOMES, SMAD3 and GATA4. All these transcription factors are involved in mesoderm development. Moreover, we found in the Iα5 subunit TSS itself a positive peak of phospho-RNAPol-II and H3K4Me bi/tri-methylated, pointing to an active transcription in this cell population. In hPSC however, Nanog and SOX2 are recruited close to this regulatory region without the H3K27 acetylation peak. In cardiac cells, the enhancer is again not active, and a small peak of transcription signals is evident at the TSS. Taken together, these results suggest that the increase of Iα5 subunit expression in MPC may be upregulated by the recruitment of key mesoderm transcription factors in a region neighboring the TSS.
Effects of Iα5 subunit downregulation on cardiac differentiation
Considering the qualitative effects of Iα5 subunit downregulation in MPC we then wondered if downregulation of Iα5 subunit during the first three days of differentiation would have an impact in mesoderm specification into cardiomyocytes. We analyzed mRNA expression of cardiac progenitors markers (GATA4, Islet-1 and NKX2-5) and a structural cardiomyocyte marker (cTnT) on both conditions at day 7 and day 15. GATA4 and ISL-1 were significantly reduced at day 7, while in immature cardiomyocytes (at day 15) NKX2-5 and cTnT were also reduced (Fig. 5B). At day 15, cellular network architecture was different, losing their typical structure with lower number of NKX2-5(+) cells compared to the control condition (Online Movies I–IV) (Fig. 5A). Flow cytometry analyses showed 22 ± 6% of NKX2-5(+) cells in dox+ compared to 60 ± 5% in dox− cells (Fig. 5C). Interestingly, approximately 10% of cardiomyocytes obtained in dox+ protocol still had a low integrin Iα5 subunit expression (Fig. S10).
A lower contractility of the cardiac cell population was evident under visual inspection in the Iα5-downregulated conditions. Thus, we quantitatively measured cardiomyocyte contractility at day 15 (Online Movies V and VI) (Fig. 5D). Importantly, contraction and peak amplitudes were significantly reduced in cardiomyocytes derived under Iα5 downregulated conditions. In summary, Iα5 subunit downregulation during the early stages of cardiac differentiation led to a reduction in cardiomyocyte differentiation and impaired contractility.
In the present work we analyzed mRNA and protein profiles of the most relevant integrins in different cell populations identified during the cardiac differentiation: human pluripotent stem cells, early mesodermal progenitor cells and cardiomyocytes. Our results revealed a pattern in the expression of integrin subunits at each stage of the cardiac specification. We found that one specific integrin subunit, Iα5, is highly expressed in early mesodermal progenitor cells. Interference of its expression at this stage led to changes in mesoderm progenitor cells that impaired normal cardiac differentiation.
The role of cell-substrate interaction in hPSC and in their specification to different lineages is not fully understood. Integrins have been recognized as key regulators in embryogenesis, though little is known in depth about how integrin signaling determines the cell fate19,20,21. Moreover, integrins play a key role in maintaining pluripotency itself. For example, Iα6 is a main integrin receptor in hPSC that prevents degradation of pluripotency transcription factors and maintains self-renewal22. We found a high expression of this integrin in hESC, with a significant downregulation upon differentiation. In the case of Iα5 subunit, it is widely expressed in many different cell types including hPSC, adult cardiomyocytes and other terminally differentiated cells like fibroblasts21. However, we found that Iα5 is significantly upregulated in MPC. We also found that its ligand, fibronectin, is also significantly upregulated at the same stage, as it was previously reported12,23. Of note, fibronectin has a key role in facilitating cell migration, and hence may be involved in mesoendoderm cell migration during embryonic EMT.
Iα5 subunit knockdown altered CD56(+) mesoderm progenitor cells developed during cardiac differentiation with the expression of EMT markers such as Zeb-1 and Zeb-2 being impaired in these cells. In addition, mesendoderm markers such as T/Brachyury and TBX6 were significantly reduced. Hence, we demonstrated that the repression of this integrin impaired EMT and the efficient differentiation to the mesoderm linage. Importantly, previous works showed that knockdown of Iα5 subunit led to mesodermal defects in mice embryogenesis10,11. It has been previously reported that activation of Iα5β1 modulates BMP4 expression, which is essential for initiating mesoderm induction24. Thus, we confirm in human cells previous findings in the mouse suggesting a role of Iα5 in mesoderm and cardiac differentiation. It would thus be interesting to ascertain the connection of the BMP4 pathway with the effects of Iα5 downregulation during cardiac differentiation of hPSCs.
Our ChIP-seq data analysis might shed light on the mechanism by which Iα5 subunit is upregulated in MPC. As we showed, there is a regulatory region where mesoderm transcription factors as T/Brachyury and EOMES are recruited to enhance Iα5 subunit expression. It has been previously reported that EMT positively regulates Iα5 expression25, but there is no information about its regulation by mesoderm transcription factors. Further experiments must be done in order to find out whether this region is actually functional.
Importantly, we showed that Iα5 subunit knockdown led to a reduction in the efficiency of cardiac differentiation. We also found that those cardiomyocytes that were able to differentiate had an impaired contractility. Interestingly, it has been previously reported that fibronectin increased cardiac contractility by signaling through Iα5 and increasing intracellular Ca++ concentrations26.
In summary, our results showed a link between changes in cell identity and the regulation of integrin expression during cardiac differentiation. We showed that Iα5 subunit is relevant in this process. Thus, our results further confirm that cell-substrate interactions through integrins are key points for successful cardiac specification during embryonic differentiation.
Maintenance of hPSCs
Human embryonic stem cells (HES3 NKX2-5eGFP/w, passage 40 + 10) were generously donated by Edouard Stanley’s Lab14. hPSCs were maintained with normal karyotype in a feeder-free conditions on Geltrex™ coated plates (diluted 1:1000 from 15 mg/ml; Thermo Fisher Scientific) in mTeSR1 medium (StemCell Technologies). This cell line has been genetically modified at the Monash Immunology and Stem Cell Laboratory to express e-GFP under the promoter of NKX2-5. All cell cultures were maintained at 37 °C in a humidified atmosphere with 5% CO2.
Monolayer Cardiac Differentiation
hPSCs maintained on Geltrex in mTeSR1 were dissociated into single cells with TrypLE TM Select (1X; Thermo Fisher Scientific) at 37 °C for 5 minutes and then seeded onto a Geltrex-coated cell-culture dish at 150,000 cell/cm2 in mTeSR1 supplemented with 5 μM ROCK inhibitor (Y-27632) (day-3) for 24 hours. When high confluence was achieved, cells were incubated with 12 μM CHIR99021 (Tocris) in RPMI/B27 (no insulin) medium for 24 hours (day 0 to day 1). At day 3, 5 μM IWP2 (Tocris) was added to the medium and removed at day 5. Cells were then grown in the RPMI/B27; medium was changed every 3 days. At day 15 the percentage of NKX2-5/GFP(+) cells were analyzed by Flow Cytometry. At this stage, cardiomyocytes are differentiated up to the point of showing spontaneous beating activity27.
3D Cardiac Differentiation
In order to generate cardiac embryoid bodies (cEBs), hPSCs were incubated with 1 mg/mL of collagenase I (Sigma-Aldrich) in PBS with Ca++ and Mg++ supplemented with 20% FBS for 20 minutes at 37 °C. Afterwards, cells were detached to form small aggregates of 10 to 20 cells by 0.05% Trypsin-EDTA (Thermo Fisher Scientific) digestion and mechanical scrapping. Aggregates were plated in ultra-low attachment plates (Corning) at 37 °C and 5% CO22with the following basal culture medium: StemPro®-34 SFM (Life Technologies), 1% glutamine, 1% penicillin–streptomycin, 150 μg/mL transferrin (Roche Life Sciences), 0.039 μL/mL monothioglycerol (Sigma-Aldrich), 50 μg/mL ascorbic acid (Sigma-Aldrich). To induce differentiation, the basal culture medium was supplemented with BMP4 (Tocris), bFGF (Thermo Fisher Scientific), Activin A (Tocris), and the Wnt/B-catenin inhibitor XAV939 (Tocris). At day 15 the percentage of NKX2-5/GFP(+) cells were analyzed by flow cytometry. Again, these cardiomyocytes shows spontaneous beating activity28.
gRNA Design and Cloning into the gRNA-Expression Vector
Two sgRNAs were designed to target close to the TSS of the gene of interest (250 bp upstream and downstream) using the CRISPR Design Tool. sgRNA oligos were designed, phosphorylated, annealed, and cloned into the pLenti-Sp-BsmBI-sgRNA-Puro vector (Addgene plasmid number 62207) using BsmBI ligation strategy (Promega). The list of sgRNA sequences are listed in supplemental experimental procedures (Table S1)16,17.
Lentiviral particles production
Lentivirus were produced in HEK293FT cell line (Thermo Fisher Scientific). Briefly, pHAGE TRE–dCas9–KRAB (Addgene 50917) and the sgRNA coding plasmid (Addgene 62207) were transfected with 3rd generation lentiviral packaging plasmids using X-tremeGENE 9 DNA transfection reagent (Roche) according to the manufacturer’s instructions. Virus was harvested 48 h after transfection.
Generation of stable HES3 NKX2-5eGFP/w TRE–dCas9–KRAB cell line
HES3 NKX2-5eGFP/w were dissociated to single cells with TrypLE TM Select (1X; Thermo Fisher Scientific) and then were seeded at low confluence onto a Geltrex-coated cell-culture 6-well plates. At 24 h, they were incubated overnight with TRE–dCas9–KRAB lentivirus. 48 h after transduction, cells were treated with G418 100 μg/ml (Gibco, 10131). Following 4 days of selection, a limiting dilution of the resulting pool of G418-resistant cells was done. Finally, cells were grown in mTeSR supplemented with Y-27632 (10 mM) for 7–10 days until robust individual clonal lines were obtained. The same protocol was performed when KRAB stable cell line was transduced with Iα5-sgRNA lentivirus. Cells were treated with 250 ng/ml dox (Sigma-Aldrich) to induce expression of dCas9-KRAB.
Quantitative analysis of cardiac contraction
The software tool Muscle Motion was used to measure cardiac contraction29. Movies (60 fps) of several areas of the cardiomyocyte monolayer were recorded in control and dox-treated cells by using a high-speed recording camera steadily mounted on the microscope.
DNA replication analysis
Analysis of DNA replication by EdU incorporation was performed using the Click-iT EdU Flow Cytometry Kit (Thermo Fisher Scientific), following manufacturer’s instructions. Cells were pulsed with EdU at a final concentration of 10 μM for 30 minutes at 37 °C.
cEBs and 2D cardiac cultures were dissociated by incubation with TrypLE (Thermo Fisher Scientific) and then cells were stained for the presence of specific markers. For cell surface markers, staining was carried out in 1X PBS with 0.5% BSA. For intracellular proteins, staining was carried out on cells fixed with 4% paraformaldehyde in PBS. The staining was done in PBS with 0.5% BSA and 0.5% Saponin (Sigma). Apoptosis measurements were performed using the Annexin V-PE and Propidium Iodide (PI) kit (BD Pharmigen) following manufacturer’s instructions. For Annexin V/PI double staining, samples were stained at room temperature with Annexin V and IP for 15 minutes in the dark. Flow cytometry analyses were performed in a BD Accuri cytometer. Data were analyzed with FlowJo software. Primary antibodies are listed in supplemental experimental procedures (Table S2).
Quantitative Real-Time PCR
Total RNA was extracted with Trizol (Thermo Fisher Scientific) following manufacturer’s instructions and reverse transcribed using M-MLV Reverse Transcriptase (Promega). Quantitative PCR was performed using a StepOnePlus Real Time PCR System (Applied Biosystems). Primers efficiency and N0 values were determined by LinReg software30, and gene expression was normalized to RPL7 housekeeping genes N0, for each condition. Sequences for all primers used in RT-qPCR analysis are listed in the Supplemental Tables section (Table S3). All experiments were performed in at least three biological replicates, with two technical replicates for each condition.
Experimental results are presented as mean ± standard error of the mean (SEM) of at least three biological replicates. Statistical significance between groups was analyzed using randomized block design (RBD) ANOVA. Residuals fitted normal distribution and homogeneity of variance. Comparisons between means were assessed using the Tukey test. Statistical analysis was performed using Infostat Software.
Bergmann, O. et al. Evidence for cardiomyocyte renewal in humans. Science 324, 98–102 (2017).
Burridge, P. W., Keller, G., Gold, J. D. & Wu, J. C. Production of de novo cardiomyocytes: Human pluripotent stem cell differentiation and direct reprogramming. Cell Stem Cell 10, 16–28 (2012).
Watt, F. M. & Huck, W. T. S. Role of the extracellular matrix in regulating stem cell fate. Nature Reviews Molecular Cell Biology 14, 467–473 (2013).
Chan, C. K. et al. Differentiation of cardiomyocytes from human embryonic stem cells is accompanied by changes in the extracellular matrix production of versican and hyaluronan. Journal of cellular biochemistry 111, 585–96 (2010).
Votteler, M., Kluger, P. J., Walles, H. & Schenke-Layland, K. Stem Cell Microenvironments - Unveiling the Secret of How Stem Cell Fate is Defined. Macromolecular Bioscience 10, 1302–1315 (2010).
Takada, Y., Ye, X. & Simon, S. The integrins. Genome Biology 8 (2007).
Barczyk, M., Carracedo, S. & Gullberg, D. Integrins. Cell and Tissue Research 339, 269–280 (2010).
Israeli-Rosenberg, S., Manso, A. M., Okada, H. & Ross, R. S. Integrins and integrin-associated proteins in the cardiac myocyte. Circulation Research 114, 572–586 (2014).
Brancaccio, M. et al. Differential Onset of Expression of α7 and β1D Integrins During Mouse Heart and Skeletal Muscle Development. Cell Adhesion and Communication 5, 193–205 (1998).
Yang, J. T., Rayburn, H. & Hynes, R. O. Embryonic mesodermal defects in alpha 5 integrin-deficient mice. Development (Cambridge, England) 119, 1093–1105 (1993).
Sierra, H., Cordova, M., Chen, C. S. J. & Rajadhyaksha, M. Confocal imaging-guided laser ablation of basal cell carcinomas: An ex vivo study. Journal of Investigative Dermatology 135, 612–615 (2015).
Evseenko, D. et al. Mapping the first stages of mesoderm commitment during differentiation of human embryonic stem cells. Proc Natl Acad Sci USA 107, 13742–7 (2010).
Garate, X. et al. Identification of the mirnaome of early mesoderm progenitor cells and cardiomyocytes derived from human pluripotent stem cells. Sci Rep 8, 8072 (2018).
Elliott, D. A. et al. Nkx2-5(egfp/w) hescs for isolation of human cardiac progenitors and cardiomyocytes. Nat Methods 8, 1037–40 (2011).
Liu, Q. et al. Genome-wide temporal profiling of transcriptome and open chromatin of early cardiomyocyte differentiation derived from hipscs and hescs. Circ Res 121, 376–391 (2017).
Kearns, N. A. et al. Cas9 effector-mediated regulation of transcription and differentiation in human pluripotent stem cells. Development 141, 219–223 (2014).
Walker, J. M. Eukaryotic Transcriptional and Post-Transcriptional Gene Expression Regulation. Springer Protocols 1507, 1–265 (2017).
Oki, S. et al. Chip-atlas: a data-mining suite powered by full integration of public chip-seq data. EMBO Rep 19 (2018).
Vitillo, L. & Kimber, S. J. Integrin and FAK Regulation of Human Pluripotent Stem Cells. Current Stem Cell Reports 358–365 (2017).
Darribére, T. et al. Integrins: Regulators of embryogenesis. Biology of the Cell 92, 5–25 (2000).
Wang, H., Luo, X. & Leighton, J. Extracellular Matrix and Integrins in Embryonic Stem Cell Differentiation Supplementary Issue: Biochemistry of the Individual Living Cell. Biochemistry insights 8 (2015).
Villa-Diaz, L. G., Kim, J. K., Laperle, A., Palecek, S. P. & Krebsbach, P. H. Inhibition of Focal Adhesion Kinase Signaling by Integrin α6β1 Supports Human Pluripotent Stem Cell Self-Renewal. Stem Cells 34, 1753–1764 (2016).
Hay, E. D. An overview of epithelio-mesenchymal transformation. Acta Anat (Basel) 154, 8–20 (1995).
Tan, T. W. et al. CCN3 increases BMP-4 expression and bone mineralization in osteoblasts. Journal of Cellular Physiology 227, 2531–2541 (2012).
Nam, E.-H., Lee, Y., Park, Y.-K., Lee, J. W. & Kim, S. Zeb2 upregulates integrin α5 expression through cooperation with sp1 to induce invasion during epithelial-mesenchymal transition of human cancer cells. Carcinogenesis 33, 563–71 (2012).
Wu, X. et al. Fibronectin increases the force production of mouse papillary muscles via α5β1 integrin. J Mol Cell Cardiol 50, 203–13 (2011).
Lian, X. et al. Robust cardiomyocyte differentiation from human pluripotent stem cells via temporal modulation of canonical Wnt signaling. PNAS 109, 1848–57 (2012).
Kattman, S. J. et al. Stage-specific optimization of activin/nodal and BMP signaling promotes cardiac differentiation of mouse and human pluripotent stem cell lines. Cell Stem Cell 8, 228–240 (2011).
Sala, L. et al. Musclemotion: A versatile open software tool to quantify cardiomyocyte and cardiac muscle contraction in vitro and in vivo. Circ Res 122, e5–e16 (2018).
Ruijter, J. M. et al. Amplification efficiency: Linking baseline and bias in the analysis of quantitative PCR data. Nucleic Acids Research 37, e45 (2009).
We thanks Fundación FLENI and Fundación Pérez Companc for their continuing support. The following grants proivided financial support to this work: FONCYT: PICT-2011-1927, PICT-2015-1469, and PID-2014-0052; CONICET: PIP2015-2017.
The authors declare no competing interests.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Neiman, G., Scarafía, M.A., La Greca, A. et al. Integrin alpha-5 subunit is critical for the early stages of human pluripotent stem cell cardiac differentiation. Sci Rep 9, 18077 (2019). https://doi.org/10.1038/s41598-019-54352-2
This article is cited by
Gene Modulation with CRISPR-based Tools in Human iPSC-Cardiomyocytes
Stem Cell Reviews and Reports (2023)
Downregulation of E-cadherin in pluripotent stem cells triggers partial EMT
Scientific Reports (2021)
Cell surface markers for immunophenotyping human pluripotent stem cell-derived cardiomyocytes
Pflügers Archiv - European Journal of Physiology (2021)
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.