Factors Expressed by Murine Embryonic Pancreatic Mesenchyme Enhance Generation of Insulin-Producing Cells From hESCs
- Diabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, California
- Corresponding author: Matthias Hebrok, .
Islet transplantation has proven to be a successful strategy to restore normoglycemia in patients with type 1 diabetes (T1D). However, the dearth of cadaveric islets available for transplantation hampers the widespread application of this treatment option. Although human embryonic stem cells and induced pluripotent stem cells are capable of generating insulin-producing cells in vitro when provided with the appropriate inductive cues, the insulin-expressing cells that develop behave more like immature β-cells with minimal sensitivity to glucose stimulation. Here, we identify a set of signaling factors expressed in mouse embryonic mesenchyme during the time when foregut and pancreatic progenitors are specified and test their activities during in vitro differentiation of human embryonic stem cells. Several of the identified factors work in concert to expand the pancreatic progenitor pool. Interestingly, transforming growth factor (TGF)-β ligands, most potent in inducing pancreatic progenitors, display strong inhibitory effects on subsequent endocrine cell differentiation. Treatment with TGF-β ligands, followed by the addition of a TGF-β receptor antagonist, dramatically increased the number of insulin-producing cells in vitro, demonstrating the need for dynamic temporal regulation of TGF-β signaling during in vitro differentiation. These studies illustrate the need to precisely mimic the in vivo conditions to fully recapitulate pancreatic lineage specification in vitro.
Islet transplantation has opened up the possibility to treat diabetic patients with cell replacement strategies (1–3). Because the demand for pancreatic islet cells far outstrips the supply, concerted efforts have been undertaken to generate a renewable and reliable supply of insulin-producing cells from human embryonic stem cells (hESCs) and induced pluripotent stem cells. Recently, strategies have been devised that aim to recapitulate the stepwise succession of signals that guide the development of pancreatic endocrine and β-cells during embryogenesis. Recapitulation of these embryonic signals in cell culture has led to the production of intermediate pancreatic lineage as well as immature, nonfunctional insulin-producing cells from hESCs and induced pluripotent stem cells in vitro (4–9). More importantly, when transplanted in vivo, pancreatic progenitor cells generated from hESCs gave rise to mature β-cells capable of reverting diabetic phenotypes caused by chemically induced depletion of endogenous β-cells in mice (10). Although these proof-of-principle experiments clearly demonstrated that pancreatic cells generated in vitro were capable of carrying physiological functions in vivo, they also illustrated that critical signals promoting the full differentiation of pancreas endocrine progenitors and mature endocrine cells were missing from the current in vitro conditions.
The pancreas arises from the definitive endoderm, one of the three primary germ layers generated through gastrulation during early embryogenesis (11). Multiple organs, including the notochord and the dorsal aorta, secrete signaling molecules that control the specification of the duodenal part of the posterior foregut from which the pancreatic bud emerges (12–15). At approximately embryonic day 9.5 (E9.5), a layer of mesenchyme condenses around the budding pancreatic epithelium and separates it from the adjacent notochord and dorsal aorta (16,17). Studies initiated by Golosow and Grobstein (18) in the 1960s posed that the pancreatic mesenchyme provides factors necessary for the survival and cytodifferentiation of the developing pancreatic epithelium. Because clean separation of the mesenchyme from the branching pancreas epithelium is difficult at later stages, a full account of all mesenchymal factors expressed throughout pancreas development and how they function individually or in combination is currently missing.
Here, we provide evidence that embryonic pancreas mesenchyme provides temporally distinct signals that promote specific stages of hESC differentiation toward pancreatic progenitors and insulin-producing cells. Microarray analysis of RNAs collected from E11.5 mouse pancreatic mesenchyme and epithelium allowed us to select 11 genes encoding for secreted factors that are preferentially expressed at higher levels in the mesenchyme compared with the pancreatic epithelium. Applying these candidate factors individually and combined with an established in vitro hESC differentiation system revealed that they greatly improved the generation of pancreatic progenitors. In contrast, sustained treatment with these factors beyond the progenitor stage blocked further differentiation into endocrine progenitor and insulin-producing cells. Summarily, our studies illustrate that tight temporal recapitulation of embryonic signaling events is critical for the optimization of hESC-derived pancreatic endocrine cells.
RESEARCH DESIGN AND METHODS
The mice used in this study were maintained according to protocols approved by the University of California, San Francisco Committee on Animal Research. CD1 mice were obtained from Charles River Laboratories. Noon on the day a vaginal plug was detected was considered as E0.5. Whole embryos were fixed using the HEPES glutamic acid buffer–mediated organic solvent protection effect (HOPE; DCS Innovative Diagnostik-systeme, Germany) according to the manufacturer’s protocol. Embryos were embedded in paraffin overnight before being cut into 5-μm sections and mounted onto 2-μm polyethylene naphthalate–membrane slides (Leica).
Laser capture microdissection.
Slides were stained with hematoxylin (Sigma-Aldrich), followed by staining with eosin (Protocol). Slides were then microdissected using the Leica Laser Micro Dissection Microscope LMD 2000 (Leica).
RNA was processed by the Gladstone Genome Core. RNAs collected from laser capture microdissection (LCM) was extracted using the PicoPure RNA isolation kit (Arturus) and further amplified using the NuGEN WT-Ovation Pico RNA Amplification kit (NuGEN), following the manufacturer’s instruction. Gene array was performed using Mouse Gene 1.0 ST arrays, following the manufacturer’s instruction (Affymetrix).
Undifferentiated Cythera 49 and MEL 1 INS GFP/w cells (19) were maintained on mouse embryo fibroblast feeder layers (Millipore). Standard differentiation was carried out as described previously (4,10).
Test of mesenchymal factors.
Growth factors (R&D Systems) were used at the following concentrations: angiotensin-1, 20 ng/mL; CXC chemokine ligand-13, 5 ng/mL; fibroblast growth factor-9 (FGF-9), 4 ng/mL; hepatocyte growth factor, 50 ng/mL; IGF, 50 ng/mL; platelet-derived growth factor, 10 ng/mL; transforming growth factor (TGF)-β2, 2 ng/mL; TGF-β3, 5 ng/mL; and vascular endothelial growth factor (VEGF), 100 ng/mL. For the TGF-β2/3 combination, 1 ng/mL TGF-β2 was mixed with 2 ng/mL TGF-β3.
Cells were fixed using an adapted protocol published previously (4). Antibodies used are listed in Supplementary Table 2. Images were taken with Olympus IX70 fluorescence microscope (Olympus), ApoTome.2 widefield microscope (Carl Zeiss, Inc), or InCell Analyzer 2000 for quantification (GE Healthcare).
Ten fields from each well were picked at random for quantification analysis. The pancreatic duodenal homeobox-1 (PDX1)-positive area was calculated in relation to the area occupied by DAPI-positive nuclei. For the proliferation index, phospho-Histone-H3–positive cells were normalized to the total number of PDX1- or DAPI-positive cells. The percentage of insulin-positive cells was calculated by dividing the number of insulin-expressing cells by the total cell number.
Real-time quantitative PCR.
RNA extraction was performed using RNeasy micro kit, as instructed by the manufacturer (Qiagen), then reverse-transcribed with the iScript cDNA synthesis kit (Bio-Rad). Human islet cDNA was obtained from The Hebrew University of Jerusalem. Real-time PCR was performed on the 7900 HT Fast Real-Time PCR System (Applied Biosystems) using a protocol described previously (4). Primer sequences are listed in Supplementary Table 3.
C-peptide content and release assays.
C-peptide levels in culture supernatants or cell lysates were measured using ultrasensitive C-peptide ELISA (Mercodia AB). For total C-peptide content analysis, day 15 cell cultures were scraped and sonicated in 300 μL water. DNA content was measured using PicoGreen (Invitrogen). C-peptide release was measured by a protocol described previously (4).
P values were determined using the unpaired, two-tailed Student t test. Error bars in the bar diagrams represent the standard deviation of the samples.
Identification of candidate factors from mouse embryonic pancreas mesenchyme.
To identify soluble factors secreted by the pancreatic mesenchyme, we separated pancreatic epithelium and mesenchyme from wild-type mouse embryos at E11.5 via LCM (Fig. 1A and B and Supplementary Fig. 1). Differential gene expression arrays were performed to compare cDNA samples collected from pancreatic endoderm and pancreatic mesenchyme. To determine potential tissue specific factors unique to pancreas mesenchyme, we included cDNAs from stomach and intestinal mesenchyme as well. Microarray analysis revealed that pancreatic mesenchyme has a distinct gene expression pattern compared with pancreatic endoderm (Fig. 1C). In contrast, the transcriptional signature for all of the mesenchymal tissues analyzed was remarkably similar (Fig. 1C). From this dataset, we identified 11 secreted factors that belong to several signaling pathways, including the TGF-β, FGF, and Wnt pathways, and are preferentially expressed in the mesenchymal compared with the pancreatic endoderm for further analysis (Fig. 1D).
Combinations of mesenchymal factors elicit different effects on distinct hESC populations.
Considering that all factors are expressed concomitantly during embryogenesis, we first investigated their combined effects during hESC to β-cell differentiation using the protocol originally described by Kroon and colleagues (4,9,10). Under the conditions used for the original protocol (referred to as the standard protocol hereafter), hESCs progress through distinct stages (Fig. 2A). To mimic the interaction between pancreatic epithelium and pancreatic mesenchyme at ∼E11.5, the time point of gene array analysis, we tested the effects of the combined mesenchymal factors on primitive gut tube cells generated via the standard protocol (factors were added after day 6 of the standard protocol) (10). At that time, control samples received standard factors retinoic acid, sonic hedgehog inhibitor (3-Keto-N-[aminoethyl-aminocaproyl-dihydrocinnamoyl]-cyclopamine), and the bone morphogenetic protein antagonist Noggin (referred to as R/K/N hereafter) between days 7 and 9, while experimental samples were treated with R/K/N plus the 11 mesenchymal factors. Starting at day 7, cells aggregated into clusters under control and experimental conditions (Supplementary Fig. 2). Immunostaining for PDX1 and hepatic nuclear factor 6 (HNF6), two key pancreatic/foregut progenitor markers, were used to monitor the generation of pancreatic lineage at day 9 (21–23). Samples treated with mesenchymal factor displayed more PDX1-positive cells, and cultures expressed higher levels of PDX1 transcript than the control (Fig. 2B and C).
To test the effects of mesenchymal factors on the continued differentiation of PDX1-positive cells into hormone-expressing cells, combined factors (CF) were added between days 10 and 12, immediately after the induction of PDX1. On day 15, samples were stained with insulin, glucagon, or PDX1 to identify the extent to which pancreatic endocrine cells had formed. In control samples, insulin- and glucagon-expressing cells were seen throughout the culture. Samples treated with CF between days 10 and 12 displayed a considerably lower number of hormone-expressing cells compared with the control samples (Fig. 2D). Also, despite significant increases in PDX1 expression at early stages, samples treated with mesenchymal factors between days 7 and 9 were almost completely devoid of insulin- or glucagon-positive cells (Fig. 2D). Quantitative (Q)-PCR analysis confirmed the dramatic inhibition of insulin (INS) expression in CF-treated samples (both between days 7 and 9 and days 10 and 12), with the most severe inhibition observed when cells were treated from day 7 to 9 (Fig. 2E). At day 15, a large population of PDX1-positive, insulin-negative cells was found in samples treated with CF from day 7 to 9 (data not shown). No excess amount of exocrine markers was detected by Q-PCR in the CF-treated samples (Supplementary Fig. 3). These results suggest that candidate factors identified from E11.5 pancreas mesenchyme promote the induction of the pancreatic and foregut progenitors but prohibit the further differentiation and maturation of endocrine cells. Furthermore, the effects of the mesenchymal factors seem to be stage-specific, with the most robust phenotypes observed when cells are treated from day 7 to 9.
Effects of individual mesenchymal factors on pancreatic progenitor determination.
Because the combined factors dramatically enhanced the induction of pancreatic/foregut progenitors, we decided to test the activities of individual factors on the induction of PDX1-positive cells. Previous results with CF condition indicated that the most effective window for promoting pancreatic progenitors was between days 7 and 9. When single mesenchymal factors were applied alone (without R/K/N) from day 7 to 9, few PDX1-positive cells were detected on day 9 (Supplementary Fig. 4). This suggests that the mesenchymal factors tested individually do not effectively induce the formation of pancreatic progenitors. Considering that in the standard protocol R/K/N treatment is sufficient to induce PDX1 expression (4,10), we examined whether introducing single mesenchymal factors in combination with R/K/N could further promote PDX1 expression. Immunostaining performed at day 9 detected an increase in PDX1-positive cells in samples treated with R/K/N plus certain mesenchymal factors compared with R/K/N alone (Fig. 3A and D). Of note, treatment with individual factors did not dramatically affect the proliferative capacity of the entire cellular pool or the PDX1-positive cells (Fig. 3B and C). Thus, our results indicate that mesenchymal factors identified from the embryonic pancreas mesenchyme promote the formation of pancreatic progenitors in conjunction with R/K/N, likely through direct conversion of primitive gut cells into PDX1-expressing pancreatic progenitors instead of the expansion of existing PDX1-positive cells.
TGF-β signaling improves PDX1 expression but inhibits endocrine cell differentiation.
Among the 11 tested factors, TGF-β2 and TGF-β3 were more potent than the other mesenchymal factors, showing a 3.2- and 4.6-fold increase in PDX1-positive cells compared with the controls, respectively (Fig. 3A and D). TGF-β signaling is known to regulate multiple cell functions, including proliferation and differentiation in adult tissue and also during embryogenesis (24). When added together between days 7 and 9 in addition to R/K/N, TGF-β2 and 3 (referred to as TGF-β2/3 hereafter) induced a significant increase in PDX1-positive cells over the standard condition (analysis at day 9; Fig. 4A and B). Q-PCR analysis also revealed a significant increase in PDX1 gene expression on day 9 and day 15 in TGF-β2/3–treated samples (Fig. 4C and D). However, as observed under conditions when all factors are combined, TGF-β2/3 treatment from day 7 to 9 dramatically decreased INS expression levels and the number of insulin-positive cells on day 15 (Fig. 4E and F). At this point, most of the cells in TGF-β2/3– treated samples remain PDX1-positive but insulin-negative (Fig. 4F insets), suggesting the existence of a large population of pancreatic progenitors. Therefore, TGF-β signaling enhances the induction of pancreatic progenitors but subsequently blocks endocrine cell differentiation.
Precise activation of TGF-β signaling improves endocrine cell maturation.
Because activation of the TGF-β pathway from day 7 to 9 resulted in a severe reduction of endocrine lineages, we next tried to regulate TGF-β signaling in a more precise manner by performing time course experiments between days 7 and 9. Q-PCR results on day 15 samples showed that addition of TGF-β2/3 for only 1 day (day 7), increased INS expression by twofold (Fig. 5A); 2-day TGF-β2/3 treatment (day 7–8) showed slightly lower but not significantly different INS expression levels, whereas applying TGF-β2/3 for 3 days (day 7 to 9) significantly decreased INS level compared with control. On the basis of these results, we decided to focus on a short, 1-day only (day 7) activation of TGF-β signaling for subsequent experiments. Cells were treated with R/K/N plus TGF-β2/3 for 24 h on day 7 and then continued to differentiate for 2 more days with R/K/N. On day 9, samples were stained for PDX1 and HNF6. TGF-β2/3–treated samples displayed more PDX1 and HNF6 double-positive cells (Fig. 5B), indicating efficient induction of pancreatic/foregut progenitors. Q-PCR also confirmed that 1-day TGF-β2/3 treatment enhanced PDX1 expression compared with control cells (Supplementary Fig. 5).
Proliferation and differentiation are two tightly regulated events during normal pancreas development. After expansion, pancreatic progenitors reduce proliferation rates and transiently turn on the endocrine master regulator neurogenin-3 (NGN3) (25,26). After 1 day of TGF-β2/3 treatment, we detected dramatically higher levels of NGN3 compared with the control cells (Fig. 5C). However, prolonged treatment with TGF-β2/3 for 3 days resulted in significantly lower NGN3 expression on day 9 (Fig. 5C). These results indicate that transient activation of TGF-β signaling facilitates pancreatic progenitor differentiation toward endocrine precursors at day 9 of in vitro differentiation. The increased expression of NGN3 in TGF-β2/3–treated samples resulted in a greater number of endocrine cells, including single- and double-hormone–positive cells compared with the samples treated with the standard protocol (Fig. 5D).
Inhibition of TGF-β signaling after progenitor induction further potentiates the differentiation of endocrine cells.
Taken together, our data demonstrate that prolonged activation of the TGF-β pathway prevented the generation of endocrine precursors. We then decided to test whether inhibiting TGF-β signaling by applying a TGF-β receptor (activin-like kinase 5) antagonist, 2-(3-(6-Methylpyridin-2-yl)-1H-pyrazol-4-yl)-1,5-naphthyridine (ALK5 inhibitor II) would promote the development of the endocrine lineage (27). Addition of the ALK5 inhibitor from day 7 to 9 led to decreased total cell numbers as well as the number of PDX1-positive cells on day 9 (data not shown). When the ALK5 inhibitor was added from day 10 onwards, significantly higher levels of NGN3 were observed on day 12 by Q-PCR, indicating the progression of pancreatic progenitor cells into endocrine precursors (Fig. 6A). To test whether addition of the ALK5 inhibitor could reverse the adverse effects of prolonged TGF-β activation at earlier time points, we performed time course experiments with TGF-β2/3 treatment at day 7, day 7–8, or day 7–9, followed by inhibition of this pathway via application of the ALK5 inhibitor from day 10 to 15. Similar to the earlier time course experiments (Fig. 5A), treatment with the ALK5 inhibitor after transient activation of TGF-β signaling on day 7 gave the most robust increase in INS expression over the standard protocol (Fig. 6B). In contrast, prolonged TGF-β activation resulted in smaller augmentation in INS expression (Fig. 6B).
To confirm that TGF-β activation is necessary before inhibition of the pathway, we differentiated hESCs according to the standard protocol until day 9 and then applied the ALK5 inhibitor to block the TGF-β pathway from day 10 to 12. Confirming prior studies (27–29), we observed higher numbers of insulin- and glucagon-positive cells as well as elevated INS expression level under these conditions compared with the standard condition (Fig. 6C–E). However, short activation of TGF-β2/3 at day 7, followed by ALK5 inhibition from day 10 to 15, resulted in the most significant increase in the number of endocrine cells. Detailed quantitative analysis revealed that the modified protocol typically generated 2.3 million cells at day 15 from a starting population of 1 million undifferentiated cells, among which an average of 8.5% and as many as 15% are insulin-expressing cells (Fig. 6C and D and Supplemental Fig. 6). Q-PCR analysis revealed an almost threefold increase in INS gene expression in TGF-β2/3–ALK5 inhibitor samples over those treated with the standard protocol plus ALK5 inhibitor alone (Fig. 6E). Samples receiving TGF-β2/3 and ALK5 inhibitor also showed a significantly higher level of PDX1 expression compared with control samples and samples treated only with the ALK5 inhibitor (Fig. 6F). Similar results were obtained when the modified protocol was tested on MEL1 INSGFP/w hESCs (19), with an average of 8.7% cells being insulin-positive on day 15 (Supplementary Fig. 7). Thus, our data demonstrate that finely tuned activation of TGF-β signaling, followed by pathway inhibition, increases formation of pancreas progenitors and insulin-producing endocrine cells.
Characterization of hESC-derived insulin-producing cells.
To further characterize the insulin-producing cells generated in vitro with our modified differentiation protocol (TGF-β2/3 on day 7, followed by ALK5 inhibition between day 10 and 15), we performed immunostaining with multiple markers. Approximately 40% of insulin-expressing cells were insulin-, glucagon double-positive cells, as previously reported (4) and likely resemble immature β-cells (Fig. 7A and data not shown). Most of the insulin-positive cells were double-labeled with C-peptide, indicating that these cells can properly process proinsulin (Fig. 7B). We also observed a small percentage of somatostatin-positive cells, with or without insulin staining (Fig. 7C). More important, most of the insulin-positive cells expressed PDX1 at high levels compared with the insulin-negative, PDX1-positive cells, likely representing pancreatic/foregut progenitors (Fig. 7D, arrows vs. arrowheads). Immunostaining with two essential NK homeodomain factors found in islet β-cells, NKX2.2 and NKX6.1 (30,31), revealed that a subset of insulin-expressing cells were positive for these markers (Fig. 7E and F). These staining results indicate that the insulin-producing cells generated in vitro possess many but not all characteristics of “authentic” pancreatic β-cells. When compared with adult human islets using Q-PCR, hESC-derived tissue showed lower expression of INS and NKX6.1 but a comparable level of PDX1 (Fig. 7G).
We furthermore examined the C-peptide content in the insulin-expressing cells. After 15 days of differentiation, the insulin-producing cells generated under modified conditions had significantly higher C-peptide content compared with control cells (Fig. 7H).
To further examine the physiological function of the insulin-expressing cells generated in vitro, we monitored C-peptide release upon stimulation. Insulin-producing cells from the control and modified protocols can both be directly depolarized by chemicals, such as potassium chloride (KCL), which promote insulin secretion without glucose stimulation, and showed a fourfold increase in C-peptide release compared with basal conditions (Fig. 7I). In contrast, in only one of five times did we detect slight C-peptide induction upon d-glucose stimulation over basal condition in samples treated with the modified protocol (Fig. 7I). Our results therefore suggest that the insulin-producing cells generated in vitro may have immature glucose-sensing and -transporting machinery compared with the bona fide pancreatic β-cells. This agrees with the recent finding that hESC-generated insulin-producing cells have less efficient Ca2+ influx upon glucose stimulation (32).
Finally we examined whether hESC-derived pancreatic endoderm can further mature in vivo. Four months after transplantation, pancreatic progenitors generated with TGF-β2/3 treatment on D7 matured to single hormone-positive, insulin-expressing cells with high levels of PDX1 and NKX6.1, as well as CK19-positive ductal cells and rare amylase-positive acinar cells (Supplementary Fig. 8), indicating their full differentiation potential toward pancreatic lineages.
Seminal work performed in the 1960s demonstrated crucial roles for the pancreatic mesenchyme in regulating epithelial cell development and differentiation (18,33). Although the filter pores used in the classical mesenchyme and epithelial coculture studies were large enough to allow cell–cell contact (34), subsequent work demonstrated that soluble factors produced by the mesenchyme regulate specific processes within the forming pancreas epithelium. Elegant work using transgenic animals identified FGF10 as one of these mesenchyme-produced factors that directly influence the developing pancreatic endoderm (35). Other mesenchyme-derived factors, such as activin, follistatin, retinoic acid, and TGF-β1, have also been shown to regulate differentiation of the pancreatic epithelium (36–39). However, until recently, the lack of suitable transgenic mouse models allowing for specific manipulation of pancreatic mesenchyme has prevented detailed studies regarding the requirement for specific mesenchymal factors (40).
Here, we set out to directly translate gene expression analysis performed on embryonic tissues to hESC to β-cell differentiation efforts. We used a precise way of isolating pancreatic mesenchyme from the epithelium using LCM, thus allowing for a direct comparison of gene expression in different tissues. Most of the 11 factors selected showed positive effects on the induction of pancreatic/foregut progenitors (Fig. 3A). From this list, we focused on two ligands from the TGF-β family, TGF-β2 and TGF-β3. TGF-βs are multifunctional cytokines that affect cell growth, differentiation, migration, and survival (24). Canonical TGF-β signaling is mediated through transmembrane serine/threonine kinase receptors. Upon ligand activation, TGF-β receptor type II (TBR II) phosphorylates and forms heterodimer with TBR type I (TBR I), also called ALK5, to initiate downstream signaling cascades via SMAD proteins (24,41). During normal pancreas development, TGF-β receptors localize to the early pancreatic epithelium as well as the mesenchyme (39). Inhibition of the TGF-β pathway using a dominant-negative receptor leads to increased endocrine differentiation and abnormal exocrine development (42,43). Although our in vitro differentiation data using TGF-β inhibition confirmed findings from these previous studies, more importantly, our analysis at earlier time points (day 7 to 9, which is approximately equivalent to E9.5 to E11.5 of mouse embryogenesis) revealed that addition of TGF-β ligands increases the number of progenitor cells and thus supports expansion of the pancreas epithelium. Our data also suggest that the TGF-β pathway is dynamically regulated to control the balance between progenitor specification and endocrine differentiation. A short activation of the pathway leads to increased expression of NGN3, whereas prolonged treatment with TGF-β ligands impairs endocrine development by keeping cells in the progenitor stage. Thus, TGF-β signaling needs to be precisely regulated to allow generation of a certain number of progenitor cells before differentiation proceeds to the next stage. A gradual shift of TGF-β receptor expression from the uncommitted epithelium to exocrine cells may indicate how this transient activation of TGF-β signaling in certain cell populations is achieved in vivo (39). Importantly, these data also point to dynamic changes in gene expression in mesenchyme throughout pancreatic development because early signals need to be downregulated to allow cell differentiation. However, it is also possible that over time, pancreatic epithelium becomes insensitive to TGF-β signaling through upregulation of inhibitory SMADs.
During mid-to-late gestation, TGF-β signaling is believed to play a role in preventing the recruitment of ductal and periductal cells into the endocrine lineage (43). In our hESC differentiation system, inhibition of the TGF-β pathway using a TGFR-I receptor antagonist significantly increased the number of insulin-producing cells, a phenomenon reminiscent of the increased accumulation of periductal endocrine cell phenotype observed in dominant-negative TBR-II receptor in mice (43).
Recently, several groups reported that inhibition of the TGF-β pathway promotes the differentiation of hESCs into hormone-producing cells in vitro (27–29). Nostro et al. (29) and Inman et al. (44) showed increased endocrine differentiation by inhibiting TGF-β/activin/nodal signaling with a small molecule ALK4/5/7 inhibitor SB431542. Afrikanova et al. (28) further reported that inhibition of Src and focal adhesion kinase promotes endocrine specification through inhibition of the TGF-βR/SMAD pathway and that addition of an ALK5 inhibitor during the PDX1 induction stage caused progenitors to exit the cell cycle. Our work supports these findings and provides novel information regarding the necessity to precisely tune the level of TGF-β signaling in a temporal manner. Activating TGF-β signaling during the pancreatic progenitor stage before inhibiting the pathway at the endocrine differentiation stage increases the number of PDX1-positive progenitor cells and induces a higher number of insulin-positive cells. Thus, our combined brief activation of the pathway, followed by inhibition of TGF-β signaling, more closely mimics the in vivo scenario in which TGF-β promotes the generation of pancreatic progenitors during earlier pancreatic differentiation but inhibits endocrine specification thereafter (43).
Interestingly, persistent TGF-β activation during the PDX1 induction phase leads to an increased number of PDX1-positive, insulin-negative cells at a later differentiation stage. Notably, we did not detect significant increases in pancreatic exocrine and duct or CDX2-marked intestinal cells under these conditions. Prolonged TGF-β inhibition after exogenous TGF-β stimulation results in a much higher number of insulin-producing cells, indicating the increased number of PDX1-positive cells represent pancreatic progenitors capable of undergoing further endocrine differentiation.
In summary, our study identified a set of mesenchymal factors that promote induction of pancreatic progenitors. When used individually, several factors, including TGF-β2, TGF-β3, FGF9, and VEGF, promote the expansion of pancreatic progenitors. In particular, the dynamic regulation of the TGF-β pathway is important for recapitulating the developmental events during progenitor expansion and endocrine specification. More detailed analysis using a combination of TGF-β ligands and some other beneficial factors identified from this study may help discover crosstalk between different signaling pathways. We anticipate that further investigation of mesenchymal factors expressed at later stages of development will help to optimize the late stages of hESC to β-cell differentiation that are currently not well recapitulated under cell culture conditions (45). In particular, it will be interesting to investigate whether the sequential TGF-β activation and inhibition also promotes differentiation of endodermal progenitor cells described recently by Gadue and colleagues (46) into fully differentiated β-cells.
Work in the laboratory of M.H. was supported by the Juvenile Diabetes Research Foundation, the Brehm Coalition, and the Leona M. and Harry B. Helmsley Charitable Trust. T.G. was supported by a postdoctoral fellowship from the Juvenile Diabetes Research Foundation. L.L. was supported by a postdoctoral fellowship from the American Diabetes Association. M.H. has equity interest in ViaCyte Inc.
No other potential conflicts of interest relevant to this article were reported.
T.G. performed the studies and assisted in the study design and its interpretation and in writing the manuscript. L.L. assisted in executing the study and study interpretation. N.L. assisted in performing the studies. M.H. contributed to the study design, study interpretation, and to preparation of the manuscript. M.H. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
The authors thank Dr. Nissim Benvenisty, of The Hebrew University of Jerusalem, for providing human islets samples and Drs. Grace Wei, Holger Ross, and Sapna Puri, of the University of California, San Francisco, for discussion and thoughtful comments on the manuscript.
This article contains Supplementary Data online at http://diabetes.diabetesjournals.org/lookup/suppl/doi:10.2337/db12-0167/-/DC1.
L.L. is currently affiliated with the Department of Cell and Developmental Biology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
- Received February 15, 2012.
- Accepted November 27, 2012.
- © 2013 by the American Diabetes Association.
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