Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

SEL1L deficiency impairs growth and differentiation of pancreatic epithelial cells

BMC Developmental Biology volume 10, Article number: 19 (2010) Cite this article

Abstract

Background

The vertebrate pancreas contains islet, acinar and ductal cells. These cells derive from a transient pool of multipotent pancreatic progenitors during embryonic development. Insight into the genetic determinants regulating pancreatic organogenesis will help the development of cell-based therapies for the treatment of diabetes mellitus. Suppressor enhancer lin12/Notch 1 like (Sel1l) encodes a cytoplasmic protein that is highly expressed in the developing mouse pancreas. However, the morphological and molecular events regulated by Sel1l remain elusive.

Results

We have characterized the pancreatic phenotype of mice carrying a gene trap mutation in Sel1l. We show that Sel1l expression in the developing pancreas coincides with differentiation of the endocrine and exocrine lineages. Mice homozygous for the gene trap mutation die prenatally and display an impaired pancreatic epithelial morphology and cell differentiation. The pancreatic epithelial cells of Sel1l mutant embryos are confined to the progenitor cell state throughout the secondary transition. Pharmacological inhibition of Notch signaling partially rescues the pancreatic phenotype of Sel1l mutant embryos.

Conclusions

Together, these data suggest that Sel1l is essential for the growth and differentiation of endoderm-derived pancreatic epithelial cells during mouse embryonic development.

Background

The multiple cell types that make up the adult pancreas, including endocrine, exocrine and ductal cells, derive from a common pool of pancreatic progenitors. Pancreatic development in mice begins at embryonic day 9.5 (E9.5) with the formation of two epithelial buds on the dorsal and ventral side of the primitive gut endoderm [1]. Epithelial cells within the pancreatic buds proliferate rapidly and branch out during later embryonic days to form a complex tubular network comprised of undifferentiated multipotent progenitor cells [2, 3]. Starting at E13.5, the expanded pancreatic epithelial cells undergo an asynchronized wave of differentiation to give rise to all the differentiated cell types of the adult pancreas, including acinar cells that produce hydrolytic digestive enzymes and islet cells that secrete endocrine hormones [4, 5]. Pancreatic morphogenesis depends on a complex and yet incompletely characterized network of transcription factors. Significant efforts have been made in the past few years to understand the role of several important transcription factors, including Pdx1 [6, 7], Ptf1a [8, 9], Sox9 [10, 11]9, Ngn3 [12, 13], NeuroD1 [14, 15], Pax4 [16], Pax6 [17], Nkx2.2 [18], Nkx6.1 [19], Arx [20], Isl1 [21] and Insm1 [22]. It is generally accepted that these transcription factors coordinate pancreatic morphogenesis by functioning in concert to restrict the developmental potentials of the pancreatic progenitors in a spatial and stage-specific manner [23].

Several previous studies have underscored the importance of Notch-mediated signaling in regulating pancreatic cell proliferation and cell fate decisions through control of Ngn3 gene expression. During pancreatic development, Ngn3 is transiently expressed in a subset of the pancreatic epithelial cells. NGN3 deficiency completely abolishes formation of all the endocrine cell subtypes, suggesting Ngn3 functions as a master switch for the endocrine lineage in the pancreas. Mutations in genes encoding Notch signaling pathway components, such as DLL1 (ligand), RBP-Jk (the intracellular mediator), or HES-1 (the effector) causes expansion of Ngn3 expression in pancreatic cells and, as a result, accelerated differentiation of endocrine cells at the expense of acinar and ductal cells [13, 24, 25]. Conversely, over or persistent expression of the Notch intracellular domain (NICD), a constitutively active form of Notch receptors, or the Notch effector gene Hes1 results in diminished expression of Ngn3 and attenuated differentiation of endocrine cells [26–28]. These studies suggest that during pancreatic development Notch signaling controls the endocrine and exocrine cell fate decisions of pancreatic epithelial cells by directly regulating Ngn3 expression. Recent studies have also indicated the importance of Notch signaling in control of exocrine cell differentiation. Ectopic expression of activated NOTCH-1 prevents or significantly delays differentiation of acinar cells [26, 27].

While the role of Notch signaling in control of pancreatic cell proliferation and cell fate decisions is clearly recognized, the molecular mechanisms necessary for proper control of Notch signaling during vertebrate pancreatic development are poorly understood. Genetic and biochemical studies in invertebrates suggest that regulation of Notch signaling occurs at various levels and through multiple mechanisms [29–31]. These include stochastic and/or developmental expression of the Notch receptors and their ligands [32–34], selective receptor-ligand interactions [35, 36], intracellular protein trafficking [37] and stability of NICD [38]. Suppressor enhancer lin12 1 like (Sel1l) encodes a cytoplasmic protein that is highly conserved throughout the vertebrate kingdom [39]. RNA in situ hybridization and immunohistological analysis revealed that Sel1l is highly expressed in both the embryonic and adult pancreas [40–42]. The human Sel1l gene is located in a chromosome region that is in close proximity to a type 1 diabetes high risk locus, IDDM-11 (insulin-dependent diabetes mellitus locus 11), prompting the speculation that mutations in Sel1l may be associated with the pathogenesis of type 1 diabetes [43]. Sel-1, the C. elegans ortholog of Sel1l, was first identified in a genetic screen for mutations that suppress lin-12/Notch activity [44]. Subsequent biochemical studies demonstrated that Sel-1 negatively regulates lin-12/Notch activity by controlling lin-12/Notch turn-over [45, 46]. Based on these findings, it has been suggested that Sel1l may also function as a negative regulator for Notch signaling [47]. Recent biochemical and molecular studies in vitro revealed that Sel1l is also required for maintaining homeostasis of the endoplasmic reticulum (ER). SEL1L nucleates an ER membrane protein complex that is required for dislocation of unfolded or misfolded proteins from the ER lumen into the cytosol for degradation [48, 49].

In an attempt to decipher the developmental and physiological roles of Sel1l, we have generated and characterized mice carrying a gene trap mutation in the Sel1l gene. We report here that Sel1l expression during pancreas development coincides with differentiation of pancreatic epithelial cells into both the endocrine and exocrine lineages. Homozygous Sel1l mutant embryos exhibit an impaired pancreatic epithelial growth and branching morphology. Pharmacological inhibition of Notch signaling rescues the pancreatic phenotype of Sel1l-deficient embryos. These data are consistent with the notion that Sel1l functions as a negative regulator for Notch signaling during pancreatic organogenesis [47].

Results

Sel1l expression during mouse pancreatic development

We generated mice carrying a gene-trap insertion in the Sel1l gene. The gene trap cassette, located in intron 14, contains a β-galactosidase-neomycin (βgeo) fusion reporter gene. To determine the spatiotemporal expression pattern of Sel1l in the developing mouse pancreas, we performed immunohistological analysis of pancreatic sections from Sel1l+/βgeoembryos using antibodies against β-galactosidase (βgal) and several pancreatic proteins, including SOX9 and PDX1 (progenitor markers), insulin and glucagon (endocrine lineage markers) and amylase (exocrine lineage marker). βgal expression was first detected at E12.5 in a small number of cells located within the core of SOX9-expressing pancreatic epithelium (Fig. 1A-B). The βgal+ cells at E12.5 express either glucagon (Fig. 1C) or insulin (Fig. 1D), indicating that they were early endocrine cells. βgal expression expands significantly between E12.5 and E14.5. At E14.5, differential βgal expression was detected in the PDX1+ cells throughout the pancreatic epithelium (Fig. 1E). Epithelial cells with markedly lower βgal expression correspond to a subset of PDX1+ cells that express SOX9 (Fig. 1F). At E15.5, high βgal expression was detected in the core of the differentiating pancreas (Fig. 1G-H, asterisks). These βgal+ cells were positive either for glucagon or insulin (arrows in Fig. 1I and 1J, respectively). At birth, βgal expression was detected in both islet and acinar cells (Fig. 1K-L, asterisk and arrow, respectively). Taken together, these expression data indicate that Sel1l is selectively expressed in the differentiating or differentiated pancreatic epithelial cells.

Figure 1
figure 1

Spatiotemporal expression of Sel1l during development of the mouse pancreas. Pancreatic sections from timed Sel1l+/βgeoembryos were co-immunostained with antibodies against βGal (red) and various pancreatic markers (green) as indicated on the left side of each panel. (B and H) Magnified views of the boxed area in A and G, respectively. (A-D) βGal expression at E12.5. βGal expression begins in a small number of cells within the core pancreatic epithelium at E12.5 (A). At this stage, there is no co-expression of βGal and SOX9 (B); however, βGal is co-expressed with either glucagon (C) or insulin (D). (E-F) βGal expression at E14.5. βGal is differentially expressed in the PDX1+ cells (E). While high βGal signal was detected in the epithelial branches (arrows), no or very low Gal signal was detected in the core "duct-like" epithelium (arrowhead). These core epithelial cells correspond to the subset of PDX+ cells that express SOX9 (F). (G-J) βGal expression at E15.5. βGal expression increases markedly in the core pancreatic epithelium (G and H, asterisks). βGal co-localizes with either glucagon (I, arrows) or insulin (J, arrows). (K-L) βGal expression at postnatal day 1. βGal is expressed in both islet and acinar tissues (K, asterisk and arrow, respectively). βGal co-localizes with PDX1 in the islet tissue (L). Scale bars: (A, G, I and J) 50 μm; (B-F, K-L) 100 μm.

Full size image

SEL1L deficiency results in defective pancreatic epithelial growth and branching morphogenesis

The gene trap in Sel1l contains a strong splicing acceptor signal that efficiently blocks splicing between exon 14 and 15, resulting in a truncated Sel1l transcript. Homozygous gene trap mice (Sel1lβge/βgeo) exhibit systemic endoplasmic reticulum stress and die before E13.5 to E15.5 (Additional file 1). To determine if Sel1l is required for pancreatic epithelial growth, we performed morphometrical analysis of the developing pancreas of viable Sel1lβgeo/βgeoembryos. At E11.5, the dorsal and ventral pancreatic buds in Sel1lβgeo/βgeoembryos appeared to be closely linked (Fig. 2B), as compared to those in wild-type embryos (Fig. 2A). There was no significant difference in the pancreatic epithelial size between wild-type and Sel1lβgeo/βgeoembryos (Fig. 2E). At E13.5, the dorsal pancreatic bud of Sel1lβgeo/βgeoembryos (Fig. 2C) was clearly smaller than that of wild-type embryos (Fig. 2F). In addition, while wild-type pancreatic epithelium displayed a well-branched structure, mutant pancreatic epithelium appeared to be a simple tube of epithelial cells. TUNEL assays revealed no significant increase of apoptosis in the developing pancreas of Sel1l mutant embryos (data not shown). Immunostaining using anti-PCNA (a cell proliferation indicator) antibody indicated that the pancreatic epithelium of Sel1l mutant embryos had a significantly lower rate of cell proliferation than wild-type pancreatic epithelium (Fig. 2G). Together, these results indicate that Sel1l, while dispensable for pancreatic epithelial induction, is essential for the subsequent growth and branching morphogenesis of the pancreatic epithelial cells.

Figure 2
figure 2

Impaired pancreatic epithelial growth and branching morphogenesis in Sel1lβgeo/βgeoembryos. (A-D) Immunohistological analysis of the developing pancreas of wild-type and Sel1lβgeo/βgeoembryos at E11.5 and E13.5; the genotypes of the pancreatic sections are indicated as +/+ and -/-, respectively. The following antibodies were used: Pdx1 (A-D, green) and insulin (C-D, red). (A-B) The dorsal and ventral pancreatic buds in Sel1lβgeo/βgeoembryos are fused together. (C-D) The dorsal pancreatic bud of Sel1lβgeo/βgeoembryos exhibits a markedly reduced epithelial size and an impaired branching morphology. (E-F) Statistical analyses of estimated pancreatic epithelial sizes of wild-type and Sel1lβgeo/βgeoembryos at E11.5 (E) and E13.5 (F). Data were from three sets of wild-type and Sel1lβgeo/βgeoembryos. No significant difference in the epithelial sizes of wild-type and Sel1l-deficient pancreas at E11.5 was detected (E). At E13.5, the pancreatic epithelium of Sel1l-deficient embryos was significantly smaller (F). Scale bar: 100 μm.

Full size image

SEL1L deficiency inhibits differentiation of acinar cells and significantly attenuates differentiation of endocrine cells

We next investigated the role of Sel1l in pancreatic epithelial cell differentiation. Since the first wave of cell differentiation occurs before E12.5 and the cells generated are mostly α-cells, we analyzed glucagon expression in E11.5 Sel1lβgeo/βgeoembryos. As shown in Fig. 3A-B and 3G, comparable numbers of glucagon+ cells were observed in wild-type and Sel1lβgeo/βgeoembryos. Sel1l is thus unlikely to be required for the generation of early endocrine cells during the first transition (E9.5 to E12.5).

While the majority of Sel1lβgeo/βgeoembryos (95%) die before the initiation of the major wave of cell differentiation in the developing pancreas (E13.5), about 5% of these embryos are viable at E15.5. To determine if Sel1l is required for differentiation of pancreatic epithelial cells during the secondary transition (E13.5 to E15.5), we analyzed the expression of three pancreatic lineage markers: insulin (β-cells), glucagon (α-cells) and amylase (acinar cells) in these embryos. Significant numbers of glucagon+ and insulin+ cells were detected in wild-type embryos at E15.5 (Fig. 3C and 3E). In contrast, the numbers of glucagon+ and insulin+ cells were significantly reduced in Sel1lβgeo/βgeoembryos (Fig. 3D and 3F, 3H and 3I). Abundant amylase+ cells are present in wild-type embryos at E15.5 (Fig. 4E). In contrast, no amylase+ cells are detectable in Sel1lβgeo/βgeoembryos (Fig. 4F). Disruption of Sel1l function thus results in an impaired differentiation of both acinar and islet cells.

Figure 3
figure 3

Inhibited endocrine and exocrine cell differentiation in Sel1lβgeo/βgeoembryos. (A-F) Immunohistological analysis of the developing pancreas of Sel1l+/+ and Sel1lβgeo/βgeoembryos at E11.5 (A-B) and E15.5 (C-F); the genotypes of the pancreatic sections are indicated as "+/+" and "-/-", respectively. The following antibodies were used: Pdx1 (A-D, green), glucagon (A-D, red), insulin (E-F, red) and amylase (E-F, green). (A-B) At E11.5, Glu+ cells were detected in the pancreatic epithelium of wild-type and Sel1lβgeo/βgeoembryos in equal numbers. (C-D) At E15.5, the number of glucagon+ cells was reduced in Sel1lβgeo/βgeoembryos as compared to wild-type control. (E-F) No amylase+ cells were detected and the number of insulin+ cells was significantly reduced in Sel1lβgeo/βgeoembryos. (G-I) Statistical analyses of the numbers of glucagon+ and insulin+ cells in wild-type and Sel1lβgeo/βgeoembryos. Data were from three wild-type and three Sel1lβgeo/βgeoembryos. At E11.5, no significant difference in the number of glucagon+ cells in wild-type and Sel1lβgeo/βgeoembryos was detected (G). The number of glucagon+ and insulin+ cells was markedly lower in Sel1lβgeo/βgeoembryos than in wild-type control embryos (H and I, respectively). Scale bar: 100 μm.

Full size image

SEL1L-deficient pancreatic epithelium exhibits inhibited growth and differentiation ex vivo

To ensure that the growth and differentiation defects observed in Sel1lβgeo/βgeoembryos were not due to the effect of global embryonic growth retardation of these embryos, we studied the pancreatic phenotype of Sel1lβgeo/βgeoembryos using an organ culture system. The dorsal pancreatic bud of wild-type and Sel1lβgeo/βgeoembryos were isolated at E11.5 and cultured for 8 days. The cultured pancreatic explants were then analyzed by immunofluorescence using antibodies against PDX1 and insulin. In general, Sel1l-deficient pancreatic epithelium grows poorly (Suppl. Fig. 2B and 2D) with about half of the cultured mutant epithelia failing to form branched epithelial structures. This is in sharp contrast to the growth behavior of wild-type pancreatic epithelia, which form a branched epithelial structure (Additional file 2). The number of insulin+ cells was significantly decreased in Sel1l-deficient pancreatic explants (Fig. 4B), as compared to that in wild-type control explants (Fig. 4A). Amylase+ cells were detected in cultured Sel1l-deficient explants (Fig. 4D), although the number of amylase+ cells was significantly lower compared to that in wild-type control explants (Fig. 4C). Thus, the pancreatic epithelium of Sel1lβgeo/βgeoembryos displays impaired growth, branching morphogenesis and lineage differentiation ex vivo. These findings confirm that the pancreatic defects observed in Sel1l-deficient embryos at E15.5 are not due to the global growth retardation.

Figure 4
figure 4

Sel1l -deficient pancreatic epithelium exhibits impaired growth, branching morphology and differentiation ex vivo. Dorsal pancreatic buds of wild-type and Sel1lβgeo/βgeoembryos were isolated at E11.5 and cultured as described in Materials and Methods. The genotypes of the pancreatic explants are indicated as "+/+" and "-/-", respectively. Cultured pancreatic explants were immunostained using the indicated antibodies. Sel1l-deficient pancreatic epithelium grows poorly and displays impaired branching morphology (B and D), as compared to wild-type control explants (A and C). The number of insulin+ cells in mutant pancreatic epithelia were markedly reduced (B, arrows), as compared to the wild-type controls (A, arrows). Amylase expression was detected in Sel1l-deficient pancreatic epithelium (D, arrows), but the expression is significantly lower than that in wild-type epithelium (C, arrows). Scale bar: 100 μm.

Full size image

Pancreatic progenitor cells in SEL1L-deficient embryos at E15.5 are confined to a pluripotent progenitor state

To gain insight into the molecular basis underlying the pancreatic defects in Sel1lβgeo/βgeoembryos, we first analyzed the expression of several transcription factors important for pancreatic epithelial growth and lineage formation. Immunostaining was carried out to assess the expression of Sox9, Pdx1 and Ptf1a in E15.5 Sel1lβgeo/βgeoembryos. PDX1 expression was uniformly detected in the pancreatic epithelial cells of Sel1lβgeo/βgeoembryos (Fig. 5B). This is in sharp contrast to wild-type embryos where PDX1 expression was differentially expressed in the pancreatic epithelial cells, with high expression in a subset of the core epithelial cells and low expression in the peripheral epithelial cells (Fig. 5A, white arrow and red arrowheads, respectively). No PTF1a expression was detected in the pancreatic epithelium of Sel1lβgeo/βgeoembryos (Fig. 5B), whereas clear co-expression of PTF1a and PDX1 was detected in the proacini in the periphery of the pancreatic epithelial buds (Fig. 5A, white arrows). SOX9 was detected in approximately 20% of the PDX1+ cells in wild-type embryos (Fig. 5C, red arrows). In contrast, SOX9 expression was observed in more than 70% of the PDX1+ cells in Sel1lβgeo/βgeoembryos (Fig. 5D, asterisk). These findings are consistent with the notion that the pancreatic epithelial cells in Sel1lβgeo/βgeoembryos at E15.5 are restricted the pancreatic progenitor state.

Figure 5
figure 5

Sel1l -deficient pancreatic epithelial cells fail to commit to lineage precursors during the secondary transition. (A-D) Immunohistological analysis of the developing dorsal pancreas of wild-type and Sel1lβgeo/βgeoembryos at E15, using the indicated antibodies. The genotypes of the pancreatic sections are indicated as "+/+" and "-/-", respectively. (A-B) PTF1a is expressed in the periphery of wild-type pancreatic epithelium marking the commitment of pancreatic epithelial cells into the exocrine lineage (A, white arrows); PTF1a expression is absent in the mutant pancreas (B). Up-regulation of PDX1 expression in a subset of epithelial cells in the core of wild-type pancreatic epithelium marks the commitment of pancreatic epithelial cells into the endocrine lineage (A, red arrows); whereas PDX1 is uniformly expressed in mutant pancreatic epithelial cells (B). (C-D) SOX9 is expressed in a small population of epithelial cells in wild-type pancreatic epithelium (C, red arrows); in contrast, SOX9 mostly co-localizes with PDX1 in mutant pancreatic epithelium (D, asterisks). Scale bar: 100 μm.

Full size image

Pharmacological inhibition of Notch signaling rescues endocrine lineage formation in Sel1lβgeo/βgeoembryos

Sel1l was thought to be a negative regulator for Notch signaling [47]. Indeed, the pancreatic phenotype in Sel1lβgeo/βgeoembryos shows remarkable similarity to that of mouse or zebrafish embryos over-expressing Notch intracellular domain, the constitutively active form of Notch receptors [26, 28, 50]. We speculated that the impaired pancreatic epithelial growth and differentiation in Sel1l-deficient embryos may be due to an increased Notch signaling activity. To test this possibility, we used the γ-secretase inhibitor, DAPT (Difluorophenacetyl-al-alanyl-S-phenylglycine-t-butyl ester), to suppress Notch signaling in pancreatic explants culture. The dorsal pancreatic bud of wild-type and Sel1lβgeo/βgeoembryos was isolated at E11.5 and cultured for 8 days in the absence or presence of DAPT. At a concentration of 10 μM, DAPT did not exhibit detectable effects on the growth, branching morphology and endocrine cell differentiation of wild-type pancreatic epithelium (Fig. 6A-B and 6E). At the same concentration, however, DAPT caused a significant expansion of the SEL1L-deficient pancreatic epithelium (Fig. 6C-D). Importantly, DAPT treatment resulted in a marked increase in the number of insulin+ cells (Fig. 6D and 6F). These observations indicate that pharmacological inhibition of Notch signaling rescues, at least partially, the pancreatic epithelial growth and endocrine differentiation defects of Sel1lβgeo/βgeoembryos.

Figure 6
figure 6

DAPT treatment rescues the pancreatic phenotype of Sel1lβgeo/βgeoembryos. The dorsal pancreatic bud of wild-type (+/+) and Sel1l mutant (-/-) embryos was isolated at E11.5 and cultured for 8 days in the presence of 0.1% DMSO (control) and 10 μM of DAPT. (A-D) Immunohistological analysis of DAPT-treated and non-treated pancreatic buds with the indicated antibodies. (E-F) Quantification of insulin+ cells in DMSO and DAPT-treated pancreatic explants. DAPT did not significantly change the number of insulin+ cells in wild-type pancreatic buds (A-B and E), however, it induced a marked increase of insulin+ cells in Sel1l mutant pancreatic buds (C-D and F). Scale bar: 100 μm.

Full size image

Discussion

The genetic determinants underlying vertebrate pancreatic development are not completely understood. In the present study, we report that Sel1l expression in the developing mouse pancreas coincides with differentiation of the endocrine and exocrine lineages during the second transition. Embryos homozygous for a gene trap insertion in Sel1l display impaired pancreatic epithelial growth and differentiation. Pharmacological inhibition of Notch signaling partially rescues the pancreatic phenotype of SEL1L-deficient embryos. Together, these data provide evidence that Sel1l is required for growth and differentiation of the mammalian pancreatic epithelial cells. The underlying mechanism may be that Sel1l functions as a negative regulator for the Notch signaling pathway by facilitating degradation of the Notch intracellular domain.

Donoviel et. al. previously reported that the mouse Sel1l gene is highly transcribed in the acini of the developing pancreas at E14.5 and E17.5 [41]. We show, by immunohistological analysis of the β-galactosidase reporter in Sel1l, that Sel1l is also highly expressed in early glucagon+ and insulin+ cells (Fig. 1C and 1D, respectively) generated during the first transition period of pancreatic development [5, 51, 52]. Consistent with the Sel1l mRNA expression pattern reported by Donoviel et. al., we reveal that at E14.5 Sel1l is broadly expressed in the PDX1+ pancreatic epithelia (Fig. 1E). Interestingly, significantly lower Sel1l expression is observed in the undifferentiated pancreatic epithelial cells (Fig. 1F) that express SOX9 [10, 11]. Our findings therefore indicate that Sel1l expression is enhanced in the committed pancreatic epithelial cells or differentiated endocrine and exocrine cells.

The selective expression of Sel1l in differentiating or differentiated pancreatic epithelial cells is highly suggestive of a role for Sel1l in promoting lineage differentiation during the secondary transition. To define the role of Sel1l in pancreatic development, we characterized the pancreatic phenotype of embryos homozygous for a gene trap insertion in Sel1l. We show that wild-type and Sel1l-deficient embryos have a comparable pancreatic epithelial size at E11.5 (Fig. 2A-B and 2E), suggesting that Sel1l function is dispensable for the induction and early growth of pancreatic epithelial cells. At E13.5, however, Sel1l-deficient pancreatic epithelia are significantly smaller and display an impaired branching morphology (Fig. 2C-D and 2F). Importantly, Sel1l-deficient pancreatic epithelia at E15.5 completely lack amylase+ cells (Fig. 3F) and have significantly reduced numbers of glucagon+ and insulin+ cells (Fig. 3D and 3F, respectively). Also, by analyzing the phenotype of cultured Sel1l-deficient dorsal pancreatic epithelia, we confirmed that the pancreatic defects in Sel1l-deficient embryos are not due to the effect of global growth retardation of the Sel1l-deficient embryos (Fig. 4A-D). Together, these data strongly suggest that Sel1l plays an important role in mouse pancreatic organogenesis by facilitating differentiation of the endocrine and exocrine lineages of the pancreas.

The C. elegans ortholog of the mammalian Sel1l gene, Sel-1, was originally identified by genetic screening as a negative regulator for lin-12/Notch signaling [44, 53]. Biochemical studies have shown that Sel-1 regulates lin-12/Notch receptor turnover [45, 46]. Whether or not Sel1l has similar functions in the mammalian system remains unclear [54]. In this study, we provide two lines of evidence that suggest Sel1l also functions as a negative regulator for Notch signaling, at least in the developing mouse pancreas. First, the observed pancreatic phenotype in Sel1l mutant embryos show remarkable similarity to the pancreatic phenotype of transgenic vertebrate embryos over-expressing the Notch intracellular domain, the constitutively active form of Notch [26, 28, 50]. Second, we show that treatment of cultured Sel1l-deficient pancreatic epithelium with DAPT, a potent Notch signaling inhibitor, partially rescues the growth and differentiation defects of Sel1l-deficient pancreatic epithelium (Fig. 6D and 6F).

How does SEL1L negatively control Notch signaling in the developing mammalian pancreas is the focus of our current investigation. Genetic and biochemical evidences from other organisms such as Drsophila and C. elegans suggest that Notch signaling is regulated at multiple levels and through multiple mechanisms, including stochastical gene expression [34], selective ligand-receptor interactions [35], intracellular trafficking [37], and stability of NICD, the active form of Notch receptors [30]. Given the previous finding that mammalian NICD are ubiquitinated and degraded through both the proteasomal and lysosomal systems [55, 56], it is conceivable that Sel1l may be directly or indirectly involved in control of NICD degradation. In this regard, it is noteworthy to mention that recent biochemical data from our laboratory indicate that NICD has significantly higher protein stability in Sel1l-deficient MEF cells (data not shown). Further proof of this hypothesis will require a detailed biochemical analysis of SEL1L and Notch interactions.

Biochemical evidences from other laboratories have also underscored the importance of Sel1l in maintaining ER homeostasis. SEL1L interacts with the E3 ubiquitin ligase HRD1 to facilitate the dislocation of unfolded or misfolded proteins from the ER lumen into the cytosol for degradation [48, 49, 57–60]. Consistent with this, we have recently shown that homozygous Sel1l mutant mice develop systemic ER stress. The impact of ER stress on pancreatic epithelial proliferation and differentiation remains undefined from the current study. However, several hypothetical roles of ER stress in pancreatic organ development and growth can be proposed. First, ER stress affects global gene expression. Upon ER stress, translation is generally down to reduce production of ER client proteins. Concomitantly, transcription of genes encoding ER chaperones and ER-associated degradation (ERAD) machinery is increased. Second, ER stress blocks or reduces protein secretion by mammalian cells. This will directly affect cell signaling and cell functions. Finally, prolonged ER stress activates the signaling pathways leading to apoptosis.

Conclusions

We report that during mouse pancreatic development, Sel1l is preferentially expressed in the differentiating or differentiated pancreatic epithelial cells. Disruption of Sel1l function results in impaired endocrine lineage formation and delayed exocrine lineage differentiation. Pharmacological suppression of Notch signaling in cultured pancreatic explants partially rescues the endocrine cell differentiation defect. Our data suggest that Sel1l may regulate pancreatic epithelial growth and differentiation by suppressing Notch-mediated signaling.

Methods

Sel1l gene trap mice

The chimeric founder mouse used to generate Sel1l gene trap mice was generated by microinjection of a commercially available mouse embryonic stem (ES) cell clone, CA0017, into C57/BL6 blastocysts. This ES cell clone contains a gene trap insertion in the 14th intron of the Sel1l gene. All mice or mouse embryos were genotyped by PCR analysis of tail or toe genomic DNA using the following PCR primers:

F-Sel1l: 5'-TGGGACAGAGCGGGCTTGGAAT-3';

R-Sel1l: 5'-CACCAGGAGTCAAAGGCATCACTG-3';

R-βGeo: 5'ATTCAGGCTGCGCAACTGTTGGG-3'.

All animal experiments were performed in accordance with the Cornell Animal Care and Use Guidelines.

Histology and immunohistochemistry

Embryos or pancreatic rudiments were fixed in 4% paraformaldehyde (PFA) in PBS at 4°C for 12 hours or longer. PFA-fixed specimens were equilibrated in 30% sucrose in PBS at 4°C and embedded in O.C.T. Sections were cut at 10 μm and immunostained essentially as described [61, 62]. Briefly, tissue sections were permeabilized with 0.2% Triton X-100 in PBS for 20 min, washed 3 times in 0.1% Triton X-100 in PBS and 3 times in PBS. The permeabilized sections were pre-incubated with 5% normal donkey serum and 1% BSA in PBS at room temperature for at least 1 hour, followed by incubation in the same solution with primary antibodies at 4°C overnight. The antibody-bound sections were then washed three times in 0.1% Triton X-100 in PBS, 3 times in PBS and then incubated with secondary antibodies for 1-3 hrs at room temperature. Primary antibodies were diluted in 1% BSA in PBS as follows: rabbit anti-b-Galactosidase (Immunology Consultants Laboratory), 1:500; guinea pig anti-Pdx-1 (Abcam), 1:1000; goat anti-Pdx1 (Abcam), 1:1000; guinea pig anti-insulin (Linco), 1:1000; rabbit anti-glucagon (Covance), 1:500; goat anti-glucagon (AbD Serotec), 1:200; rabbit anti-Sox9 (gift from Dr. Michael Wegner), 1:1000; rabbit anti-Ptf1a (gift from Dr. Helena Edlund), 1:1000); and rabbit anti-amylase (Sigma), 1:500. Secondary antibodies were diluted in 1% BSA in PBS as follows: donkey anti-rabbit IgG conjugated to Cy3 (Jackson Immuno Research), 1:1000; donkey anti-guinea pig IgG conjugated to Cy2 (Jackson Immuno Research), 1:500. Fluorescence images were acquired using an Axiovert 40 microscope (Zeiss) equipped with an AxioCam camera.

Pancreatic morphometry and cell counting

Quantitative morphometry of the developing pancreas and cell counting were performed essentially as described [11]. Briefly, pancreata of age-matched wild-type and Sel1lβgeo/βgeoembryos were sectioned through and every fifth section was immunostained with anti-PDX1 or co-immunostained with anti-PDX1 and anti-Glucagon. Quantification of pancreatic epithelium area (PDX1+ area) was performed using AxioVision Imaging analysis software (version 4.6.3). The data were presented as averages ± SEM (μm2) of three independent pancreata. Statistical analysis was performed using the Student's two-sample t test and significance is regarded as p ≤ 0.05.

Pancreatic organ culture and DAPT treatment

Sel1l+/βgeomice were intercrossed to generate embryos of defined genotypes: wild-type (Sel1l+/+), heterozygous (Sel1l+/βgeo) and homozygous (Sel1lβgeo/βgeo). The day of the vaginal plug was taken as embryonic (E) day 0.5. Pancreatic bud dissection and culture were performed essentially as described [63]. Briefly, E11.5 embryos were decapitated and the dorsal pancreatic rudiment together with surrounding mesenchymal tissue was removed in PBS. The dissected pancreatic buds were rinsed once in culture medium, transferred to a fibronectin-coated 8-well LabTek chamber slide with the epithelial side touching the bottom of the slide and cultured for 72 hours in basal medium with Earle's salts (Gibco 21010-046), 1 × glutamine, 10% FBS and antibiotics. The cultured pancreatic rudiments were fixed individually for 30 minutes in 4% paraformaldehyde in PBS for immunohistological analysis. DAPT treatment of cultured pancreatic explants was performed essentially as described [64]. DAPT stock solution was prepared at a concentration of 10 mM in DMSO and was aliquoted into single-usage aliquots. For Notch inhibition experiments, pancreatic buds were cultured in complete medium containing 10 μM of DAPT. Control pancreatic buds were cultured in complete medium containing 0.1% DMSO. The DMSO or DAPT-treated pancreatic buds were briefly fixed and analyzed by immunostaining.

References

  1. Slack JM: Developmental biology of the pancreas. Development. 1995, 121: 1569-80.

    CAS  PubMed  Google Scholar 

  2. Jorgensen MC, Ahnfelt-Ronne J, Hald J, Madsen OD, Serup P, Hecksher-Sorensen J: An illustrated review of early pancreas development in the mouse. Endocr Rev. 2007, 28: 685-705. 10.1210/er.2007-0016.

    Article  PubMed  Google Scholar 

  3. Kim SK, MacDonald RJ: Signaling and transcriptional control of pancreatic organogenesis. Curr Opin Genet Dev. 2002, 12: 540-7. 10.1016/S0959-437X(02)00338-6.

    Article  CAS  PubMed  Google Scholar 

  4. Gu G, Dubauskaite J, Melton DA: Direct evidence for the pancreatic lineage NGN3+ cells are islet progenitors and are distinct from duct progenitors. Development. 2002, 129: 2447-57.

    CAS  PubMed  Google Scholar 

  5. Pictet RL, Clark WR, Williams RH, Rutter WJ: An ultrastructural analysis of the developing embryonic pancreas. Dev Biol. 1972, 29: 436-67. 10.1016/0012-1606(72)90083-8.

    Article  CAS  PubMed  Google Scholar 

  6. Ahlgren U, Jonsson J, Edlund H: The morphogenesis of the pancreatic mesenchyme is uncoupled from that of the pancreatic epithelium in IPF1/PDX1-deficient mice. Development. 1996, 122: 1409-16.

    CAS  PubMed  Google Scholar 

  7. Offield MF, Jetton TL, Labosky PA, Ray M, Stein RW, Magnuson MA, Hogan BL, Wright CV: PDX-1 is required for pancreatic outgrowth and differentiation of the rostral duodenum. Development. 1996, 122: 983-95.

    CAS  PubMed  Google Scholar 

  8. Kawaguchi Y, Cooper B, Gannon M, Ray M, MacDonald RJ, Wright CV: The role of the transcriptional regulator Ptf1a in converting intestinal to pancreatic progenitors. Nat Genet. 2002, 32: 128-34. 10.1038/ng959.

    Article  CAS  PubMed  Google Scholar 

  9. Krapp A, Knofler M, Frutiger S, Hughes GJ, Hagenbuchle O, Wellauer PK: The p48 DNA-binding subunit of transcription factor PTF1 is a new exocrine pancreas-specific basic helix-loop-helix protein. Embo J. 1996, 15: 4317-29.

    PubMed Central  CAS  PubMed  Google Scholar 

  10. Lynn FC, Smith SB, Wilson ME, Yang KY, Nekrep N, German MS: Sox9 coordinates a transcriptional network in pancreatic progenitor cells. Proc Natl Acad Sci USA. 2007, 104: 10500-5. 10.1073/pnas.0704054104.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  11. Seymour PA, Freude KK, Tran MN, Mayes EE, Jensen J, Kist R, Scherer G, Sander M: SOX9 is required for maintenance of the pancreatic progenitor cell pool. Proc Natl Acad Sci USA. 2007, 104: 1865-70. 10.1073/pnas.0609217104.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Gradwohl G, Dierich A, LeMeur M, Guillemot F: neurogenin3 is required for the development of the four endocrine cell lineages of the pancreas. Proc Natl Acad Sci USA. 2000, 97: 1607-11. 10.1073/pnas.97.4.1607.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  13. Apelqvist A, Li H, Sommer L, Beatus P, Anderson DJ, Honjo T, Hrabe de Angelis M, Lendahl U, Edlund H: Notch signalling controls pancreatic cell differentiation. Nature. 1999, 400: 877-81. 10.1038/23716.

    Article  CAS  PubMed  Google Scholar 

  14. Naya FJ, Huang HP, Qiu Y, Mutoh H, DeMayo FJ, Leiter AB, Tsai MJ: Diabetes defective pancreatic morphogenesis and abnormal enteroendocrine differentiation in BETA2/neuroD-deficient mice. Genes Dev. 1997, 11: 2323-34. 10.1101/gad.11.18.2323.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  15. Naya FJ, Stellrecht CM, Tsai MJ: Tissue-specific regulation of the insulin gene by a novel basic helix-loop-helix transcription factor. Genes Dev. 1995, 9: 1009-19. 10.1101/gad.9.8.1009.

    Article  CAS  PubMed  Google Scholar 

  16. Sosa-Pineda B, Chowdhury K, Torres M, Oliver G, Gruss P: The Pax4 gene is essential for differentiation of insulin-producing beta cells in the mammalian pancreas. Nature. 1997, 386: 399-402. 10.1038/386399a0.

    Article  CAS  PubMed  Google Scholar 

  17. St-Onge L, Sosa-Pineda B, Chowdhury K, Mansouri A, Gruss P: Pax6 is required for differentiation of glucagon-producing alpha-cells in mouse pancreas. Nature. 1997, 387: 406-9. 10.1038/387406a0.

    Article  CAS  PubMed  Google Scholar 

  18. Sussel L, Kalamaras J, Hartigan-O'Connor DJ, Meneses JJ, Pedersen RA, Rubenstein JL, German MS: Mice lacking the homeodomain transcription factor Nkx2.2 have diabetes due to arrested differentiation of pancreatic beta cells. Development. 1998, 125: 2213-21.

    CAS  PubMed  Google Scholar 

  19. Sander M, Sussel L, Conners J, Scheel D, Kalamaras J, Dela Cruz F, Schwitzgebel V, Hayes-Jordan A, German M: Homeobox gene Nkx6.1 lies downstream of Nkx2.2 in the major pathway of beta-cell formation in the pancreas. Development. 2000, 127: 5533-40.

    CAS  PubMed  Google Scholar 

  20. Collombat P, Mansouri A, Hecksher-Sorensen J, Serup P, Krull J, Gradwohl G, Gruss P: Opposing actions of Arx and Pax4 in endocrine pancreas development. Genes Dev. 2003, 17: 2591-603. 10.1101/gad.269003.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Ahlgren U, Pfaff SL, Jessell TM, Edlund T, Edlund H: Independent requirement for ISL1 in formation of pancreatic mesenchyme and islet cells. Nature. 1997, 385: 257-60. 10.1038/385257a0.

    Article  CAS  PubMed  Google Scholar 

  22. Gierl MS, Karoulias N, Wende H, Strehle M, Birchmeier C: The zinc-finger factor Insm1 (IA-1) is essential for the development of pancreatic beta cells and intestinal endocrine cells. Genes Dev. 2006, 20: 2465-78. 10.1101/gad.381806.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  23. Johansson KA, Dursun U, Jordan N, Gu G, Beermann F, Gradwohl G, Grapin-Botton A: Temporal control of neurogenin3 activity in pancreas progenitors reveals competence windows for the generation of different endocrine cell types. Dev Cell. 2007, 12: 457-65. 10.1016/j.devcel.2007.02.010.

    Article  CAS  PubMed  Google Scholar 

  24. Jensen J, Pedersen EE, Galante P, Hald J, Heller RS, Ishibashi M, Kageyama R, Guillemot F, Serup P, Madsen OD: Control of endodermal endocrine development by Hes-1. Nat Genet. 2000, 24: 36-44. 10.1038/71657.

    Article  CAS  PubMed  Google Scholar 

  25. Fujikura J, Hosoda K, Iwakura H, Tomita T, Noguchi M, Masuzaki H, Tanigaki K, Yabe D, Honjo T, Nakao K: Notch/Rbp-j signaling prevents premature endocrine and ductal cell differentiation in the pancreas. Cell Metab. 2006, 3: 59-65. 10.1016/j.cmet.2005.12.005.

    Article  CAS  PubMed  Google Scholar 

  26. Esni F, Ghosh B, Biankin AV, Lin JW, Albert MA, Yu X, MacDonald RJ, Civin CI, Real FX, Pack MA, Ball DW, Leach SD: Notch inhibits Ptf1 function and acinar cell differentiation in developing mouse and zebrafish pancreas. Development. 2004, 131: 4213-24. 10.1242/dev.01280.

    Article  CAS  PubMed  Google Scholar 

  27. Hald J, Hjorth JP, German MS, Madsen OD, Serup P, Jensen J: Activated Notch1 prevents differentiation of pancreatic acinar cells and attenuate endocrine development. Dev Biol. 2003, 260: 426-37. 10.1016/S0012-1606(03)00326-9.

    Article  CAS  PubMed  Google Scholar 

  28. Murtaugh LC, Stanger BZ, Kwan KM, Melton DA: Notch signaling controls multiple steps of pancreatic differentiation. Proc Natl Acad Sci USA. 2003, 100: 14920-5. 10.1073/pnas.2436557100.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  29. Greenwald I: LIN-12/Notch signaling: lessons from worms and flies. Genes Dev. 1998, 12: 1751-62. 10.1101/gad.12.12.1751.

    Article  CAS  PubMed  Google Scholar 

  30. Baron M, Aslam H, Flasza M, Fostier M, Higgs JE, Mazaleyrat SL, Wilkin MB: Multiple levels of Notch signal regulation (review). Mol Membr Biol. 2002, 19: 27-38. 10.1080/09687680110112929.

    Article  CAS  PubMed  Google Scholar 

  31. Justice NJ, Jan YN: Variations on the Notch pathway in neural development. Curr Opin Neurobiol. 2002, 12: 64-70. 10.1016/S0959-4388(02)00291-X.

    Article  CAS  PubMed  Google Scholar 

  32. Cormier S, Vandormael-Pournin S, Babinet C, Cohen-Tannoudji M: Developmental expression of the Notch signaling pathway genes during mouse preimplantation development. Gene Expr Patterns. 2004, 4: 713-7. 10.1016/j.modgep.2004.04.003.

    Article  CAS  PubMed  Google Scholar 

  33. Haddon C, Smithers L, Schneider-Maunoury S, Coche T, Henrique D, Lewis J: Multiple delta genes and lateral inhibition in zebrafish primary neurogenesis. Development. 1998, 125: 359-70.

    CAS  PubMed  Google Scholar 

  34. Kaern M, Elston TC, Blake WJ, Collins JJ: Stochasticity in gene expression: from theories to phenotypes. Nat Rev Genet. 2005, 6: 451-64. 10.1038/nrg1615.

    Article  CAS  PubMed  Google Scholar 

  35. Fleming RJ, Gu Y, Hukriede NA: Serrate-mediated activation of Notch is specifically blocked by the product of the gene fringe in the dorsal compartment of the Drosophila wing imaginal disc. Development. 1997, 124: 2973-81.

    CAS  PubMed  Google Scholar 

  36. Lawrence N, Klein T, Brennan K, Martinez Arias A: Structural requirements for notch signalling with delta and serrate during the development and patterning of the wing disc of Drosophila. Development. 2000, 127: 3185-95.

    CAS  PubMed  Google Scholar 

  37. Le Borgne R, Bardin A, Schweisguth F: The roles of receptor and ligand endocytosis in regulating Notch signaling. Development. 2005, 132: 1751-62. 10.1242/dev.01789.

    Article  CAS  PubMed  Google Scholar 

  38. Lai EC: Protein degradation: four E3s for the notch pathway. Curr Biol. 2002, 12: R74-8. 10.1016/S0960-9822(01)00679-0.

    Article  CAS  PubMed  Google Scholar 

  39. Biunno I, Castiglioni B, Rogozin IB, DeBellis G, Malferrari G, Cattaneo M: Cross-species conservation of SEL1L, a human pancreas-specific expressing gene. Omics. 2002, 6: 187-98. 10.1089/153623102760092788.

    Article  CAS  PubMed  Google Scholar 

  40. Biunno I, Appierto V, Cattaneo M, Leone BE, Balzano G, Socci C, Saccone S, Letizia A, Della Valle G, Sgaramella V: Isolation of a pancreas-specific gene located on human chromosome 14q31: expression analysis in human pancreatic ductal carcinomas. Genomics. 1997, 46: 284-6. 10.1006/geno.1997.5018.

    Article  CAS  PubMed  Google Scholar 

  41. Donoviel DB, Donoviel MS, Fan E, Hadjantonakis A, Bernstein A: Cloning and characterization of Sel-1l, a murine homolog of the C. elegans sel-1 gene. Mech Dev. 1998, 78: 203-7. 10.1016/S0925-4773(98)00146-4.

    Article  CAS  PubMed  Google Scholar 

  42. Su AI, Cooke MP, Ching KA, Hakak Y, Walker JR, Wiltshire T, Orth AP, Vega RG, Sapinoso LM, Moqrich A, Patapoutian A, Hampton GM, Schultz PG, Hogenesch JB: Large-scale analysis of the human and mouse transcriptomes. Proc Natl Acad Sci USA. 2002, 99: 4465-70. 10.1073/pnas.012025199.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  43. Donoviel DB, Bernstein A: SEL-1L maps to human chromosome 14, near the insulin-dependent diabetes mellitus locus 11. Genomics. 1999, 56: 232-3. 10.1006/geno.1998.5534.

    Article  CAS  PubMed  Google Scholar 

  44. Sundaram M, Greenwald I: Suppressors of a lin-12 hypomorph define genes that interact with both lin-12 and glp-1 in Caenorhabditis elegans. Genetics. 1993, 135: 765-83.

    PubMed Central  CAS  PubMed  Google Scholar 

  45. Grant B, Greenwald I: The Caenorhabditis elegans sel-1 gene, a negative regulator of lin-12 and glp-1, encodes a predicted extracellular protein. Genetics. 1996, 143: 237-47.

    PubMed Central  CAS  PubMed  Google Scholar 

  46. Grant B, Greenwald I: Structure, function, and expression of SEL-1, a negative regulator of LIN-12 and GLP-1 in C. elegans. Development. 1997, 124: 637-44.

    CAS  PubMed  Google Scholar 

  47. Rooman I, De Medts N, Baeyens L, Lardon J, De Breuck S, Heimberg H, Bouwens L: Expression of the Notch signaling pathway and effect on exocrine cell proliferation in adult rat pancreas. Am J Pathol. 2006, 169: 1206-14. 10.2353/ajpath.2006.050926.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  48. Hosokawa N, Wada I, Nagasawa K, Moriyama T, Okawa K, Nagata K: Human XTP3-B forms an endoplasmic reticulum quality control scaffold with the HRD1-SEL1L ubiquitin ligase complex and BiP. J Biol Chem. 2008, 283: 20914-24. 10.1074/jbc.M709336200.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  49. Mueller B, Lilley BN, Ploegh HL: SEL1L, the homologue of yeast Hrd3p, is involved in protein dislocation from the mammalian ER. J Cell Biol. 2006, 175: 261-70. 10.1083/jcb.200605196.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  50. Zecchin E, Filippi A, Biemar F, Tiso N, Pauls S, Ellertsdottir E, Gnugge L, Bortolussi M, Driever W, Argenton F: Distinct delta and jagged genes control sequential segregation of pancreatic cell types from precursor pools in zebrafish. Dev Biol. 2007, 301: 192-204. 10.1016/j.ydbio.2006.09.041.

    Article  CAS  PubMed  Google Scholar 

  51. Wessells NK, Evans J: Ultrastructural studies of early morphogenesis and cytodifferentiation in the embryonic mammalian pancreas. Dev Biol. 1968, 17: 413-46. 10.1016/0012-1606(68)90073-0.

    Article  CAS  PubMed  Google Scholar 

  52. Rall LB, Pictet RL, Williams RH, Rutter WJ: Early differentiation of glucagon-producing cells in embryonic pancreas: a possible developmental role for glucagon. Proc Natl Acad Sci USA. 1973, 70: 3478-82. 10.1073/pnas.70.12.3478.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  53. Sundaram M, Greenwald I: Genetic and phenotypic studies of hypomorphic lin-12 mutants in Caenorhabditis elegans. Genetics. 1993, 135: 755-63.

    PubMed Central  CAS  PubMed  Google Scholar 

  54. Chiaramonte R, Calzavara E, Basile A, Comi P, Sherbet GV: Notch signal transduction is not regulated by SEL1L in leukaemia and lymphoma cells in culture. Anticancer Res. 2002, 22: 4211-4.

    CAS  PubMed  Google Scholar 

  55. Mukherjee A, Veraksa A, Bauer A, Rosse C, Camonis J, Artavanis-Tsakonas S: Regulation of Notch signalling by non-visual beta-arrestin. Nat Cell Biol. 2005, 7: 1191-201. 10.1038/ncb1327.

    Article  PubMed  Google Scholar 

  56. Chastagner P, Israel A, Brou C: AIP4/Itch regulates Notch receptor degradation in the absence of ligand. PLoS ONE. 2008, 3: e2735-10.1371/journal.pone.0002735.

    Article  PubMed Central  PubMed  Google Scholar 

  57. Cattaneo M, Otsu M, Fagioli C, Martino S, Lotti LV, Sitia R, Biunno I: SEL1L and HRD1 are involved in the degradation of unassembled secretory Ig-mu chains. J Cell Physiol. 2008, 215: 794-802. 10.1002/jcp.21364.

    Article  CAS  PubMed  Google Scholar 

  58. Cormier JH, Tamura T, Sunryd JC, Hebert DN: EDEM1 recognition and delivery of misfolded proteins to the SEL1L-containing ERAD complex. Mol Cell. 2009, 34: 627-33. 10.1016/j.molcel.2009.05.018.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  59. Mueller B, Klemm EJ, Spooner E, Claessen JH, Ploegh HL: SEL1L nucleates a protein complex required for dislocation of misfolded glycoproteins. Proc Natl Acad Sci USA. 2008, 105: 12325-30. 10.1073/pnas.0805371105.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  60. Oresic K, Mueller B, Tortorella D: Cln6 mutants associated with neuronal ceroid lipofuscinosis are degraded in a proteasome-dependent manner. Biosci Rep. 2009, 29: 173-81. 10.1042/BSR20080143.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  61. Burlison JS, Long Q, Fujitani Y, Wright CV, Magnuson MA: Pdx-1 and Ptf1a concurrently determine fate specification of pancreatic multipotent progenitor cells. Dev Biol. 2008, 316: 74-86. 10.1016/j.ydbio.2008.01.011.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  62. Matsuoka TA, Zhao L, Artner I, Jarrett HW, Friedman D, Means A, Stein R: Members of the large Maf transcription family regulate insulin gene transcription in islet beta cells. Mol Cell Biol. 2003, 23: 6049-62. 10.1128/MCB.23.17.6049-6062.2003.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  63. Percival AC, Slack JM: Analysis of pancreatic development using a cell lineage label. Exp Cell Res. 1999, 247: 123-32. 10.1006/excr.1998.4322.

    Article  CAS  PubMed  Google Scholar 

  64. Cheng HT, Miner JH, Lin M, Tansey MG, Roth K, Kopan R: Gamma-secretase activity is dispensable for mesenchyme-to-epithelium transition but required for podocyte and proximal tubule formation in developing mouse kidney. Development. 2003, 130: 5031-42. 10.1242/dev.00697.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We thank Dr. Patrick Biggs (Sanger Institute, UK) for generously providing the CA0017 mouse ES cell line; Drs. Raymond MacDonald (The University of Texas Southwestern Medical Center), Chyio Shiota and George Gittes (The University of Pittsburgh School of Medicine) for useful information about pancreatic explants culture; Drs. Yves Boisclair and Bruce Currie (Cornell University) for stimulating discussions and critical comments during preparation of the manuscript. The financial support for this research project was provided by the College of Agricultural and Life science, Cornell University to QL.

Author information

Authors and Affiliations

  1. Department of Animal Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, NY, 14850, USA

    Shuai Li, Adam B Francisco & Qiaoming Long

  2. Department of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, 14850, USA

    Robert J Munroe & John C Schimenti

Authors
  1. Shuai Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Adam B Francisco
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Robert J Munroe
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. John C Schimenti
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Qiaoming Long
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Qiaoming Long.

Additional information

Authors' contributions

QL designed the study and prepared the manuscript. RM and JS generated the gene trap mice. SL performed the immunohistochemistry, pancreatic bud culture and DAPT rescue experiments. AF maintained the gene trap mice and performed genotyping analysis. All authors reviewed and approved the manuscript.

Electronic supplementary material

12861_2009_496_MOESM1_ESM.PDF

Additional file 1: Characterization of the gene trap allele in Sel1l. (A) Schematic representation of the wild-type (Sel1l+) and gene trap (Sel1lβgeo) allele in Sel1l. Solid black rectangles represent exons; the open box in the Sel1l- allele represents the gene trap insertion. Splicing events are indicated by dashed lines. (B) PCR analysis of genomic DNAs from wild-type (WT), heterozygous (HT) and mutant (MU) mice using the indicated Sel1l and βgeo-specific primers (arrows). The data confirm the presence of a gene trap insertion in intron 14. (C) RT-PCR analysis of RNAs from E12.5 WT, HT and MU embryos using the indicated Sel1l and βgeo-specific primers (arrows). The data indicate that the gene trap allele in Sel1l completely blocks RNA splicing between exon 14 and 15, resulting in a truncated Sel1l transcript fused in frame with βgeo transcript. (D) Schematic representation of the full-length (FL) (top) and deletion mutant (DM) SEL1L peptides generated from the wild-type and gene trap Sel1l alleles. Key protein domains are shown in colored boxes. Numbers represent amino acid positions. The gene trap allele in Sel1l generates a fusion protein containing the N-terminal 465 amino acids of SEL1L and βgeo. The mutant peptide lacks the Hrd3-like motif, the transmembrane domain, the proline-rich domain and 4 SEL1L-like repeats. (PDF 49 KB)

12861_2009_496_MOESM2_ESM.TIFF

Additional file 2: Sel1l -deficient pancreatic epithelium exhibits impaired growth, branching morphology and differentiation ex vivo. The dorsal pancreatic bud of wild-type (+/+) and Sel1lβgeo/βgeo(-/-) embryos were isolated at E11.5 and cultured as described in Materials and Methods. Cultured pancreatic explants were immunostained with the indicated antibodies. Sel1l-deficient pancreatic epithelium grows poorly and displays impaired branching morphology (B and D), as compared to wild-type control explants (A and C). Scale bar: 100 μm. (TIFF 421 KB)

Authors’ original submitted files for images

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Li, S., Francisco, A.B., Munroe, R.J. et al. SEL1L deficiency impairs growth and differentiation of pancreatic epithelial cells. BMC Dev Biol 10, 19 (2010). https://doi.org/10.1186/1471-213X-10-19

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1471-213X-10-19

Keywords

BMC Developmental Biology

ISSN: 1471-213X

Contact us