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Regulation of the Pancreatic Exocrine Differentiation Program and Morphogenesis by Onecut 1/Hnf6Summary
- Source :
- Cellular and Molecular Gastroenterology and Hepatology, Vol 7, Iss 4, Pp 841-856 (2019), Cellular and Molecular Gastroenterology and Hepatology
- Publication Year :
- 2019
- Publisher :
- Elsevier, 2019.
-
Abstract
- Background & Aims The Onecut 1 transcription factor (Oc1, a.k.a. HNF6) promotes differentiation of endocrine and duct cells of the pancreas; however, it has no known role in acinar cell differentiation. We sought to better understand the role of Oc1 in exocrine pancreas development and to identify its direct transcriptional targets. Methods Pancreata from Oc1Δpanc (Oc1fl/fl;Pdx1-Cre) mouse embryos and neonates were analyzed morphologically. High-throughput RNA-sequencing was performed on control and Oc1-deficient pancreas; chromatin immunoprecipitation sequencing was performed on wild-type embryonic mouse pancreata to identify direct Oc1 transcriptional targets. Immunofluorescence labeling was used to confirm the RNA-sequencing /chromatin immunoprecipitation sequencing results and to further investigate the effects of Oc1 loss on acinar cells. Results Loss of Oc1 from the developing pancreatic epithelium resulted in disrupted duct and acinar cell development. RNA-sequencing revealed decreased expression of acinar cell regulatory factors (Nr5a2, Ptf1a, Gata4, Mist1) and functional genes (Amylase, Cpa1, Prss1, Spink1) at embryonic day (e) 18.5 in Oc1Δpanc samples. Approximately 1000 of the altered genes were also identified as direct Oc1 targets by chromatin immunoprecipitation sequencing, including most of the previously noted genes. By immunolabeling, we confirmed that Amylase, Mist1, and GATA4 protein levels are significantly decreased by P2, and Spink1 protein levels were significantly reduced and mislocalized. The pancreatic duct regulatory factors Hnf1β and FoxA2 were also identified as direct Oc1 targets. Conclusions These findings confirm that Oc1 is an important regulator of both duct and acinar cell development in the embryonic pancreas. Novel transcriptional targets of Oc1 have now been identified and provide clarity into the mechanisms of Oc1 transcriptional regulation in the developing exocrine pancreas. Oc1 can now be included in the gene-regulatory network of acinar cell regulatory genes. Oc1 regulates other acinar cell regulatory factors and acinar cell functional genes directly, and it can also regulate some acinar cell regulatory factors (eg, Mist1) indirectly. Oc1 therefore plays an important role in acinar cell development.<br />Graphical abstract
- Subjects :
- 0301 basic medicine
PDAC, pancreatic ductal adenocarcinoma
Acinar Cells
Epithelium
Nr5a2, nuclear receptor subfamily 5, group A, member 2
Transcriptome
Mice
0302 clinical medicine
Transcriptional regulation
Morphogenesis
MPC, multipotent pancreatic progenitor cell
Ptf1a, Pancreas transcription factor, 1a
Original Research
Gastroenterology
Gene Expression Regulation, Developmental
Cell Differentiation
Pancreas, Exocrine
Pancreas Development
Cell biology
Hepatocyte Nuclear Factor 6
medicine.anatomical_structure
Cym, Chymosin
030211 gastroenterology & hepatology
Pancreas
Inhba, Inhibin, Beta A
Sox9, SRY-related HMG-box 9
ChIP-Seq, chromatin immunoprecipitation followed by high-throughput sequencing
RNA-Seq, RNA-sequencing
Hnf6, hepatocyte nuclear factor 6
Biology
TUNEL, terminal deoxynucleotidyl transferase dUTP nick end labeling
ADM, acinar-to-ductal metaplasia
03 medical and health sciences
CK19, Cytokeratin 19
medicine
Acinar cell
Animals
Ihh, Indian hedgehog
Mist1, muscle, intestine, stomach transcription factor 1
lcsh:RC799-869
Transcription factor
Hnf1β, hepatocyte nuclear factor 1β
Cell Proliferation
Pancreatic duct
Oc1, Onecut1
Hepatology
Base Sequence
Ptch2, Patched 2
Smo, Smoothened
HH, Hedgehog
Embryo, Mammalian
Spink 1, serine protease inhibitor Kazal type 1
030104 developmental biology
Animals, Newborn
lcsh:Diseases of the digestive system. Gastroenterology
FOXA2
Pdx1, pancreatic and duodenal homeobox 1
Exocrine
Subjects
Details
- Language :
- English
- Volume :
- 7
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Cellular and Molecular Gastroenterology and Hepatology
- Accession number :
- edsair.doi.dedup.....8340f4db90d84f348eeb0763345455be