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Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas
Neurogenin3(+) (Ngn3(+)) progenitor cells in the developing pancreas give rise to five endocrine cell types secreting insulin, glucagon, somatostatin, pancreatic polypeptide and ghrelin. Gastrin is a hormone produced primarily by G-cells in the stomach, where it functions to stimulate acid secretion...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734289/ https://www.ncbi.nlm.nih.gov/pubmed/23940571 http://dx.doi.org/10.1371/journal.pone.0070397 |
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author | Suissa, Yaron Magenheim, Judith Stolovich-Rain, Miri Hija, Ayat Collombat, Patrick Mansouri, Ahmed Sussel, Lori Sosa-Pineda, Beatriz McCracken, Kyle Wells, James M. Heller, R. Scott Dor, Yuval Glaser, Benjamin |
author_facet | Suissa, Yaron Magenheim, Judith Stolovich-Rain, Miri Hija, Ayat Collombat, Patrick Mansouri, Ahmed Sussel, Lori Sosa-Pineda, Beatriz McCracken, Kyle Wells, James M. Heller, R. Scott Dor, Yuval Glaser, Benjamin |
author_sort | Suissa, Yaron |
collection | PubMed |
description | Neurogenin3(+) (Ngn3(+)) progenitor cells in the developing pancreas give rise to five endocrine cell types secreting insulin, glucagon, somatostatin, pancreatic polypeptide and ghrelin. Gastrin is a hormone produced primarily by G-cells in the stomach, where it functions to stimulate acid secretion by gastric parietal cells. Gastrin is expressed in the embryonic pancreas and is common in islet cell tumors, but the lineage and regulators of pancreatic gastrin(+) cells are not known. We report that gastrin is abundantly expressed in the embryonic pancreas and disappears soon after birth. Some gastrin(+) cells in the developing pancreas co-express glucagon, ghrelin or pancreatic polypeptide, but many gastrin(+) cells do not express any other islet hormone. Pancreatic gastrin(+) cells express the transcription factors Nkx6.1, Nkx2.2 and low levels of Pdx1, and derive from Ngn3(+) endocrine progenitor cells as shown by genetic lineage tracing. Using mice deficient for key transcription factors we show that gastrin expression depends on Ngn3, Nkx2.2, NeuroD1 and Arx, but not Pax4 or Pax6. Finally, gastrin expression is induced upon differentiation of human embryonic stem cells to pancreatic endocrine cells expressing insulin. Thus, gastrin(+) cells are a distinct endocrine cell type in the pancreas and an alternative fate of Ngn3+ cells. |
format | Online Article Text |
id | pubmed-3734289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37342892013-08-12 Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas Suissa, Yaron Magenheim, Judith Stolovich-Rain, Miri Hija, Ayat Collombat, Patrick Mansouri, Ahmed Sussel, Lori Sosa-Pineda, Beatriz McCracken, Kyle Wells, James M. Heller, R. Scott Dor, Yuval Glaser, Benjamin PLoS One Research Article Neurogenin3(+) (Ngn3(+)) progenitor cells in the developing pancreas give rise to five endocrine cell types secreting insulin, glucagon, somatostatin, pancreatic polypeptide and ghrelin. Gastrin is a hormone produced primarily by G-cells in the stomach, where it functions to stimulate acid secretion by gastric parietal cells. Gastrin is expressed in the embryonic pancreas and is common in islet cell tumors, but the lineage and regulators of pancreatic gastrin(+) cells are not known. We report that gastrin is abundantly expressed in the embryonic pancreas and disappears soon after birth. Some gastrin(+) cells in the developing pancreas co-express glucagon, ghrelin or pancreatic polypeptide, but many gastrin(+) cells do not express any other islet hormone. Pancreatic gastrin(+) cells express the transcription factors Nkx6.1, Nkx2.2 and low levels of Pdx1, and derive from Ngn3(+) endocrine progenitor cells as shown by genetic lineage tracing. Using mice deficient for key transcription factors we show that gastrin expression depends on Ngn3, Nkx2.2, NeuroD1 and Arx, but not Pax4 or Pax6. Finally, gastrin expression is induced upon differentiation of human embryonic stem cells to pancreatic endocrine cells expressing insulin. Thus, gastrin(+) cells are a distinct endocrine cell type in the pancreas and an alternative fate of Ngn3+ cells. Public Library of Science 2013-08-05 /pmc/articles/PMC3734289/ /pubmed/23940571 http://dx.doi.org/10.1371/journal.pone.0070397 Text en © 2013 Suissa et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Suissa, Yaron Magenheim, Judith Stolovich-Rain, Miri Hija, Ayat Collombat, Patrick Mansouri, Ahmed Sussel, Lori Sosa-Pineda, Beatriz McCracken, Kyle Wells, James M. Heller, R. Scott Dor, Yuval Glaser, Benjamin Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas |
title | Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas |
title_full | Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas |
title_fullStr | Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas |
title_full_unstemmed | Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas |
title_short | Gastrin: A Distinct Fate of Neurogenin3 Positive Progenitor Cells in the Embryonic Pancreas |
title_sort | gastrin: a distinct fate of neurogenin3 positive progenitor cells in the embryonic pancreas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734289/ https://www.ncbi.nlm.nih.gov/pubmed/23940571 http://dx.doi.org/10.1371/journal.pone.0070397 |
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