Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.

Aldh1 expression is known to mark candidate progenitor populations in adult and embryonic mouse pancreas, and Aldh1 enzymatic activity has been identified as a potent regulator of pancreatic endocrine differentiation in zebrafish. However, the location and identity of Aldh1-expressing cells in zebra...

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Main Authors: Hiroki Matsuda, Michael J Parsons, Steven D Leach
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3798260?pdf=render
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spelling doaj-af6b7d15b03642c69811a8bcbdf732af2020-11-25T02:33:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7435010.1371/journal.pone.0074350Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.Hiroki MatsudaMichael J ParsonsSteven D LeachAldh1 expression is known to mark candidate progenitor populations in adult and embryonic mouse pancreas, and Aldh1 enzymatic activity has been identified as a potent regulator of pancreatic endocrine differentiation in zebrafish. However, the location and identity of Aldh1-expressing cells in zebrafish pancreas remain unknown. In this study we demonstrate that Aldh1-expressing cells are located immediately adjacent to 2F11-positive pancreatic ductal epithelial cells, and that their abundance dramatically increases during zebrafish secondary islet formation. These cells also express neurod, a marker of endocrine progenitor cells, but do not express markers of more mature endocrine cells such as pax6b or insulin. Using formal cre/lox-based lineage tracing, we further show that Aldh1-expressing pancreatic epithelial cells are the direct progeny of pancreatic notch-responsive progenitor cells, identifying them as a critical intermediate between multi-lineage progenitors and mature endocrine cells. Pharmacologic manipulation of Aldh1 enzymatic activity accelerates cell entry into the Aldh1-expressing endocrine progenitor pool, and also leads to the premature maturation of these cells, as evidenced by accelerated pax6b expression. Together, these findings suggest that Aldh1-expressing cells act as both participants and regulators of endocrine differentiation during zebrafish secondary islet formation.http://europepmc.org/articles/PMC3798260?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Hiroki Matsuda
Michael J Parsons
Steven D Leach
spellingShingle Hiroki Matsuda
Michael J Parsons
Steven D Leach
Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.
PLoS ONE
author_facet Hiroki Matsuda
Michael J Parsons
Steven D Leach
author_sort Hiroki Matsuda
title Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.
title_short Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.
title_full Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.
title_fullStr Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.
title_full_unstemmed Aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.
title_sort aldh1-expressing endocrine progenitor cells regulate secondary islet formation in larval zebrafish pancreas.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Aldh1 expression is known to mark candidate progenitor populations in adult and embryonic mouse pancreas, and Aldh1 enzymatic activity has been identified as a potent regulator of pancreatic endocrine differentiation in zebrafish. However, the location and identity of Aldh1-expressing cells in zebrafish pancreas remain unknown. In this study we demonstrate that Aldh1-expressing cells are located immediately adjacent to 2F11-positive pancreatic ductal epithelial cells, and that their abundance dramatically increases during zebrafish secondary islet formation. These cells also express neurod, a marker of endocrine progenitor cells, but do not express markers of more mature endocrine cells such as pax6b or insulin. Using formal cre/lox-based lineage tracing, we further show that Aldh1-expressing pancreatic epithelial cells are the direct progeny of pancreatic notch-responsive progenitor cells, identifying them as a critical intermediate between multi-lineage progenitors and mature endocrine cells. Pharmacologic manipulation of Aldh1 enzymatic activity accelerates cell entry into the Aldh1-expressing endocrine progenitor pool, and also leads to the premature maturation of these cells, as evidenced by accelerated pax6b expression. Together, these findings suggest that Aldh1-expressing cells act as both participants and regulators of endocrine differentiation during zebrafish secondary islet formation.
url http://europepmc.org/articles/PMC3798260?pdf=render
work_keys_str_mv AT hirokimatsuda aldh1expressingendocrineprogenitorcellsregulatesecondaryisletformationinlarvalzebrafishpancreas
AT michaeljparsons aldh1expressingendocrineprogenitorcellsregulatesecondaryisletformationinlarvalzebrafishpancreas
AT stevendleach aldh1expressingendocrineprogenitorcellsregulatesecondaryisletformationinlarvalzebrafishpancreas
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