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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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 |
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