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Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas

Multipotent epithelial cells with high Aldehyde dehydrogenase activity have been previously reported to exist in the adult pancreas. However, whether they represent true progenitor cells remains controversial. In this study, we isolated and characterized cells with ALDH activity in the adult mouse o...

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Autores principales: Socorro, Mairobys, Criscimanna, Angela, Riva, Patricia, Tandon, Manuj, Prasadan, Krishna, Guo, Ping, Humar, Abhinav, Husain, Sohail Z., Leach, Steven D., Gittes, George K., Esni, Farzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727523/
https://www.ncbi.nlm.nih.gov/pubmed/29235528
http://dx.doi.org/10.1038/s41598-017-17884-z
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author Socorro, Mairobys
Criscimanna, Angela
Riva, Patricia
Tandon, Manuj
Prasadan, Krishna
Guo, Ping
Humar, Abhinav
Husain, Sohail Z.
Leach, Steven D.
Gittes, George K.
Esni, Farzad
author_facet Socorro, Mairobys
Criscimanna, Angela
Riva, Patricia
Tandon, Manuj
Prasadan, Krishna
Guo, Ping
Humar, Abhinav
Husain, Sohail Z.
Leach, Steven D.
Gittes, George K.
Esni, Farzad
author_sort Socorro, Mairobys
collection PubMed
description Multipotent epithelial cells with high Aldehyde dehydrogenase activity have been previously reported to exist in the adult pancreas. However, whether they represent true progenitor cells remains controversial. In this study, we isolated and characterized cells with ALDH activity in the adult mouse or human pancreas during physiological conditions or injury. We found that cells with ALDH activity are abundant in the mouse pancreas during early postnatal growth, pregnancy, and in mouse models of pancreatitis and type 1 diabetes (T1D). Importantly, a similar population of cells is found abundantly in healthy children, or in patients with pancreatitis or T1D. We further demonstrate that cells with ALDH activity can commit to either endocrine or acinar lineages, and can be divided into four sub-populations based on CD90 and Ecadherin expression. Finally, our in vitro and in vivo studies show that the progeny of ALDH1(+)/CD90(−)/Ecad(−) cells residing in the adult mouse pancreas have the ability to initiate Pancreatic and duodenal homeobox (Pdx1) expression for the first time. In summary, we provide evidence for the existence of a sortable population of multipotent non-epithelial cells in the adult pancreas that can commit to the pancreatic lineage following proliferation and mesenchymal to epithelial transition (MET).
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spelling pubmed-57275232017-12-18 Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas Socorro, Mairobys Criscimanna, Angela Riva, Patricia Tandon, Manuj Prasadan, Krishna Guo, Ping Humar, Abhinav Husain, Sohail Z. Leach, Steven D. Gittes, George K. Esni, Farzad Sci Rep Article Multipotent epithelial cells with high Aldehyde dehydrogenase activity have been previously reported to exist in the adult pancreas. However, whether they represent true progenitor cells remains controversial. In this study, we isolated and characterized cells with ALDH activity in the adult mouse or human pancreas during physiological conditions or injury. We found that cells with ALDH activity are abundant in the mouse pancreas during early postnatal growth, pregnancy, and in mouse models of pancreatitis and type 1 diabetes (T1D). Importantly, a similar population of cells is found abundantly in healthy children, or in patients with pancreatitis or T1D. We further demonstrate that cells with ALDH activity can commit to either endocrine or acinar lineages, and can be divided into four sub-populations based on CD90 and Ecadherin expression. Finally, our in vitro and in vivo studies show that the progeny of ALDH1(+)/CD90(−)/Ecad(−) cells residing in the adult mouse pancreas have the ability to initiate Pancreatic and duodenal homeobox (Pdx1) expression for the first time. In summary, we provide evidence for the existence of a sortable population of multipotent non-epithelial cells in the adult pancreas that can commit to the pancreatic lineage following proliferation and mesenchymal to epithelial transition (MET). Nature Publishing Group UK 2017-12-13 /pmc/articles/PMC5727523/ /pubmed/29235528 http://dx.doi.org/10.1038/s41598-017-17884-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Socorro, Mairobys
Criscimanna, Angela
Riva, Patricia
Tandon, Manuj
Prasadan, Krishna
Guo, Ping
Humar, Abhinav
Husain, Sohail Z.
Leach, Steven D.
Gittes, George K.
Esni, Farzad
Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas
title Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas
title_full Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas
title_fullStr Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas
title_full_unstemmed Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas
title_short Identification of Newly Committed Pancreatic Cells in the Adult Mouse Pancreas
title_sort identification of newly committed pancreatic cells in the adult mouse pancreas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727523/
https://www.ncbi.nlm.nih.gov/pubmed/29235528
http://dx.doi.org/10.1038/s41598-017-17884-z
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