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Development of the Human Pancreas From Foregut to Endocrine Commitment

Knowledge of human pancreas development underpins our interpretation and exploitation of human pluripotent stem cell (PSC) differentiation toward a β-cell fate. However, almost no information exists on the early events of human pancreatic specification in the distal foregut, bud formation, and early...

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Autores principales: Jennings, Rachel E., Berry, Andrew A., Kirkwood-Wilson, Rebecca, Roberts, Neil A., Hearn, Thomas, Salisbury, Rachel J., Blaylock, Jennifer, Piper Hanley, Karen, Hanley, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781486/
https://www.ncbi.nlm.nih.gov/pubmed/23630303
http://dx.doi.org/10.2337/db12-1479
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author Jennings, Rachel E.
Berry, Andrew A.
Kirkwood-Wilson, Rebecca
Roberts, Neil A.
Hearn, Thomas
Salisbury, Rachel J.
Blaylock, Jennifer
Piper Hanley, Karen
Hanley, Neil A.
author_facet Jennings, Rachel E.
Berry, Andrew A.
Kirkwood-Wilson, Rebecca
Roberts, Neil A.
Hearn, Thomas
Salisbury, Rachel J.
Blaylock, Jennifer
Piper Hanley, Karen
Hanley, Neil A.
author_sort Jennings, Rachel E.
collection PubMed
description Knowledge of human pancreas development underpins our interpretation and exploitation of human pluripotent stem cell (PSC) differentiation toward a β-cell fate. However, almost no information exists on the early events of human pancreatic specification in the distal foregut, bud formation, and early development. Here, we have studied the expression profiles of key lineage-specific markers to understand differentiation and morphogenetic events during human pancreas development. The notochord was adjacent to the dorsal foregut endoderm during the fourth week of development before pancreatic duodenal homeobox-1 detection. In contrast to the published data from mouse embryos, during human pancreas development, we detected only a single-phase of Neurogenin 3 (NEUROG3) expression and endocrine differentiation from approximately 8 weeks, before which Nirenberg and Kim homeobox 2.2 (NKX2.2) was not observed in the pancreatic progenitor cell population. In addition to revealing a number of disparities in timing between human and mouse development, these data, directly assembled from human tissue, allow combinations of transcription factors to define sequential stages and differentiating pancreatic cell types. The data are anticipated to provide a useful reference point for stem cell researchers looking to differentiate human PSCs in vitro toward the pancreatic β-cell so as to model human development or enable drug discovery and potential cell therapy.
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spelling pubmed-37814862014-10-01 Development of the Human Pancreas From Foregut to Endocrine Commitment Jennings, Rachel E. Berry, Andrew A. Kirkwood-Wilson, Rebecca Roberts, Neil A. Hearn, Thomas Salisbury, Rachel J. Blaylock, Jennifer Piper Hanley, Karen Hanley, Neil A. Diabetes Original Research Knowledge of human pancreas development underpins our interpretation and exploitation of human pluripotent stem cell (PSC) differentiation toward a β-cell fate. However, almost no information exists on the early events of human pancreatic specification in the distal foregut, bud formation, and early development. Here, we have studied the expression profiles of key lineage-specific markers to understand differentiation and morphogenetic events during human pancreas development. The notochord was adjacent to the dorsal foregut endoderm during the fourth week of development before pancreatic duodenal homeobox-1 detection. In contrast to the published data from mouse embryos, during human pancreas development, we detected only a single-phase of Neurogenin 3 (NEUROG3) expression and endocrine differentiation from approximately 8 weeks, before which Nirenberg and Kim homeobox 2.2 (NKX2.2) was not observed in the pancreatic progenitor cell population. In addition to revealing a number of disparities in timing between human and mouse development, these data, directly assembled from human tissue, allow combinations of transcription factors to define sequential stages and differentiating pancreatic cell types. The data are anticipated to provide a useful reference point for stem cell researchers looking to differentiate human PSCs in vitro toward the pancreatic β-cell so as to model human development or enable drug discovery and potential cell therapy. American Diabetes Association 2013-10 2013-09-17 /pmc/articles/PMC3781486/ /pubmed/23630303 http://dx.doi.org/10.2337/db12-1479 Text en © 2013 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Jennings, Rachel E.
Berry, Andrew A.
Kirkwood-Wilson, Rebecca
Roberts, Neil A.
Hearn, Thomas
Salisbury, Rachel J.
Blaylock, Jennifer
Piper Hanley, Karen
Hanley, Neil A.
Development of the Human Pancreas From Foregut to Endocrine Commitment
title Development of the Human Pancreas From Foregut to Endocrine Commitment
title_full Development of the Human Pancreas From Foregut to Endocrine Commitment
title_fullStr Development of the Human Pancreas From Foregut to Endocrine Commitment
title_full_unstemmed Development of the Human Pancreas From Foregut to Endocrine Commitment
title_short Development of the Human Pancreas From Foregut to Endocrine Commitment
title_sort development of the human pancreas from foregut to endocrine commitment
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781486/
https://www.ncbi.nlm.nih.gov/pubmed/23630303
http://dx.doi.org/10.2337/db12-1479
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