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All mixed up: defining roles for β-cell subtypes in mature islets

Following differentiation during fetal development, β cells further adapt to their postnatal role through functional maturation. While adult islets are thought to contain functionally mature β cells, recent analyses of transgenic rodent and human pancreata reveal a number of novel heterogeneity mark...

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Detalles Bibliográficos
Autores principales: Liu, Jennifer S.E., Hebrok, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358720/
https://www.ncbi.nlm.nih.gov/pubmed/28270515
http://dx.doi.org/10.1101/gad.294389.116
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author Liu, Jennifer S.E.
Hebrok, Matthias
author_facet Liu, Jennifer S.E.
Hebrok, Matthias
author_sort Liu, Jennifer S.E.
collection PubMed
description Following differentiation during fetal development, β cells further adapt to their postnatal role through functional maturation. While adult islets are thought to contain functionally mature β cells, recent analyses of transgenic rodent and human pancreata reveal a number of novel heterogeneity markers in mammalian β cells. The marked heterogeneity long after maturation raises the prospect that diverse populations harbor distinct roles aside from glucose-stimulated insulin secretion. In this review, we outline our current understanding of the β-cell maturation process, emphasize recent literature on novel heterogeneity markers, and offer perspectives on reconciling the findings from these two areas.
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spelling pubmed-53587202017-08-01 All mixed up: defining roles for β-cell subtypes in mature islets Liu, Jennifer S.E. Hebrok, Matthias Genes Dev Review Following differentiation during fetal development, β cells further adapt to their postnatal role through functional maturation. While adult islets are thought to contain functionally mature β cells, recent analyses of transgenic rodent and human pancreata reveal a number of novel heterogeneity markers in mammalian β cells. The marked heterogeneity long after maturation raises the prospect that diverse populations harbor distinct roles aside from glucose-stimulated insulin secretion. In this review, we outline our current understanding of the β-cell maturation process, emphasize recent literature on novel heterogeneity markers, and offer perspectives on reconciling the findings from these two areas. Cold Spring Harbor Laboratory Press 2017-02-01 /pmc/articles/PMC5358720/ /pubmed/28270515 http://dx.doi.org/10.1101/gad.294389.116 Text en © 2017 Liu and Hebrok; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review
Liu, Jennifer S.E.
Hebrok, Matthias
All mixed up: defining roles for β-cell subtypes in mature islets
title All mixed up: defining roles for β-cell subtypes in mature islets
title_full All mixed up: defining roles for β-cell subtypes in mature islets
title_fullStr All mixed up: defining roles for β-cell subtypes in mature islets
title_full_unstemmed All mixed up: defining roles for β-cell subtypes in mature islets
title_short All mixed up: defining roles for β-cell subtypes in mature islets
title_sort all mixed up: defining roles for β-cell subtypes in mature islets
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358720/
https://www.ncbi.nlm.nih.gov/pubmed/28270515
http://dx.doi.org/10.1101/gad.294389.116
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