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The dynamic plasticity of insulin production in β-cells

BACKGROUND: Although the insulin-producing pancreatic β-cells are quite capable of adapting to both acute and chronic changes in metabolic demand, persistently high demand for insulin will ultimately lead to their progressive dysfunction and eventual loss. Recent and historical studies highlight the...

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Detalles Bibliográficos
Autores principales: Boland, Brandon B., Rhodes, Christopher J., Grimsby, Joseph S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605729/
https://www.ncbi.nlm.nih.gov/pubmed/28951821
http://dx.doi.org/10.1016/j.molmet.2017.04.010
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author Boland, Brandon B.
Rhodes, Christopher J.
Grimsby, Joseph S.
author_facet Boland, Brandon B.
Rhodes, Christopher J.
Grimsby, Joseph S.
author_sort Boland, Brandon B.
collection PubMed
description BACKGROUND: Although the insulin-producing pancreatic β-cells are quite capable of adapting to both acute and chronic changes in metabolic demand, persistently high demand for insulin will ultimately lead to their progressive dysfunction and eventual loss. Recent and historical studies highlight the importance of ‘resting’ the β-cell as a means of preserving functional β-cell mass. SCOPE OF REVIEW: We provide experimental evidence to highlight the remarkable plasticity for insulin production and secretion by the pancreatic β-cell alongside some clinical evidence that supports leveraging this unique ability to preserve β-cell function. MAJOR CONCLUSIONS: Treatment strategies for type 2 diabetes mellitus (T2DM) targeted towards reducing the systemic metabolic burden, rather than demanding greater insulin production from an already beleaguered β-cell, should be emphasized to maintain endogenous insulin secretory function and delay the progression of T2DM.
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spelling pubmed-56057292017-09-26 The dynamic plasticity of insulin production in β-cells Boland, Brandon B. Rhodes, Christopher J. Grimsby, Joseph S. Mol Metab Review BACKGROUND: Although the insulin-producing pancreatic β-cells are quite capable of adapting to both acute and chronic changes in metabolic demand, persistently high demand for insulin will ultimately lead to their progressive dysfunction and eventual loss. Recent and historical studies highlight the importance of ‘resting’ the β-cell as a means of preserving functional β-cell mass. SCOPE OF REVIEW: We provide experimental evidence to highlight the remarkable plasticity for insulin production and secretion by the pancreatic β-cell alongside some clinical evidence that supports leveraging this unique ability to preserve β-cell function. MAJOR CONCLUSIONS: Treatment strategies for type 2 diabetes mellitus (T2DM) targeted towards reducing the systemic metabolic burden, rather than demanding greater insulin production from an already beleaguered β-cell, should be emphasized to maintain endogenous insulin secretory function and delay the progression of T2DM. Elsevier 2017-05-04 /pmc/articles/PMC5605729/ /pubmed/28951821 http://dx.doi.org/10.1016/j.molmet.2017.04.010 Text en © 2017 MedImmune, LLC http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Boland, Brandon B.
Rhodes, Christopher J.
Grimsby, Joseph S.
The dynamic plasticity of insulin production in β-cells
title The dynamic plasticity of insulin production in β-cells
title_full The dynamic plasticity of insulin production in β-cells
title_fullStr The dynamic plasticity of insulin production in β-cells
title_full_unstemmed The dynamic plasticity of insulin production in β-cells
title_short The dynamic plasticity of insulin production in β-cells
title_sort dynamic plasticity of insulin production in β-cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605729/
https://www.ncbi.nlm.nih.gov/pubmed/28951821
http://dx.doi.org/10.1016/j.molmet.2017.04.010
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