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Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis
Insulin increases glucose uptake and storage in muscle and adipose cells, which is accomplished through the mobilization of intracellular GLUT4 storage vesicles (GSVs) to the cell surface upon stimulation. Importantly, the dysfunction of insulin-regulated GLUT4 trafficking is strongly linked with pe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5424486/ https://www.ncbi.nlm.nih.gov/pubmed/28529958 http://dx.doi.org/10.1155/2017/1683678 |
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author | Zhou, Xiaoxu Shentu, Ping Xu, Yingke |
author_facet | Zhou, Xiaoxu Shentu, Ping Xu, Yingke |
author_sort | Zhou, Xiaoxu |
collection | PubMed |
description | Insulin increases glucose uptake and storage in muscle and adipose cells, which is accomplished through the mobilization of intracellular GLUT4 storage vesicles (GSVs) to the cell surface upon stimulation. Importantly, the dysfunction of insulin-regulated GLUT4 trafficking is strongly linked with peripheral insulin resistance and type 2 diabetes in human. The insulin signaling pathway, key signaling molecules involved, and precise trafficking itinerary of GSVs are largely identified. Understanding the interaction between insulin signaling molecules and key regulatory proteins that are involved in spatiotemporal regulation of GLUT4 vesicle exocytosis is of great importance to explain the pathogenesis of diabetes and may provide new potential therapeutic targets. |
format | Online Article Text |
id | pubmed-5424486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54244862017-05-21 Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis Zhou, Xiaoxu Shentu, Ping Xu, Yingke J Diabetes Res Review Article Insulin increases glucose uptake and storage in muscle and adipose cells, which is accomplished through the mobilization of intracellular GLUT4 storage vesicles (GSVs) to the cell surface upon stimulation. Importantly, the dysfunction of insulin-regulated GLUT4 trafficking is strongly linked with peripheral insulin resistance and type 2 diabetes in human. The insulin signaling pathway, key signaling molecules involved, and precise trafficking itinerary of GSVs are largely identified. Understanding the interaction between insulin signaling molecules and key regulatory proteins that are involved in spatiotemporal regulation of GLUT4 vesicle exocytosis is of great importance to explain the pathogenesis of diabetes and may provide new potential therapeutic targets. Hindawi 2017 2017-04-25 /pmc/articles/PMC5424486/ /pubmed/28529958 http://dx.doi.org/10.1155/2017/1683678 Text en Copyright © 2017 Xiaoxu Zhou et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Zhou, Xiaoxu Shentu, Ping Xu, Yingke Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis |
title | Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis |
title_full | Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis |
title_fullStr | Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis |
title_full_unstemmed | Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis |
title_short | Spatiotemporal Regulators for Insulin-Stimulated GLUT4 Vesicle Exocytosis |
title_sort | spatiotemporal regulators for insulin-stimulated glut4 vesicle exocytosis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5424486/ https://www.ncbi.nlm.nih.gov/pubmed/28529958 http://dx.doi.org/10.1155/2017/1683678 |
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