Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Xiaoxu, Shentu, Ping, Xu, Yingke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
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
_version_ 1783235146686660608
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
work_keys_str_mv AT zhouxiaoxu spatiotemporalregulatorsforinsulinstimulatedglut4vesicleexocytosis
AT shentuping spatiotemporalregulatorsforinsulinstimulatedglut4vesicleexocytosis
AT xuyingke spatiotemporalregulatorsforinsulinstimulatedglut4vesicleexocytosis