New insights into beta cell GLP-1 receptor and cAMP signaling
File(s)1-s2.0-S0022283619305182-main.pdf (1.67 MB)
Accepted version
Author(s)
Tomas, Alejandra
Jones, Ben
Leech, Colin
Type
Journal Article
Abstract
Harnessing the translational potential of the GLP-1/GLP-1R system in pancreatic beta cells has led to the development of established GLP-1R-based therapies for the long-term preservation of beta cell function. In this review, we discuss recent advances in the current research on the GLP-1/GLP-1R system in beta cells, including the regulation of signaling by endocytic trafficking as well as the application of concepts such as signal bias, allosteric modulation, dual agonism, polymorphic receptor variants, spatial compartmentalization of cAMP signaling and new downstream signaling targets involved in the control of beta cell function.
Date Issued
2020-03-06
Date Acceptance
2019-08-13
Citation
Journal of Molecular Biology, 2020, 432 (5), pp.1347-1366
ISSN
0022-2836
Publisher
Elsevier
Start Page
1347
End Page
1366
Journal / Book Title
Journal of Molecular Biology
Volume
432
Issue
5
Copyright Statement
© 2019 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/
Sponsor
Medical Research Council (MRC)
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/31446075
PII: S0022-2836(19)30518-2
Grant Number
MR/R010676/1
Subjects
GLP-1 receptor
beta cell survival
cAMP signaling
incretin
insulin secretion
pancreatic beta cell
0304 Medicinal and Biomolecular Chemistry
0601 Biochemistry and Cell Biology
0605 Microbiology
Biochemistry & Molecular Biology
Publication Status
Published
Coverage Spatial
England
Date Publish Online
2019-08-22