In this section
@article{Oqua:2024:10.1530/JOE-23-0335,
author = {Oqua, AI and Manchanda, Y and McGlone, ER and Jones, B and Rouse, S and Tomas, A},
doi = {10.1530/JOE-23-0335},
journal = {Journal of Endocrinology},
title = {Lipid regulation of the glucagon receptor family},
url = {http://dx.doi.org/10.1530/JOE-23-0335},
volume = {261},
year = {2024}
}
TY - JOUR
AB - The glucagon receptor family are typical class B1 G protein-coupled receptors (GPCRs) with important roles in metabolism, including the control of pancreas, brain, and liver function. As proteins with seven transmembrane domains, GPCRs are intimately in contact with lipid bilayers and therefore can be putatively regulated by interactions with their lipidic components, including cholesterol, sphingolipids, and other lipid species. Additionally, these receptors, as well as the agonists they bind to, can undergo lipid modifications, which can influence their binding capacity and/or elicit modified or biased signalling profiles. While the effect of lipids, and in particular cholesterol, has been widely studied for other GPCR classes, information about their role in regulating the glucagon receptor family is only beginning to emerge. Here we summarise our current knowledge on the effects of cholesterol modulation of glucagon receptor family signalling and trafficking profiles, as well as existing evidence for specific lipid-receptor binding and indirect effects of lipids via lipid modification of cognate agonists. Finally, we discuss the different methodologies that can be employed to study lipid-receptor interactions and summarise the importance of this area of investigation to increase our understanding of the biology of this family of metabolically relevant receptors.
AU - Oqua,AI
AU - Manchanda,Y
AU - McGlone,ER
AU - Jones,B
AU - Rouse,S
AU - Tomas,A
DO - 10.1530/JOE-23-0335
PY - 2024///
SN - 0022-0795
TI - Lipid regulation of the glucagon receptor family
T2 - Journal of Endocrinology
UR - http://dx.doi.org/10.1530/JOE-23-0335
UR - https://www.ncbi.nlm.nih.gov/pubmed/38614123
UR - http://hdl.handle.net/10044/1/111978
VL - 261
ER -
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