期刊
METABOLISM-CLINICAL AND EXPERIMENTAL
卷 65, 期 12, 页码 1731-1742出版社
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.metabol.2016.09.004
关键词
Aquaporin 7; Perilipin 1; Adipocyte; Glycerol; PKA
资金
- Swedish Research Council [2011-2891]
- Cancer Foundation [2010/1171, 2014/575]
- Novo Nordisk Foundation [9807]
- Olle Engkvist Byggmastare foundation
- AFA forsakring and Diabetesfonden [DIA2015-035]
- Novo Nordisk Fonden [NNF15OC0015906, NNF14OC0009807] Funding Source: researchfish
Accumulating evidence suggests that dysregulated glycerol metabolism contributes to the pathophysiology of obesity and type 2 diabetes. Glycerol efflux from adipocytes is regulated by the aquaglyceroporin AQP7, which is translocated upon hormone stimulation. Here, we propose a molecular mechanism where the AQP7 mobility in adipocytes is dependent on perilipin 1 and protein kinase A. Biochemical analyses combined with ex vivo studies in human primary adipocytes, demonstrate that perilipin 1 binds to AQP7, and that catecholamine activated protein kinase A phosphorylates the N-terminus of AQP7, thereby reducing complex formation. Together, these findings are indicative of how glycerol release is controlled in adipocytes, and may pave the way for the future design of drugs against human metabolic pathologies. (C) 2016 The Authors. Published by Elsevier Inc.
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