4.5 Article

Characterization of murine melanocortin receptors mediating adipocyte lipolysis and examination of signalling pathways involved

Journal

MOLECULAR AND CELLULAR ENDOCRINOLOGY
Volume 341, Issue 1-2, Pages 9-17

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.mce.2011.03.010

Keywords

Melanocortin receptor 1-5; Lipolysis; NEFA; Adipocytes; Real time PCR; Western blotting; Signalling; CAMP; Extracellular signal-regulated kinase (ERK); Protein kinase B (PKB); Jun-amino-terminal kinase (JNK); Adenosine 5 ' monophosphate-activated protein kinase (AMPK); 3T3-L1 cells; Isolated mouse epididymal adipocytes

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The melanocortin receptors (MCRs) belong to the G-protein coupled receptors (family A). So far, 5 different subtypes have been described (MC1R-MC5R) and of these MC2R and MC5R have been proposed to act directly in adipocytes and regulate lipolysis in rodents. Using ACTH and alpha-melanocyte stimulating hormone (alpha-MSH) generated from proopiomelanocortin (POMC), as well as synthetic MSH analogues to stimulate lipolysis in murine 3T3-L1 adipocytes it is shown that MC2R and MC5R are lipolytic mediators in differentiated 3T3-L1 adipocytes. Involvement of cAMP, phosphorylated extracellular signal-regulated kinase (ERK) 1/2, protein kinase B (PKB), adenosine 5' monophosphate activated protein kinase (AMPK) and Jun-amino-terminal kinase (INK) in MCR mediated lipolysis were studied. Interestingly, results obtained in 3T3-L1 cells suggest that lipolysis stimulated by alpha-MSH, NDP-alpha-MSH, MT-II, SHU9119 and PG-901 is mediated through MC5R in a cAMP independent manner. Finally, we identify essential differences in MCR mediated lipolysis when using 3T3-L1 cells compared to primary adipocytes. (C) 2011 Elsevier Ireland Ltd. All rights reserved.

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