dc.contributor.authorThan, Aung
dc.contributor.authorCheng, Yiqi
dc.contributor.authorFoh, Li-Chern
dc.contributor.authorLeow, Melvin Khee-Shing
dc.contributor.authorLim, Su Chi
dc.contributor.authorChuah, Yon Jin
dc.contributor.authorKang, Yuejun
dc.contributor.authorChen, Peng
dc.date.accessioned2013-07-11T02:11:01Z
dc.date.available2013-07-11T02:11:01Z
dc.date.copyright2012en_US
dc.date.issued2012
dc.identifier.citationThan, A., Cheng, Y., Foh, L.-C., Leow, M. K.-S., Lim, S. C., Chuah, Y. J., et al. (2012). Apelin inhibits adipogenesis and lipolysis through distint molecular pathways. Molecular and Cellular Endocrinology, 362(1-2), 227-241.
dc.identifier.urihttp://hdl.handle.net/10220/11157
dc.description.abstractApelin is an adipokine secreted by adipocytes. Co-expression of apelin and apelin receptor (APJ) in adipocytes implies the autocrine regulations of apelin on adipocyte functions through yet unknown molecular mechanisms. In the present study, we provide evidence that apelin, through its interaction with APJ receptor, inhibits adipogenesis of pre-adipocytes and lipolysis in mature adipocytes. The detailed molecular pathways underlying apelin signaling is proposed based on our experimental observations. Specifically, we show that apelin suppresses adipogenesis through MAPK kinase/ERK dependent pathways. And by preventing lipid droplet fragmentation, apelin inhibits basal lipolysis through AMP kinase dependent enhancement of perilipin expression and inhibits hormone-stimulated acute lipolysis through decreasing perilipin phosphorylation. Apelin induced decrease of free fatty acid release can be attributed to its dual inhibition on adipogenesis and lipolysis. This study suggests that the autocrine signaling of apelin may serve as a novel therapeutic target for obesity and other metabolic disorders.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesMolecular and cellular endocrinologyen_US
dc.rights© 2012 Elsevier Ireland Ltd.en_US
dc.titleApelin inhibits adipogenesis and lipolysis through distint molecular pathwaysen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Chemical and Biomedical Engineeringen_US
dc.identifier.doihttp://dx.doi.org/10.1016/j.mce.2012.07.002


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