| Literature DB >> 29298420 |
Christina Christoffersen1, Christine K Federspiel2, Anna Borup3, Pernille M Christensen2, Andreas N Madsen4, Markus Heine5, Carsten H Nielsen6, Andreas Kjaer6, Birgitte Holst4, Joerg Heeren5, Lars B Nielsen7.
Abstract
Apolipoprotein M (apoM) is the carrier of sphingosine-1-phosphate (S1P) in plasma high-density lipoproteins. S1P is a bioactive lipid interacting with five receptors (S1P1-5). We show that lack of apoM in mice increases the amount of brown adipose tissue (BAT), accelerates the clearance of postprandial triglycerides, and protects against diet-induced obesity (i.e., a phenotype similar to that induced by cold exposure or β3-adrenergic stimulation). Moreover, the data suggest that the phenotype of apoM-deficient mice is S1P dependent and reflects diminished S1P1 stimulation. The results reveal a link between the apoM/S1P axis and energy metabolism.Entities:
Keywords: apoM; apolipoproteins; brown adipose tissue; lipid metabolism; lipoproteins; sphingolipids; sphingosine-1-phosphate; triglyceride
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Year: 2018 PMID: 29298420 DOI: 10.1016/j.celrep.2017.12.029
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423