ApoA-I Milano stimulates lipolysis in adipose cells independently of cAMP/PKA activation

作者:Lindahl Maria; Petrlova Jitka; Dalla Riva Jonathan; Wasserstrom Sebastian; Rippe Catarina; Domingo Espin Joan; Kotowska Dorota; Krupinska Ewa; Berggreen Christine; Jones Helena A; Sward Karl; Lagerstedt Jens O; Goransson Olga; Stenkula Karin G*
来源:The Journal of Lipid Research, 2015, 56(12): 2248-2259.
DOI:10.1194/jlr.M054767

摘要

ApoA-I, the main protein component of HDL, is suggested to be involved in metabolic homeostasis. We examined the effects of Milano, a naturally occurring ApoA-I variant, about which little mechanistic information is available. Remarkably, high-fat-fed mice treated with Milano displayed a rapid weight loss greater than ApoA-I WT treated mice, and a significantly reduced adipose tissue mass, without an inflammatory response. Further, lipolysis in adipose cells isolated from mice treated with either WT or Milano was increased. In primary rat adipose cells, Milano stimulated cholesterol efflux and increased glycerol release, independently of beta-adrenergic stimulation and phosphorylation of hormone sensitive lipase (Ser563) and perilipin (Ser522). Stimulation with Milano had a significantly greater effect on glycerol release compared with WT but similar effect on cholesterol efflux. Pharmacological inhibition or siRNA silencing of ABCA1 did not diminish Milano-stimulated lipolysis, although binding to the cell surface was decreased, as analyzed by fluorescence microscopy. Interestingly, methyl-beta-cyclodextrin, a well-described cholesterol acceptor, dose-dependently stimulated lipolysis. Together, these results suggest that decreased fat mass and increased lipolysis following Milano treatment in vivo is partly explained by a novel mechanism at the adipose cell level comprising stimulation of lipolysis independently of the canonical cAMP/protein kinase A signaling pathway.

  • 出版日期2015-12