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pubmed-article:19910685pubmed:abstractTextApolipoprotein A-V is an important determinant of plasma triglyceride level in both humans and mice. This study showed the physiological impact of apoA-V on insulin secretion in rat pancreatic beta-cells (INS-1 cells). In order to precise the mechanism of action, binding experiments coupled to mass spectrometry were performed to identify a potential membrane receptor. Results showed an interaction between apoA-V and midkine protein. Confocal microscopy confirmed the plasma membrane co-localisation of this two-proteins after the treatment of INS-1 cells with the apo-AV recombinant protein and indicated that the cell surface midkine could be involved in apoA-V endocytosis, since these two proteins were co-translocated at the plasma membrane or in the cytosol compartment. This co-localisation is correlated with an increase in insulin secretion in a dose dependant manner during short incubation period. Reduction of midkine expression by small interfering RNA duplexes revealed a decrease in the ability of these transfected cells to secrete insulin in presence of apoA-V. Competition experiments for the apoA-V-midkine binding at the cell surface using antibody directed against midkine is able to influence INS-1 cell function as insulin secretion. Our results showed apoA-V ability to enhance insulin secretion in beta-cells and provide evidence of an internalization pathway involving the midkine as partner.lld:pubmed
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pubmed-article:19910685pubmed:copyrightInfo2009 S. Karger AG, Basel.lld:pubmed
pubmed-article:19910685pubmed:issnTypeElectroniclld:pubmed
pubmed-article:19910685pubmed:volume24lld:pubmed
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pubmed-article:19910685pubmed:pagination451-60lld:pubmed
pubmed-article:19910685pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:19910685pubmed:articleTitleApolipoprotein A-V modulates insulin secretion in pancreatic beta-cells through its interaction with midkine.lld:pubmed
pubmed-article:19910685pubmed:affiliationUniversité Lille Nord de France, Inserm, UDSL and Institut Pasteur de Lille, France. audrey.helleboid@univ-lille2.frlld:pubmed
pubmed-article:19910685pubmed:publicationTypeJournal Articlelld:pubmed
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