Journal article

Hematopoietic cell-restricted deletion of CD36 reduces high-fat diet-induced macrophage infiltration and improves insulin signaling in adipose tissue

HT Nicholls, G Kowalski, DJ Kennedy, S Risis, LA Zaffino, N Watson, P Kanellakis, MJ Watt, A Bobik, A Bonen, M Febbraio, GI Lancaster, MA Febbraio

Diabetes | AMER DIABETES ASSOC | Published : 2011

Abstract

OBJECTIVE - The fatty acid translocase and scavenger receptor CD36 is important in the recognition and uptake of lipids. Accordingly, we hypothesized that it plays a role in saturated fatty acid-induced macrophage lipid accumulation and proinflammatory activation. RESEARCH DESIGN AND METHODS - In vitro, the effect of CD36 inhibition and deletion in lipid-induced macrophage inflammation was assessed using the putative CD36 inhibitor, sulfosuccinimidyl oleate (SSO), and bone marrow-derived macrophages from mice with (CD36KO) or without (wild-type) global deletion of CD36. To investigate whether deletion of macrophage CD36 would improve insulin sensitivity in vivo, wild-type mice were transplan..

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University of Melbourne Researchers

Grants

Awarded by National Heart, Lung, and Blood Institute


Funding Acknowledgements

This study was supported by grants from the Diabetes Australia Research Trust, the National Health and Medical Research Council of Australia (NHMRC) (project grant no. 526619 to M.A.F. G.I.L.), the American Heart Association Great Rivers Affiliate (0825685D to D.J.K.), and the National Institutes of Health (NIH P01 HL087018 to Roy L. Silverstein, supporting D.J.K. and M.F.). M.J.W. is a Senior Research Fellow and A.Bob. and M.A.F. are Principal Research Fellows of the NHMRC. D.J.K. is supported by the Lerner Research Institute's David and Lindsay Morgenthaler Endowed Fellowship.