Dietary lipids inhibit mitochondria transfer to macrophages to divert adipocyte-derived mitochondria into the blood

膳食脂质抑制线粒体向巨噬细胞的转移,从而使脂肪细胞来源的线粒体进入血液。

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作者:Nicholas Borcherding ,Wentong Jia ,Rocky Giwa ,Rachael L Field ,John R Moley ,Benjamin J Kopecky ,Mandy M Chan ,Bin Q Yang ,Jessica M Sabio ,Emma C Walker ,Omar Osorio ,Andrea L Bredemeyer ,Terri Pietka ,Jennifer Alexander-Brett ,Sharon Celeste Morley ,Maxim N Artyomov ,Nada A Abumrad ,Joel Schilling ,Kory Lavine ,Clair Crewe ,Jonathan R Brestoff

Abstract

Adipocytes transfer mitochondria to macrophages in white and brown adipose tissues to maintain metabolic homeostasis. In obesity, adipocyte-to-macrophage mitochondria transfer is impaired, and instead, adipocytes release mitochondria into the blood to induce a protective antioxidant response in the heart. We found that adipocyte-to-macrophage mitochondria transfer in white adipose tissue is inhibited in murine obesity elicited by a lard-based high-fat diet, but not a hydrogenated-coconut-oil-based high-fat diet, aging, or a corn-starch diet. The long-chain fatty acids enriched in lard suppress mitochondria capture by macrophages, diverting adipocyte-derived mitochondria into the blood for delivery to other organs, such as the heart. The depletion of macrophages rapidly increased the number of adipocyte-derived mitochondria in the blood. These findings suggest that dietary lipids regulate mitochondria uptake by macrophages locally in white adipose tissue to determine whether adipocyte-derived mitochondria are released into systemic circulation to support the metabolic adaptation of distant organs in response to nutrient stress.

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