Pepino Marta Yanina, Kuda Ondrej, Samovski Dmitri, Abumrad Nada A
Department of Medicine, Center for Human Nutrition, and.
Annu Rev Nutr. 2014;34:281-303. doi: 10.1146/annurev-nutr-071812-161220. Epub 2014 May 16.
CD36 (cluster of differentiation 36) is a scavenger receptor that functions in high-affinity tissue uptake of long-chain fatty acids (FAs) and contributes under excessive fat supply to lipid accumulation and metabolic dysfunction. This review describes recent evidence regarding the CD36 FA binding site and a potential mechanism for FA transfer. It also presents the view that CD36 and FA signaling coordinate fat utilization, a view that is based on newly identified CD36 actions that involve oral fat perception, intestinal fat absorption, secretion of the peptides cholecystokinin and secretin, regulation of hepatic lipoprotein output, activation of beta oxidation by muscle, and regulation of the production of the FA-derived bioactive eicosanoids. Thus abnormalities of fat metabolism and the associated pathology might involve dysfunction of CD36-mediated signal transduction in addition to the changes in FA uptake.
CD36(分化簇36)是一种清道夫受体,在长链脂肪酸(FAs)的高亲和力组织摄取中发挥作用,并在脂肪供应过多时导致脂质积累和代谢功能障碍。本综述描述了关于CD36脂肪酸结合位点的最新证据以及脂肪酸转运的潜在机制。它还提出了CD36与脂肪酸信号传导协调脂肪利用的观点,这一观点基于新发现的CD36作用,包括口腔脂肪感知、肠道脂肪吸收、胆囊收缩素和促胰液素肽的分泌、肝脏脂蛋白输出的调节、肌肉中β氧化的激活以及脂肪酸衍生的生物活性类二十烷酸生成的调节。因此,除了脂肪酸摄取的变化外,脂肪代谢异常及相关病理可能还涉及CD36介导的信号转导功能障碍。