Zhao Shui-Ping, Wu Jie, Zhang Da-Qing, Ye Hui-Jun, Liu Ling, Li Jie-Qi
Department of Cardiology, The Second Xiangya Hospital of Central South University, Middle Ren-Min Road No. 86, Changsha, Hunan 410011, PR China.
Atherosclerosis. 2004 Dec;177(2):255-62. doi: 10.1016/j.atherosclerosis.2004.07.015.
CD36 as a fatty acid transporter is predominantly expressed in adipocytes. We studied whether adipocytes could uptake and degrade OxLDL through CD36 and explored the effect of fenofibrate on OxLDL uptake in adipocytes from hypercholesterolemia rabbits.
Subcutaneous adipose tissues were collected from normal, high-cholesterol and high-cholesterol plus fenofibrate treatment rabbits for adipocytes culture. CD36 and peroxisome proliferator-activated receptor gamma (PPARgamma) mRNA expression were evaluated by RT-PCR.
Cellular expression of CD36 was confirmed during differentiation of adipose cell by RT-PCR. Upon incubation at 37 degrees C, (125)I-OxLDL was endocytosed in a dose-dependent fashion and underwent lysosomal degradation by adipocytes. In binding experiments at 4 degrees C, (125)I-OxLDL exhibited specific and saturable binding to adipocytes (K(D) = 4.2 microg/mL). The endocytic uptake and degradation of (125)I-OxLDL by adipocytes were inhibited by 56 and 54% with anti-CD36 antibody. Fenofibrate treatment enhanced the (125)I-OxLDL uptake and degradation and up-regulated CD36 mRNA expression in adipocytes and suppressed PPARgamma mRNA expression in adipose tissue from hypercholesterolemia rabbits.
CD36 plays a novel role in adipose tissues and adipocytes possibly involve in clearance of OxLDL in blood. Fenofibrate treatment improved the OxLDL uptake and degradation in adipocytes from hypercholesterolemia rabbits.
CD36作为一种脂肪酸转运蛋白,主要在脂肪细胞中表达。我们研究了脂肪细胞是否能通过CD36摄取和降解氧化型低密度脂蛋白(OxLDL),并探讨了非诺贝特对高胆固醇血症兔脂肪细胞摄取OxLDL的影响。
从正常、高胆固醇以及高胆固醇加非诺贝特治疗的兔身上采集皮下脂肪组织用于培养脂肪细胞。通过逆转录聚合酶链反应(RT-PCR)评估CD36和过氧化物酶体增殖物激活受体γ(PPARγ)mRNA的表达。
通过RT-PCR在脂肪细胞分化过程中证实了CD36的细胞表达。在37℃孵育时,脂肪细胞以剂量依赖方式内吞(125)I-OxLDL并进行溶酶体降解。在4℃的结合实验中,(125)I-OxLDL对脂肪细胞表现出特异性和饱和性结合(解离常数K(D)=4.2μg/mL)。抗CD36抗体使脂肪细胞对(125)I-OxLDL的内吞摄取和降解分别受到56%和54%的抑制。非诺贝特治疗增强了高胆固醇血症兔脂肪细胞对(125)I-OxLDL的摄取和降解,上调了脂肪细胞中CD36 mRNA的表达,并抑制了脂肪组织中PPARγ mRNA的表达。
CD36在脂肪组织和脂肪细胞中发挥新作用,可能参与血液中OxLDL的清除。非诺贝特治疗改善了高胆固醇血症兔脂肪细胞对OxLDL的摄取和降解。