Department of Physiology & Biophysics, Boston University School of Medicine, Boston, MA 02118, United States; Department of Biochemistry, Boston University School of Medicine, Boston, MA 02118, United States.
Department of Physiology & Biophysics, Boston University School of Medicine, Boston, MA 02118, United States.
Prostaglandins Leukot Essent Fatty Acids. 2018 Nov;138:64-70. doi: 10.1016/j.plefa.2016.05.005. Epub 2016 May 20.
The scavenger receptor CD36 binds numerous small biomolecules, including fatty acids, and even large ligands such as oxidized LDL, for which it is considered a receptor. Although CD36 has often been postulated to "transport" fatty acids across the plasma membrane, fatty acids translocation (mass transport or kinetics) was not affected by expression of CD36 in HEK293 cells; however, esterification of fatty acids (cellular uptake) was increased. These recent results from our lab are consistent with the established mechanism of fatty acid entry into cells by passive diffusion (flip-flop) and also with the well-documented enhancement of uptake of fatty acids by CD36 in other cell types. A fascinating new discovery is that CD36 has multiple fatty acid binding sites on the extracellular domain of CD36. As illuminated by new methodologies that we have applied, these sites have high affinity and exhibit rapid exchange with the medium. In an initial study of functional consequences of binding, several dietary fatty acids enhanced uptake of oxidized LDL into HEK293 cells expressing CD36. This is the first established link between physical binding of fatty acids and a function of CD36, and has implications for obesity and atherosclerosis. New methods as those used in our study could also be applied to elucidate other functional roles of fatty acid binding to CD36.
清道夫受体 CD36 可结合许多小分子生物分子,包括脂肪酸,甚至是诸如氧化型 LDL 等大型配体,因此被认为是一种受体。尽管 CD36 常被推测为“转运”穿过质膜的脂肪酸,但脂肪酸的转位(质量转运或动力学)不受 HEK293 细胞中 CD36 表达的影响;然而,脂肪酸的酯化(细胞摄取)增加了。我们实验室最近的这些结果与脂肪酸通过被动扩散(翻转)进入细胞的既定机制一致,也与 CD36 在其他细胞类型中增强脂肪酸摄取的良好记录一致。一个引人入胜的新发现是 CD36 在 CD36 的细胞外结构域上具有多个脂肪酸结合位点。正如我们应用的新方法所阐明的那样,这些位点具有高亲和力,并与介质快速交换。在结合的功能后果的初步研究中,几种膳食脂肪酸增强了表达 CD36 的 HEK293 细胞对氧化型 LDL 的摄取。这是首次建立脂肪酸的物理结合与 CD36 功能之间的联系,并对肥胖和动脉粥样硬化有影响。我们研究中使用的新方法也可用于阐明脂肪酸与 CD36 结合的其他功能作用。