Department of Physiology, National University of Singapore, Singapore 117597, Singapore; Life Sciences Institute, National University of Singapore, Singapore 117456, Singapore.
Life Sciences Institute, National University of Singapore, Singapore 117456, Singapore; Department of Neuroscience, Karolinska Institute, Stockholm 17177, Sweden.
J Biol Chem. 2020 Feb 14;295(7):2034-2042. doi: 10.1074/jbc.AC119.011795. Epub 2020 Jan 9.
Prolonged cold exposure stimulates the formation of brownlike adipocytes expressing UCP1 (uncoupling-protein-1) in subcutaneous white adipose tissue which, together with classical brown adipose tissue, contributes to maintaining body temperature in mammals through nonshivering thermogenesis. The mechanisms that regulate the formation of these cells, alternatively called beige or brite adipocytes, are incompletely understood. Here we report that mice lacking CD137, a cell surface protein used in several studies as a marker for beige adipocytes, showed elevated levels of thermogenic markers, including UCP1, increased numbers of beige adipocyte precursors, and expanded UCP1-expressing cell clusters in inguinal white adipose tissue after chronic cold exposure. CD137 knockout mice also showed enhanced cold resistance. These results indicate that CD137 functions as a negative regulator of "browning" in white adipose tissue and call into question the use of this protein as a functional marker for beige adipocytes.
长期寒冷暴露会刺激表达 UCP1(解偶联蛋白-1)的棕色样脂肪细胞在皮下白色脂肪组织中的形成,这些细胞与经典的棕色脂肪组织一起通过非颤抖产热来维持哺乳动物的体温。调节这些细胞(也称为米色或 brite 脂肪细胞)形成的机制尚不完全清楚。在这里,我们报告说,缺乏 CD137 的小鼠(在几项研究中被用作米色脂肪细胞标志物的细胞表面蛋白)在慢性寒冷暴露后表现出更高水平的产热标志物,包括 UCP1、更多的米色脂肪细胞前体和扩大的 UCP1 表达细胞簇在腹股沟白色脂肪组织中。CD137 敲除小鼠也表现出增强的抗寒能力。这些结果表明 CD137 作为白色脂肪组织中“褐变”的负调节剂发挥作用,并质疑将该蛋白用作米色脂肪细胞的功能标志物。