St Vincent's Centre for Applied Medical Research, St Vincent's Hospital, Sydney, NSW 2010, Australia; Faculty of Medicine, University of New South Wales, Sydney, NSW 2052, Australia.
The University of Sydney, The Boden Institute of Obesity, Nutrition, Exercise & Eating Disorders, Sydney Medical School, Charles Perkins Centre, Sydney, NSW 2006, Australia.
Cell Metab. 2018 Sep 4;28(3):353-368. doi: 10.1016/j.cmet.2018.07.018.
MIC-1/GDF15 is a stress response cytokine and a distant member of the transforming growth factor beta (TGFb) superfamily, with no close relatives. It acts via a recently identified receptor called glial-derived neurotrophic factor (GDNF) receptor alpha-like (GFRAL), which is a distant orphan member of the GDNF receptor family that signals through the tyrosine kinase receptor Ret. MIC-1/GDF15 expression and serum levels rise in response to many stimuli that initiate cell stress and as part of a wide variety of disease processes, most prominently cancer and cardiovascular disease. The best documented actions of MIC-1/GDF15 are on regulation of energy homeostasis. When MIC-1/GDF15 serum levels are substantially elevated in diseases like cancer, it subverts a physiological pathway of appetite regulation to induce an anorexia/cachexia syndrome initiated by its actions on hindbrain neurons. These effects make it a potential target for the treatment of both obesity and anorexia/cachexia syndromes, disorders lacking any highly effective, readily accessible therapies.
MIC-1/GDF15 是一种应激反应细胞因子,属于转化生长因子 β(TGFβ)超家族的一个远亲,没有密切的相关蛋白。它通过最近发现的一种受体,即胶质细胞源性神经营养因子(GDNF)受体α样(GFRAL)发挥作用,GFRAL 是 GDNF 受体家族的一个远亲孤儿成员,通过酪氨酸激酶受体 Ret 信号转导。MIC-1/GDF15 的表达和血清水平会响应许多引发细胞应激的刺激而升高,并且是多种疾病过程的一部分,其中最突出的是癌症和心血管疾病。MIC-1/GDF15 的作用最有文献记载的是对能量稳态的调节。当 MIC-1/GDF15 的血清水平在癌症等疾病中显著升高时,它会颠覆食欲调节的生理途径,通过其对后脑神经元的作用诱导厌食/消耗综合征。这些作用使其成为治疗肥胖症和厌食/消耗综合征的潜在靶点,这两种疾病都缺乏高度有效、易于获得的治疗方法。