瘦素
小鼠苗条素受体
能量稳态
内分泌学
内科学
岩石1
SOCS3
生物
调解人
信号转导
磷酸化
蛋白激酶A
化学
细胞生物学
车站3
医学
肥胖
作者
Huang Hu,Dong Kong,Kyung Hee Byun,Chianping Ye,Shuichi Koda,Dong Soo Lee,Byung‐Chul Oh,Sam W. Lee,Bong‐Hee Lee,Janice M. Zabolotny,Min‐Seon Kim,Christian Bjørbæk,Bradford B. Lowell,Young‐Bum Kim
摘要
Leptin regulates energy balance. However, knowledge of the critical intracellular transducers of leptin signaling remains incomplete. We found that Rho-kinase 1 (ROCK1) regulates leptin action on body weight homeostasis by activating JAK2, an initial trigger of leptin receptor signaling. Leptin promoted the physical interaction of JAK2 and ROCK1, thereby increasing phosphorylation of JAK2 and downstream activation of Stat3 and FOXO1. Mice lacking ROCK1 in either pro-opiomelanocortin (POMC) or agouti-related protein neurons, mediators of leptin action, displayed obesity and impaired leptin sensitivity. In addition, deletion of ROCK1 in the arcuate nucleus markedly enhanced food intake, resulting in severe obesity. Notably, ROCK1 was a specific mediator of leptin, but not insulin, regulation of POMC neuronal activity. Our data identify ROCK1 as a key regulator of leptin action on energy homeostasis.
科研通智能强力驱动
Strongly Powered by AbleSci AI