Leptin action via LepR-b Tyr1077 contributes to the control of energy balance and female reproduction

摘要

Leptin action in the brain signals the repletion of adipose energy stores, suppressing feeding and permitting energy expenditure on a variety of processes, including reproduction. Leptin binding to its receptor (LepR-b) promotes the tyrosine phosphorylation of three sites on LepR-b, each of which mediates distinct downstream signals. While the signals mediated by LepR-b Tyr"1"1"3"8 and Tyr"9"8"5 control important aspects of energy homeostasis and LepR-b signal attenuation, respectively, the role of the remaining LepR-b phosphorylation site (Tyr"1"0"7"7) in leptin action has not been studied. To examine the function of Tyr"1"0"7"7, we generated a ''knock-in'' mouse model expressing LepR-b ^F^1^0^7^7, which is mutant for LepR-b Tyr"1"0"7"7. Mice expressing LepR-b ^F^1^0^7^7 demonstrate modestly increased body weight and adiposity. Furthermore, females display impairments in estrous cycling. Our results suggest that signaling by LepR-b Tyr"1"0"7"7 plays a modest role in the control of metabolism by leptin, and is an important link between body adiposity and the reproductive axis.