Arrestin Interactions During LH Receptor Desensitization

促黄体生成素（LH）受体是一个七跨膜受体，与G蛋白偶联，最典型的是G蛋白，激活腺苷酸环化酶转导第二信使信号。LH受体的信号转导被一种称为脱敏的分子机制所调节。虽然LH受体的脱敏可能涉及受体功能、G蛋白功能或下游效应物的衰减，但由于与抑制蛋白分子相关，受体无法激活各自的G蛋白似乎是导致受体脱敏的关键事件。我们实验室最近的研究已经阐明了β -抑制素与LH受体相互作用所必需的各种蛋白质，以及β -抑制素在信号转导中的潜在新作用。我假设在一个完整的细胞中，ARF核苷酸结合位点开启剂（ARNO）激活ADP核糖基化因子6 (ARF6)，导致β -arrestin-1从其膜对接位点释放。一旦释放，β -arrestin-1与活化的LH受体结合，并通过异源三聚体G蛋白抑制进一步的信号传导。然后，阻滞蛋白受体复合物招募Src和/或Grb-2启动另一条信号通路，即Akt信号通路。为了验证这一假设，我提出了三个具体目标，以阐明在LH受体激活后通过β -抑制素释放和信号转导的分子机制。

The luteinizing hormone (LH) receptor is a seven transmembrane spanning receptor coupled to G proteins, most typically Gs, which activates adenylyl cyclase to transduce a second messenger signal. Signal transduction by the LH receptor is tempered by a molecular mechanism known as desensitization. Although desensitization of the LH receptor may involve attenuation of receptor function, G protein function, or the downstream effector, the inability of receptors to activate their respective G-protein due to associations with arrestin molecules appears to be a key event leading to receptor desensitization. Recent studies from our laboratory have elucidated various proteins necessary for beta-arrestin interaction with the LH receptor and a potential new role for beta-arrestins in signal transduction. I hypothesize that within an intact cell ARF nucleotide-binding site opener (ARNO) activates ADP ribosylation factor 6 (ARF6) which leads to the release of beta-arrestin-1 from its membrane docking site. Once released, beta-arrestin-1 binds to the activated LH receptor and inhibits further signaling through heterotrimeric G proteins. The arrestin-receptor complex then recruits Src and/or Grb-2 to initiate a different signaling pathway, the Akt signaling pathway. To test this hypothesis, I propose three specific aims to clarify the molecular mechanisms involved in the release of and signal transduction via beta- arrestin following activation of the LH receptor.