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G 蛋白偶联受体、Hedgehog 信号通路和初级纤毛。

G-protein-coupled receptors, Hedgehog signaling and primary cilia.

机构信息

Department of Cell Biology, UT Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.

Department of Medicine, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA; Department of Biochemistry, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA.

出版信息

Semin Cell Dev Biol. 2014 Sep;33:63-72. doi: 10.1016/j.semcdb.2014.05.002. Epub 2014 May 17.

Abstract

The Hedgehog (Hh) pathway has become an important model to study the cell biology of primary cilia, and reciprocally, the study of ciliary processes provides an opportunity to solve longstanding mysteries in the mechanism of vertebrate Hh signal transduction. The cilium is emerging as an unique compartment for G-protein-coupled receptor (GPCR) signaling in many systems. Two members of the GPCR family, Smoothened and Gpr161, play important roles in the Hh pathway. We review the current understanding of how these proteins may function to regulate Hh signaling and also highlight some of the critical unanswered questions being tackled by the field. Uncovering GPCR-regulated mechanisms important in Hh signaling may provide therapeutic strategies against the Hh pathway that plays important roles in development, regeneration and cancer.

摘要

刺猬(Hh)信号通路已成为研究初级纤毛细胞生物学的重要模型,反之亦然,纤毛过程的研究为解决脊椎动物 Hh 信号转导机制中的长期谜团提供了机会。纤毛作为许多系统中 G 蛋白偶联受体(GPCR)信号转导的独特隔室而崭露头角。GPCR 家族的两个成员 Smoothened 和 Gpr161 在 Hh 通路中发挥重要作用。我们回顾了目前对这些蛋白如何发挥作用以调节 Hh 信号的理解,并强调了该领域正在解决的一些关键未解决问题。揭示 Hh 信号中重要的 GPCR 调节机制可能为针对 Hh 通路提供治疗策略,该通路在发育、再生和癌症中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba1f/4130902/767c8bdae310/nihms-603539-f0001.jpg

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