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Gq activity-and β-arrestin-1 scaffolding-mediated ADGRG2/CFTR coupling are required for male fertility

  • Dao Lai Zhang*
  • , Yu Jing Sun
  • , Ming Liang Ma
  • , Yi Jing Wang
  • , Hui Lin
  • , Rui Rui Li
  • , Zong Lai Liang
  • , Yuan Gao
  • , Zhao Yang
  • , Dong Fang He
  • , Amy Lin
  • , Hui Mo
  • , Yu Jing Lu
  • , Meng Jing Li
  • , Wei Kong
  • , Ka Young Chung
  • , Fan Yi
  • , Jian Yuan Li
  • , Ying Ying Qin
  • , Jingxin Li
  • Alex R.B. Thomsen, Alem W. Kahsai, Zi Jiang Chen, Zhi Gang Xu, Mingyao Liu, Dali Li, Xiao Yu, Jin Peng Sun
*此作品的通讯作者
  • Shandong University
  • Binzhou Medical College
  • Duke University
  • Peking University
  • Sungkyunkwan University
  • National Research Institute for Family Planning, Beijing
  • Texas A&M University

科研成果: 期刊稿件文章同行评审

摘要

Luminal fluid reabsorption plays a fundamental role in male fertility. We demonstrated that the ubiquitous GPCR signaling proteins Gq and b-arrestin-1 are essential for fluid reabsorption because they mediate coupling between an orphan receptor ADGRG2 (GPR64) and the ion channel CFTR. A reduction in protein level or deficiency of ADGRG2, Gq or β-arrestin-1 in a mouse model led to an imbalance in pH homeostasis in the efferent ductules due to decreased constitutive CFTR currents. Efferent ductule dysfunction was rescued by the specific activation of another GPCR, AGTR2. Further mechanistic analysis revealed that β-arrestin-1 acts as a scaffold for ADGRG2/CFTR complex formation in apical membranes, whereas specific residues of ADGRG2 confer coupling specificity for different G protein subtypes, this specificity is critical for male fertility. Therefore, manipulation of the signaling components of the ADGRG2-Gq/β-arrestin-1/CFTR complex by small molecules may be an effective therapeutic strategy for male infertility.

源语言英语
文章编号e33432
期刊eLife
7
DOI
出版状态已出版 - 2 2月 2018

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