Activation of Orphan Receptors by the Hormone Relaxin

Author:

Hsu Sheau Yu1,Nakabayashi Koji1,Nishi Shinya1,Kumagai Jin1,Kudo Masataka1,Sherwood O. David2,Hsueh Aaron J. W.1

Affiliation:

1. Division of Reproductive Biology, Department of Gynecology and Obstetrics, Stanford University School of Medicine, Stanford, CA 94305, USA.

2. Department of Molecular and Integrative Physiology, University of Illinois, Urbana-Champaign, IL 61801, USA.

Abstract

Relaxin is a hormone important for the growth and remodeling of reproductive and other tissues during pregnancy. Although binding sites for relaxin are widely distributed, the nature of its receptor has been elusive. Here, we demonstrate that two orphan heterotrimeric guanine nucleotide binding protein (G protein)–coupled receptors, LGR7 and LGR8, are capable of mediating the action of relaxin through an adenosine 3′,5′-monophosphate (cAMP)–dependent pathway distinct from that of the structurally related insulin and insulin-like growth factor family ligand. Treatment of antepartum mice with the soluble ligand-binding region of LGR7 caused parturition delay. The wide and divergent distribution of the two relaxin receptors implicates their roles in reproductive, brain, renal, cardiovascular, and other functions.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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