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Virion display reveals MD-1 as an endogenous agonist for the orphan receptor GPRC5B

delete2026-06-16
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PRE
AI
E
Eric Johansen
G
Guan‐Da Syu
Z
Zijian Wan
D
Dylan C. Sarver
M
Meng Ding
X
Xinzhong Dong
S
Shaopeng Wang
G
G. William Wong *
H
Heng Zhu *
DOI:10.1126/scisignal.adr8554delete
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Abstract

Abstract

En 中文
GPRC5B is an orphan G protein–coupled receptor (GPCR) found on adipocytes, and GPRC5B-deficient mice are resistant to high-fat diet–induced obesity and have reduced adipose inflammation. Using a virion-based GPCR expression system combined with human protein microarrays, Johansen et al. identified the macrophage glycoprotein MD-1 as a potential endogenous GPRC5B agonist. Biochemical and functional assays showed that MD-1 stimulated Gαs-dependent signaling through GPRC5B, and cell-cell contact experiments between macrophage and adipocyte cell lines in vitro showed that MD-1 stimulated lipolysis in adipocytes, suggesting that this pathway should be investigated for therapeutic potential in obesity. —John F. Foley

Journal

Science Signaling cover
Science Signaling
IF:
6.6
Papers:
3.0K
Citations:
1.4W

Organization

J
johns hopkins university school of medicine
Scholars:
534
Papers: 160
Citations: 0
A
arizona state university
Scholars:
3.0K
Papers: 1.6K
Citations: 0
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