脂解驱动构成性活性受体GPR3的表达,以诱导脂肪热生成
Olivia Sveidahl Johansen1, Tao Ma2, Jakob Bondo Hansen2
1Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Copenhagen, Denmark; Embark Biotech ApS, Copenhagen, Denmark; Center for Adipocyte Signaling, University of Southern Denmark, Odense, Denmark.
Cell
|May 28, 2021
概括
研究人员发现了一种激活热生成脂肪细胞的新方法, 增加GPR3表达,一个构成性活跃的受体,驱动能量消耗,并无需外部连接体来对抗代谢疾病.
科学领域:
- 代谢研究
- 脂肪细胞生物学
- G蛋白结合受体信号传递
背景情况:
- 热性脂肪细胞消耗能量,通常由寒冷和β-上腺素受体激活.
- 传统的G蛋白合受体 (GPCR) 需要外部连接体来激活.
- 了解热生成的其他途径对于代谢疾病的治疗至关重要.
研究的目的:
- 研究GPCR介导脂肪热生成的新机制.
- 探索构成性活性受体GPR3在能量消耗中的作用.
- 确定GPR3激活是否可以抵消代谢疾病.
主要方法:
- 研究了GPR3的内在信号活动和Gs合.
- 评估了Gpr3转录诱导对热生成脂肪细胞的影响.
- 研究了冷和食脂肪的Gpr3表达调节.
- 研究了GPR3在人类棕色脂肪细胞中的作用.
主要成果:
- GPR3的N端赋予了内在的信号活动,导致构成性cAMP的产生.
- Gpr3的转录诱导,独立于配体,激活热生成.
- 脂肪细胞中的Gpr3表达增加导致能量消耗,并减轻小鼠的代谢疾病.
- GPR3表达通过脂解信号被冷刺激;饮食中的脂肪增强了其发热效应.
- 人类棕色脂肪细胞的GPR3调节独立于上腺体信号.
结论:
- GPR3代表了GPCR介导的热生成的非正规途径.
- 由脂解诱导的构成性活性GPR3表达提供了一个新的热生成激活机制.
- GPR3是代谢障碍的潜在治疗点.
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