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GPR37及其神经保护机制:连接骨钙素信号与脑功能

GPR37 and its neuroprotective mechanisms: bridging osteocalcin signaling and brain function.

作者信息

Bian Xuepeng, Wang Yangping, Zhang Weijie, Ye Changlin, Li Jingjing

机构信息

Department of Rehabilitation, School of International Medical Technology, Shanghai Sanda University, Shanghai, China.

Physical Education College, Shanghai University, Shanghai, China.

出版信息

Front Cell Dev Biol. 2024 Nov 20;12:1510666. doi: 10.3389/fcell.2024.1510666. eCollection 2024.

Abstract

Osteocalcin (OCN) is a hormone secreted by osteoblasts and has attracted widespread attention for its role in regulating brain function. Clinical studies indicate a positive correlation between levels of circulating OCN and cognitive performance. Indeed, lower circulating OCN has been detected in various neurodegenerative diseases (NDs), while OCN supplementation under certain conditions may improve cognitive function. GPR37, a G protein-coupled receptor, has recently been identified as a receptor for OCN. It exhibits distinct expression patterns across various brain regions and cell types, potentially influencing its functional roles within the brain. Research indicates that GPR37 regulates neuronal migration, cell proliferation, differentiation, and myelination. Furthermore, GPR37 has been shown to mitigate inflammation and apoptosis through various mechanisms, exerting neuroprotective effects. However, its regulatory influence on brain function exhibits inconsistency, highlighting a duality in its actions. Therefore, this review thoroughly summarizes the roles and mechanisms of GPR37 in modulating cellular physiological activities and its involvement in immune responses, stress reactions, and neuroprotection. It aims to enhance the understanding of how GPR37 modulates brain function and facilitate the identification of novel therapeutic targets or strategies for related diseases.

摘要

骨钙素(OCN)是一种由成骨细胞分泌的激素,因其在调节脑功能中的作用而受到广泛关注。临床研究表明,循环中的OCN水平与认知能力之间存在正相关。事实上,在各种神经退行性疾病(NDs)中已检测到较低的循环OCN水平,而在某些条件下补充OCN可能会改善认知功能。GPR37是一种G蛋白偶联受体,最近被确定为OCN的受体。它在不同脑区和细胞类型中表现出独特的表达模式,可能影响其在大脑中的功能作用。研究表明,GPR37调节神经元迁移、细胞增殖、分化和髓鞘形成。此外,GPR37已被证明可通过多种机制减轻炎症和细胞凋亡,发挥神经保护作用。然而,其对脑功能的调节影响表现出不一致性,凸显了其作用的双重性。因此,本综述全面总结了GPR37在调节细胞生理活动中的作用和机制,以及其在免疫反应、应激反应和神经保护中的参与情况。其目的是增进对GPR37如何调节脑功能的理解,并促进相关疾病新治疗靶点或策略的识别。

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