Semaphorin 3A on Osteoporosis: An Overreview of the Literature.

IF 3.3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Yueyi Zhang, Hanfen Shi, Xuan Dai, Jin Shen, Jiyuan Yin, Tianshu Xu, Gaiyue Yue, Haochen Guo, Ruiqiong Liang, Qishuang Chen, Sihua Gao, Lili Wang, Dongwei Zhang
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引用次数: 0

Abstract

Semaphorin 3A (Sema3A) is a signaling protein that has attracted increasing attention in recent years for its important role in regulating bone metabolism. In this review, we searched different databases with various combinations of keywords to analyze the effects of Sema3A on osteoporosis. Sema3A promotes bone formation and inhibits bone resorption by directly affecting the osteoblast and osteoclast or indirectly targeting the nervous system. The sympathetic nervous system may be the main link between the central nervous system and bone metabolism for Sema3A. In the peripheral nervous system, Sema3A may improve bone quality via sensory nervous innervation. In addition, estrogen is found to regulate Sema3A levels to improve bone homeostasis. Lots of Sema3A agonists have been documented to exhibit anti-osteoporotic potential in preclinical investigations. Therefore, Sema3A can be considered a novel therapeutic target for preserving bone mass, highlighting an alternative strategy for the development of anti-osteoporosis drugs.

Semaphorin 3A(Sema3A)是一种信号蛋白,近年来因其在调节骨代谢中的重要作用而日益受到关注。在这篇综述中,我们以不同的关键词组合检索了不同的数据库,以分析 Sema3A 对骨质疏松症的影响。Sema3A 通过直接影响成骨细胞和破骨细胞或间接靶向神经系统来促进骨形成和抑制骨吸收。交感神经系统可能是 Sema3A 连接中枢神经系统和骨代谢的主要环节。在外周神经系统中,Sema3A 可通过感觉神经支配改善骨质。此外,雌激素可调节 Sema3A 的水平,从而改善骨平衡。许多 Sema3A 激动剂在临床前研究中被证实具有抗骨质疏松的潜力。因此,Sema3A 可被视为保护骨量的新型治疗靶点,为开发抗骨质疏松症药物提供了另一种策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Calcified Tissue International
Calcified Tissue International 医学-内分泌学与代谢
CiteScore
8.00
自引率
2.40%
发文量
112
审稿时长
4-8 weeks
期刊介绍: Calcified Tissue International and Musculoskeletal Research publishes original research and reviews concerning the structure and function of bone, and other musculoskeletal tissues in living organisms and clinical studies of musculoskeletal disease. It includes studies of cell biology, molecular biology, intracellular signalling, and physiology, as well as research into the hormones, cytokines and other mediators that influence the musculoskeletal system. The journal also publishes clinical studies of relevance to bone disease, mineral metabolism, muscle function, and musculoskeletal interactions.
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