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Slit/Robo 信号通路在骨代谢中的作用。

Role of Slit/Robo Signaling pathway in Bone Metabolism.

机构信息

State Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.

Department of Conservative Dentistry and Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China.

出版信息

Int J Biol Sci. 2022 Jan 9;18(3):1303-1312. doi: 10.7150/ijbs.66931. eCollection 2022.

Abstract

Slit/Robo signals were initially found to play an essential role in nerve development as axonal guidance molecules. In recent years, with in-depth study, the role of Slit/Robo in other life activities, such as tumor development, angiogenesis, cell migration, and bone homeostasis, has gradually been revealed. Bone is an organ with an active metabolism. Bone resorption and bone formation are closely related through precise spatiotemporal coordination. There is much evidence that slit, as a new bone coupling factor, can regulate bone formation and resorption. For example, Slit3 can promote bone formation and inhibit bone resorption through Robo receptors, which has excellent therapeutic potential in metabolic bone diseases. Although the conclusions of some studies are contradictory, they all affirm the vital role of Slit/Robo signaling in regulating bone metabolism. This paper reviews the research progress of Slit/Robo signaling in bone metabolism, briefly discusses the contradictions in the existing research, and puts forward the research direction of Slit/Robo in the field of bone metabolism in the future.

摘要

Slit/Robo 信号最初被发现作为轴突导向分子在神经发育中发挥重要作用。近年来,随着深入研究,Slit/Robo 在其他生命活动中的作用,如肿瘤发展、血管生成、细胞迁移和骨稳态,逐渐被揭示。骨骼是一个具有活跃代谢的器官。骨吸收和骨形成通过精确的时空协调密切相关。有大量证据表明,Slit 作为一种新的骨偶联因子,可以调节骨形成和骨吸收。例如,Slit3 通过 Robo 受体促进骨形成和抑制骨吸收,在代谢性骨疾病中具有很好的治疗潜力。尽管一些研究的结论存在矛盾,但它们都肯定了 Slit/Robo 信号在调节骨代谢中的重要作用。本文综述了 Slit/Robo 信号在骨代谢中的研究进展,简要讨论了现有研究中的矛盾,并提出了未来 Slit/Robo 在骨代谢领域的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5aaf/8771833/dce4fa2e7105/ijbsv18p1303g001.jpg

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