Direct active Fyn-paxillin interaction regulates vascular smooth muscle cell migration.

Q3 Medicine
Ying Zhang, Hiroko Kishi, Sei Kobayashi
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引用次数: 1

Abstract

Vascular smooth muscle cell (VSMC) migration plays an important role in cardiovascular diseases, including atherosclerotic plaque formation and restenosis after vascular intervention. The mechanisms involved in VSMC migration are complex and have not been fully elucidated. Recently, we discovered a novel interaction, direct binding of active Fyn-paxillin at focal adhesions, which plays an important role in actin stress fiber formation and migration in VSMCs. In this review, we highlight paxillin as an intermediate signaling molecule that mediates actin stress fiber formation and VSMC migration through the Fyn/paxillin/Rho-kinase signaling pathway by directly binding to active Fyn. We also discuss the inhibition of VSMC migration by blocking the active Fyn-paxillin interaction and the potential of this interaction as a therapeutic target for cardiovascular diseases.

Abstract Image

直接活性Fyn-paxillin相互作用调节血管平滑肌细胞迁移。
血管平滑肌细胞(VSMC)迁移在心血管疾病中起重要作用,包括动脉粥样硬化斑块的形成和血管干预后的再狭窄。VSMC迁移的机制是复杂的,尚未完全阐明。最近,我们发现了一种新的相互作用,即活性Fyn-paxillin在局灶粘连处的直接结合,它在VSMCs中肌动蛋白应激纤维的形成和迁移中起重要作用。在这篇综述中,我们强调paxillin作为一种中间信号分子,通过Fyn/paxillin/ rho激酶信号通路直接结合活性Fyn,介导肌动蛋白应激纤维的形成和VSMC的迁移。我们还讨论了通过阻断Fyn-paxillin活性相互作用来抑制VSMC迁移,以及这种相互作用作为心血管疾病治疗靶点的潜力。
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来源期刊
Journal of Smooth Muscle Research
Journal of Smooth Muscle Research Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
2.30
自引率
0.00%
发文量
7
审稿时长
10 weeks
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