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Rap1b:一种有利于病毒感染的细胞骨架调节因子

Rap1b: A cytoskeletal regulator Advantageous to viral infection.

作者信息

Zhang Beibei, Li Shuli, Ding Juntao, Guo Jingxia, Ma Zhenghai

机构信息

Xinjiang Key Laboratory of Biological Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, Urumqi, Xinjiang, China.

Disease Prevention and Control Center of Xinjiang Production and Construction Corps, Urumqi, Xinjiang, China.

出版信息

iScience. 2024 Sep 24;27(10):111023. doi: 10.1016/j.isci.2024.111023. eCollection 2024 Oct 18.

DOI:10.1016/j.isci.2024.111023
PMID:39474066
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11519428/
Abstract

RAS-like small GTP-binding protein 1b (Rap1b) is a small GTPase involved in numerous deformation-mediated physiological processes, including viral infection, through cytoskeleton regulation on the premise of dynamic changes in the loading state of GTP or GDP. Previous studies have mainly focused on Rap1b's roles in tumor metastasis and platelet hemostasis due to their significant cytoskeleton rearrangement. The complexity of Rap1b and cytoskeleton functions has limited research on their role in viral infections, and the molecular mechanisms for drug and vaccine development targeting Rap1b remain unclear. Here, we reviewed the mechanisms used by Rap1b to sustain cancer growth through the cytoskeleton and analyzed the role of Rap1b protein in the regulation of the cytoskeleton, as well as its use to promote replication in response to viral invasion, highlighting that it may be a potential target for development of antiviral strategies.

摘要

RAS样小GTP结合蛋白1b(Rap1b)是一种小GTP酶,通过在GTP或GDP负载状态动态变化的前提下调节细胞骨架,参与包括病毒感染在内的众多变形介导的生理过程。由于其显著的细胞骨架重排,先前的研究主要集中在Rap1b在肿瘤转移和血小板止血中的作用。Rap1b和细胞骨架功能的复杂性限制了对其在病毒感染中作用的研究,针对Rap1b的药物和疫苗开发的分子机制仍不清楚。在这里,我们综述了Rap1b通过细胞骨架维持癌症生长的机制,分析了Rap1b蛋白在细胞骨架调节中的作用,以及其在应对病毒入侵时促进复制的作用,强调它可能是抗病毒策略开发的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/c677b46f3ed3/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/6e3dc3d6aaa3/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/415b3c79e12c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/24b78dc742b6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/feea0b6b3f83/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/c677b46f3ed3/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/6e3dc3d6aaa3/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/415b3c79e12c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/24b78dc742b6/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/feea0b6b3f83/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb6d/11519428/c677b46f3ed3/gr4.jpg

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J Cell Biol. 2024 Jul 1;223(7). doi: 10.1083/jcb.202309095. Epub 2024 May 15.
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Cortactin is in a complex with VE-cadherin and is required for endothelial adherens junction stability through Rap1/Rac1 activation.桩蛋白与血管内皮钙黏蛋白形成复合物,并通过 Rap1/Rac1 的激活来维持内皮细胞黏附连接的稳定性。
Sci Rep. 2024 Jan 12;14(1):1218. doi: 10.1038/s41598-024-51269-3.
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Rap1 coordinates cell-cell adhesion and cytoskeletal reorganization to drive collective cell migration in vivo.
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Curr Biol. 2023 Jul 10;33(13):2587-2601.e5. doi: 10.1016/j.cub.2023.05.009. Epub 2023 May 26.
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ConFERMing the role of talin in integrin activation and mechanosignaling.确认塔林在整合素激活和机械信号转导中的作用。
J Cell Sci. 2023 Apr 15;136(8). doi: 10.1242/jcs.260576. Epub 2023 Apr 20.
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Viruses. 2023 Mar 14;15(3):744. doi: 10.3390/v15030744.
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