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衔接蛋白在巨噬细胞 toll 样受体信号通路中的重要作用。

Imperative role of adaptor proteins in macrophage toll-like receptor signaling pathways.

作者信息

Rughetti Aurelia, Bharti Shreya, Savai Rajkumar, Barmpoutsi Spyridoula, Weigert Andreas, Atre Rajat, Siddiqi Faaiza, Sharma Rahul, Khabiya Rakhi, Hirani Nik, Baig Mirza S

机构信息

Laboratory of Tumor Immunology & Cell Therapy, Department of Experimental Medicine, Policlinico Umberto I, University of Rome "Sapienza", Rome, Italy.

Department of Biosciences & Biomedical Engineering (BSBE), Indian Institute of Technology Indore (IITI), Indore, India.

出版信息

Future Sci OA. 2024 Dec 31;10(1):2387961. doi: 10.1080/20565623.2024.2387961. Epub 2024 Sep 9.

DOI:10.1080/20565623.2024.2387961
PMID:39248050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11385170/
Abstract

Macrophages are integral part of the body's defense against pathogens and serve as vital regulators of inflammation. Adaptor molecules, featuring diverse domains, intricately orchestrate the recruitment and transmission of inflammatory responses through signaling cascades. Key domains involved in macrophage polarization include Toll-like receptors (TLRs), Src Homology2 (SH2) and other small domains, alongside receptor tyrosine kinases, crucial for pathway activation. This review aims to elucidate the enigmatic role of macrophage adaptor molecules in modulating macrophage activation, emphasizing their diverse roles and potential therapeutic and investigative avenues for further exploration.

摘要

巨噬细胞是机体抵御病原体的重要组成部分,也是炎症的关键调节因子。衔接分子具有多种结构域,通过信号级联反应巧妙地协调炎症反应的募集和传递。参与巨噬细胞极化的关键结构域包括Toll样受体(TLR)、Src同源2(SH2)结构域和其他小结构域,以及对信号通路激活至关重要的受体酪氨酸激酶。本综述旨在阐明巨噬细胞衔接分子在调节巨噬细胞激活中的神秘作用,强调其多样的作用以及进一步探索的潜在治疗和研究途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/668a/11385170/9815f9251e03/IFSO_A_2387961_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/668a/11385170/9815f9251e03/IFSO_A_2387961_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/668a/11385170/9815f9251e03/IFSO_A_2387961_F0001_C.jpg

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本文引用的文献

1
Adaptor molecules mediate negative regulation of macrophage inflammatory pathways: a closer look.衔接分子介导巨噬细胞炎症途径的负调控:深入观察。
Front Immunol. 2024 Feb 28;15:1355012. doi: 10.3389/fimmu.2024.1355012. eCollection 2024.
2
Toll-like receptor-guided therapeutic intervention of human cancers: molecular and immunological perspectives. Toll 样受体导向的人类癌症治疗干预:分子和免疫学观点。
Front Immunol. 2023 Sep 26;14:1244345. doi: 10.3389/fimmu.2023.1244345. eCollection 2023.
3
Editorial: Targeting signalling pathways in inflammatory diseases.
社论:针对炎症性疾病中的信号通路
Front Immunol. 2023 Aug 1;14:1241440. doi: 10.3389/fimmu.2023.1241440. eCollection 2023.
4
Signal-transducing adaptor protein 1 (STAP1) in microglia promotes the malignant progression of glioma.信号转导衔接蛋白 1(STAP1)在小胶质细胞中促进神经胶质瘤的恶性进展。
J Neurooncol. 2023 Aug;164(1):127-139. doi: 10.1007/s11060-023-04390-8. Epub 2023 Jul 18.
5
Regulation of microRNA expression by the adaptor protein GRB2.衔接蛋白 GRB2 对 microRNA 表达的调控。
Sci Rep. 2023 Jun 16;13(1):9784. doi: 10.1038/s41598-023-36996-3.
6
Dorzolamide suppresses PKCδ -TIRAP-p38 MAPK signaling axis to dampen the inflammatory response.多佐胺抑制蛋白激酶Cδ-髓样分化因子88接头蛋白- p38丝裂原活化蛋白激酶信号轴,以减轻炎症反应。
Future Med Chem. 2023 Apr 27. doi: 10.4155/fmc-2022-0260.
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Helminth-derived biomacromolecules as therapeutic agents for treating inflammatory and infectious diseases: What lessons do we get from recent findings?寄生虫源生物大分子作为治疗炎症和传染病的治疗剂:我们能从最近的发现中得到什么启示?
Int J Biol Macromol. 2023 Jun 30;241:124649. doi: 10.1016/j.ijbiomac.2023.124649. Epub 2023 Apr 28.
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TIRAP, TRAM, and Toll-Like Receptors: The Untold Story.TIRAP、TRAM 和 Toll 样受体:不为人知的故事。
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