T cell and airway smooth muscle interaction: a key driver of asthmatic airway inflammation and remodeling

被引:0
|
作者
Zhou, Muyang [1 ,2 ]
Sun, Rui [1 ,2 ]
Jang, Joyce [1 ,2 ]
Martin, James G. [1 ,2 ]
机构
[1] McGill Univ, Dept Med, Div Expt Med, Montreal, PQ, Canada
[2] McGill Univ, Res Inst, Hlth Ctr, Meakins Christie Labs, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
airway remodeling; airway smooth muscle; asthma; cell-cell interaction; T cell; NECROSIS-FACTOR-ALPHA; NF-KAPPA-B; LEUKEMIA INHIBITORY FACTOR; MESSENGER-RNA EXPRESSION; EPIDERMAL-GROWTH-FACTOR; TNF-ALPHA; SIGNALING PATHWAYS; VCAM-1; EXPRESSION; OX40; LIGAND; IFN-GAMMA;
D O I
10.1152/ajplung.00121.2024
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Cross talk between T cells and airway smooth muscle (ASM) may play a role in modulating asthmatic airway inflammation and remodeling. Infiltrating T cells have been observed within the ASM bundles of asthmatics, and a wide range of direct and indirect interactions between T cells and ASM has been demonstrated using various in vitro and in vivo model systems. Contact-dependent mechanisms such as ligation and activation of cellular adhesion and costimulatory molecules, as well as the formation of lymphocyte-derived membrane conduits, facilitate the adhesion, bidirectional communication, and transfer of materials between T and ASM cells. T cell-derived cytokines, particularly of the Th1, Th2, and Th17 subsets, modulate the secretome, proliferation, and contractility of ASM cells. This review summarizes the mechanisms governing T cell-ASM cross talk in the context of asthma. Understanding the underlying mechanistic basis is important for directing future research and developing therapeutic interventions targeted toward this complex interaction.
引用
收藏
页码:L382 / L394
页数:13
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