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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.
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页码:L382 / L394
页数:13
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