Airway smooth muscle in airway reactivity and remodeling: what have we learned?

被引:184
作者
Prakash, Y. S. [1 ,2 ]
机构
[1] Mayo Clin, Dept Anesthesiol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Physiol & Biomed Engn, Rochester, MN 55905 USA
关键词
lung; asthma; inflammation; calcium; bronchoconstriction; bronchodilation; proliferation; extracellular matrix; development; PROTEIN-COUPLED RECEPTORS; GROWTH-FACTOR RECEPTOR; OPERATED CA2+ ENTRY; NF-KAPPA-B; EXTRACELLULAR-MATRIX PRODUCTION; THYMIC STROMAL LYMPHOPOIETIN; CAVEOLIN-1 KNOCKOUT MICE; INDUCED CD38 EXPRESSION; CENTRAL-NERVOUS-SYSTEM; TNF-ALPHA;
D O I
10.1152/ajplung.00259.2013
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
It is now established that airway smooth muscle (ASM) has roles in determining airway structure and function, well beyond that as the major contractile element. Indeed, changes in ASM function are central to the manifestation of allergic, inflammatory, and fibrotic airway diseases in both children and adults, as well as to airway responses to local and environmental exposures. Emerging evidence points to novel signaling mechanisms within ASM cells of different species that serve to control diverse features, including 1) [Ca2+](i) contractility and relaxation, 2) cell proliferation and apoptosis, 3) production and modulation of extracellular components, and 4) release of pro- vs. anti-inflammatory mediators and factors that regulate immunity as well as the function of other airway cell types, such as epithelium, fibroblasts, and nerves. These diverse effects of ASM "activity" result in modulation of bronchoconstriction vs. bronchodilation relevant to airway hyperresponsiveness, airway thickening, and fibrosis that influence compliance. This perspective highlights recent discoveries that reveal the central role of ASM in this regard and helps set the stage for future research toward understanding the pathways regulating ASM and, in turn, the influence of ASM on airway structure and function. Such exploration is key to development of novel therapeutic strategies that influence the pathophysiology of diseases such as asthma, chronic obstructive pulmonary disease, and pulmonary fibrosis.
引用
收藏
页码:L912 / L933
页数:22
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