Maksym Geoffrey N, Deng Linhong, Fairbank Nigel J, Lall C A, Connolly Sarah C
School of Biomedical Engineering, Dalhousie University, Halifax, NS B3H 1W2, Canada.
Can J Physiol Pharmacol. 2005 Oct;83(10):913-22. doi: 10.1139/y05-091.
Airway smooth muscle (ASM) cells are constantly under mechanical strain as the lung cyclically expands and deflates, and this stretch is now known to modulate the contractile function of ASM. However, depending on the experimental conditions, stretch is either beneficial or harmful limiting or enhancing contractile force generation, respectively. Stretch caused by a deep inspiration is known to be beneficial in limiting or reversing airway constriction in healthy individuals, and oscillatory stretch lowers contractile force and stiffness or lengthens muscle in excised airway tissue strips. Stretch in ASM culture has generally been reported to cause increased contractile function through increases in proliferation, contractile protein content, and organization of the cell cytoskeleton. Recent evidence indicates the type of stretch is critically important. Growing cells on flexible membranes where stretch is non-uniform and anisotropic leads to pro-contractile changes, whereas uniform biaxial stretch causes the opposite effects. Furthermore, the role of contractile tone might be important in modulating the response to mechanical stretch in cultured cells. This report will review the contrasting evidence for modulation of contractile function of ASM, both in vivo and in vitro, and summarize the recent evidence that mechanical stress applied either acutely within 2 h or chronically over 11 d is a potent stimulus for cytoskeletal remodelling and stiffening. We will also point to new data suggesting that perhaps some of the difference in response to stretch might lie with one of the fundamental differences in the ASM environment in asthma and in culture--the presence of elevated contractile tone.
气道平滑肌(ASM)细胞在肺部周期性扩张和收缩时不断受到机械应变,现在已知这种拉伸可调节ASM的收缩功能。然而,根据实验条件的不同,拉伸要么有益,要么有害,分别限制或增强收缩力的产生。已知深吸气引起的拉伸有利于限制或逆转健康个体的气道收缩,而振荡拉伸会降低收缩力和硬度,或使离体气道组织条中的肌肉变长。一般报道称,ASM培养中的拉伸通过增加增殖、收缩蛋白含量和细胞骨架的组织来导致收缩功能增强。最近的证据表明,拉伸的类型至关重要。在柔性膜上培养细胞,拉伸不均匀且各向异性会导致促收缩变化,而均匀双轴拉伸则会产生相反的效果。此外,收缩张力在调节培养细胞对机械拉伸的反应中可能起重要作用。本报告将综述体内和体外调节ASM收缩功能的对比证据,并总结最近的证据,即急性(2小时内)或慢性(超过11天)施加的机械应力是细胞骨架重塑和硬化的有力刺激因素。我们还将指出新的数据,表明对拉伸反应的一些差异可能在于哮喘和培养环境中ASM环境的一个根本差异——收缩张力升高。