Deng Linhong, Fairbank Nigel J, Cole Darren J, Fredberg Jeffrey J, Maksym Geoffrey N
Physiology Program, Dept. of Environmental Health, Harvard School of Public Health, Boston, MA 02115, USA.
J Appl Physiol (1985). 2005 Aug;99(2):634-41. doi: 10.1152/japplphysiol.00025.2005. Epub 2005 Apr 21.
The application of mechanical stresses to the airway smooth muscle (ASM) cell causes time-dependent cytoskeletal stiffening and remodeling (Deng L, Fairbank NJ, Fabry B, Smith PG, and Maksym GN. Am J Physiol Cell Physiol 287: C440-C448, 2004). We investigated here the extent to which these behaviors are modulated by the state of cell activation (tone). Localized mechanical stress was applied to the ASM cell in culture via oscillating beads (4.5 mum) that were tightly bound to the actin cytoskeleton (CSK). Tone was reduced from baseline level using a panel of relaxant agonists (10(-3) M dibutyryl cAMP, 10(-4) M forskolin, or 10(-6) M formoterol). To assess functional changes, we measured cell stiffness (G') using optical magnetic twisting cytometry, and to assess structural changes of the CSK we measured actin accumulation in the neighborhood of the bead. Applied mechanical stress caused a twofold increase in G' at 120 min. After cessation of applied stress, G' diminished only 24 +/- 6% (mean +/- SE) at 1 h, leaving substantial residual effects that were largely irreversible. However, applied stress-induced stiffening could be prevented by ablation of tone. Ablation of tone also inhibited the amount of actin accumulation induced by applied mechanical stress (P < 0.05). Thus the greater the contractile tone, the greater was applied stress-induced CSK stiffening and remodeling. As regards pathobiology of asthma, this suggests a maladaptive positive feedback in which tone potentiates ASM remodeling and stiffening that further increases stress and possibly leads to worsening airway function.
对气道平滑肌(ASM)细胞施加机械应力会导致细胞骨架随时间变硬和重塑(邓L、费尔班克NJ、法布里B、史密斯PG和马克西姆GN。《美国生理学杂志:细胞生理学》287卷:C440 - C448页,2004年)。我们在此研究了这些行为在多大程度上受细胞激活状态(张力)的调节。通过紧密结合肌动蛋白细胞骨架(CSK)的振荡微珠(4.5微米)对培养的ASM细胞施加局部机械应力。使用一组舒张激动剂(10⁻³ M二丁酰环磷腺苷、10⁻⁴ M福斯可林或10⁻⁶ M福莫特罗)将张力从基线水平降低。为了评估功能变化,我们使用光磁扭转细胞术测量细胞硬度(G'),为了评估CSK的结构变化,我们测量微珠附近的肌动蛋白积累。施加机械应力在120分钟时使G'增加了两倍。施加应力停止后,1小时时G'仅降低24±6%(平均值±标准误),留下大量基本不可逆的残余效应。然而,通过消除张力可以防止施加应力诱导的变硬。消除张力也抑制了施加机械应力诱导的肌动蛋白积累量(P < 0.05)。因此,收缩张力越大,施加应力诱导的CSK变硬和重塑就越明显。就哮喘的病理生物学而言,这表明存在一种适应不良的正反馈,即张力增强ASM重塑和变硬,进而进一步增加应力并可能导致气道功能恶化。