Rydell-Törmänen Kristina, Johnson Jill R, Fattouh Ramzi, Jordana Manel, Erjefält Jonas S
Department of Experimental Medical Science, Division of Vascular and Airway Research, BMC D12, S-22184 Lund, Sweden.
Am J Respir Cell Mol Biol. 2008 Jul;39(1):61-7. doi: 10.1165/rcmb.2007-0441OC. Epub 2008 Feb 28.
Structural changes to the lung are associated with chronic asthma. In addition to alterations to the airway wall, asthma is associated with vascular modifications, although this aspect of remodeling is poorly understood. We sought to evaluate the character and kinetics of vascular remodeling in response to chronic aeroallergen exposure. Because many ovalbumin-driven models used to investigate allergic airway disease do so in the absence of persistent airway inflammation, we used a protocol of chronic respiratory exposure to house dust mite extract (HDME), which has been shown to induce persistent airway inflammation consistent with that seen in humans with asthma. Mice were exposed to HDME intranasally for 7 or 20 consecutive weeks, and resolution of the inflammatory and remodeling response to allergen was investigated 4 weeks after the end of a 7-week exposure protocol. Measures of vascular remodeling, including total collagen deposition, procollagen I production, endothelial and smooth muscle cell proliferation, smooth muscle area, and presence of myofibroblasts, were investigated histologically in lung vessels of different sizes and locations. We observed an increase in total collagen content, which did not resolve upon cessation of allergen exposure. Other parameters were significantly increased after 7 and/or 20 weeks of allergen exposure but returned to baseline after allergen withdrawal. We conclude that respiratory HDME exposure induces airway remodeling and pulmonary vascular remodeling, and, in accordance with airway remodeling, some components of these structural changes may be irreversible.
肺部结构变化与慢性哮喘相关。除气道壁改变外,哮喘还与血管改变有关,尽管对这种重塑方面的了解甚少。我们试图评估慢性吸入变应原暴露后血管重塑的特征和动力学。由于许多用于研究过敏性气道疾病的卵清蛋白驱动模型是在没有持续性气道炎症的情况下进行的,我们采用了一种慢性呼吸道暴露于屋尘螨提取物(HDME)的方案,该方案已被证明可诱导与哮喘患者所见一致的持续性气道炎症。将小鼠连续7周或20周经鼻暴露于HDME,并在7周暴露方案结束后4周研究对变应原的炎症和重塑反应的消退情况。通过组织学方法研究不同大小和位置的肺血管中血管重塑的指标,包括总胶原沉积、I型前胶原产生、内皮细胞和平滑肌细胞增殖、平滑肌面积以及肌成纤维细胞的存在情况。我们观察到总胶原含量增加,在变应原暴露停止后并未消退。其他参数在变应原暴露7周和/或20周后显著增加,但在变应原撤除后恢复到基线水平。我们得出结论,呼吸道暴露于HDME可诱导气道重塑和肺血管重塑,并且与气道重塑一致,这些结构变化的某些成分可能是不可逆的。