Vajner Ludek, Vytásek Richard, Lachmanová Vera, Uhlík Jirí, Konrádová Václava, Novotná Jana, Hampl Václav, Herget Jan
Department of Histology and Embryology, Charles University, Prague.
Int J Exp Pathol. 2006 Oct;87(5):383-91. doi: 10.1111/j.1365-2613.2006.00493.x.
Chronic hypoxia results in pulmonary hypertension due to vasoconstriction and structural remodelling of peripheral lung blood vessels. We hypothesize that vascular remodelling is initiated in the walls of prealveolar pulmonary arteries by collagenolytic metalloproteinases (MMP) released from activated mast cells. Distribution of mast cells and their expression of interstitial collagenase, MMP-13, in lung conduit, small muscular, and prealveolar arteries was determined quantitatively in rats exposed for 4 and 20 days to hypoxia as well as after 7-day recovery from 20-day hypoxia (10% O2). Mast cells were identified using Toluidine Blue staining, and MMP-13 expression was detected using monoclonal antibody. After 4, but not after 20 days of hypoxia, a significant increase in the number of mast cells and their MMP-13 expression was found within walls of prealveolar arteries. In rats exposed for 20 days, MMP-13 positive mast cells accumulated within the walls of conduit arteries and subpleurally. In recovered rats, MMP-13 positive mast cells gathered at the prealveolar arterial level as well as in the walls of small muscular arteries; these mast cells stayed also in the conduit part of the pulmonary vasculature. These data support the hypothesis that perivascular pulmonary mast cells contribute to the vascular remodelling in hypoxic pulmonary hypertension in rats by releasing interstitial collagenase.
慢性缺氧会因外周肺血管的血管收缩和结构重塑而导致肺动脉高压。我们推测,血管重塑是由活化肥大细胞释放的胶原溶解金属蛋白酶(MMP)在肺泡前肺动脉壁中引发的。对暴露于缺氧环境4天和20天的大鼠以及从20天缺氧(10%氧气)恢复7天后的大鼠,定量测定肥大细胞在肺导管、小肌性动脉和肺泡前动脉中的分布及其间质胶原酶MMP-13的表达。使用甲苯胺蓝染色鉴定肥大细胞,使用单克隆抗体检测MMP-13的表达。缺氧4天后,但20天后未发现,肺泡前动脉壁内肥大细胞数量及其MMP-13表达显著增加。在暴露20天的大鼠中,MMP-13阳性肥大细胞在导管动脉壁内和胸膜下积聚。在恢复的大鼠中,MMP-13阳性肥大细胞聚集在肺泡前动脉水平以及小肌性动脉壁内;这些肥大细胞也留在肺血管的导管部分。这些数据支持这样的假说,即血管周围肺肥大细胞通过释放间质胶原酶促成大鼠缺氧性肺动脉高压中的血管重塑。