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体外缺氧增加分离的大鼠肺肥大细胞中基质金属蛋白酶和类胰蛋白酶的产生。

In vitro hypoxia increases production of matrix metalloproteinases and tryptase in isolated rat lung mast cells.

作者信息

Maxová H, Novotná J, Vajner L, Tomášová H, Vytásek R, Vízek M, Bačáková L, Valoušková V, Eliášová T, Herget J

机构信息

Department of Pathological Physiology, Second Medical School, Charles University, Prague, Czech Republic.

出版信息

Physiol Res. 2008;57(6):903-910. doi: 10.33549/physiolres.931278. Epub 2007 Nov 30.

Abstract

Chronic hypoxia results in hypoxic pulmonary hypertension characterized by fibrotization and muscularization of the walls of peripheral pulmonary arteries. This vessel remodeling is accompanied by an increase in the amount of lung mast cells (LMC) and the presence of small collagen cleavage products in the vessel walls. We hypothesize that hypoxia activates LMC, which release matrix metalloproteinases (MMPs) cleaving collagen and starting increased turnover of connective tissue proteins. This study was designed to determine whether in vitro hypoxia stimulates production of MMPs in rat LMC and increases their collagenolytic activity. The LMC were separated on the Percoll gradient and then were divided into two groups and cultivated for 24 h in 21 % O(2) + 5 % CO(2) or in 10 % O(2) + 5 % CO(2). Presence of the rat interstitial tissue collagenase (MMP-13) in LMC was visualized by immunohistological staining and confirmed by Western blot analysis. Total MMPs activity and tryptase activity were measured in both cultivation media and cellular extracts. Exposure to hypoxia in vitro increased the amount of cells positively labeled by anti-MMP-13 antibody as well as activities of all measured enzymes. The results therefore support the concept that LMC are an important source of increased collagenolytic activity in chronic hypoxia.

摘要

慢性缺氧会导致缺氧性肺动脉高压,其特征为外周肺动脉壁纤维化和肌化。这种血管重塑伴随着肺肥大细胞(LMC)数量的增加以及血管壁中存在小的胶原蛋白裂解产物。我们推测,缺氧会激活LMC,LMC释放基质金属蛋白酶(MMPs),裂解胶原蛋白并启动结缔组织蛋白周转增加。本研究旨在确定体外缺氧是否刺激大鼠LMC中MMPs的产生并增加其胶原olytic活性。LMC在Percoll梯度上分离,然后分为两组,在21% O₂ + 5% CO₂或10% O₂ + 5% CO₂中培养24小时。通过免疫组织化学染色观察LMC中大鼠间质组织胶原酶(MMP-13)的存在,并通过蛋白质印迹分析进行确认。在两种培养基和细胞提取物中测量总MMPs活性和类胰蛋白酶活性。体外暴露于缺氧增加了抗MMP-13抗体阳性标记的细胞数量以及所有测量酶的活性。因此,结果支持LMC是慢性缺氧中胶原olytic活性增加的重要来源这一概念。

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