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基质金属蛋白酶-2 参与肺动脉高压肉鸡肺小动脉中膜肥厚。

Involvement of matrix metalloproteinase-2 in medial hypertrophy of pulmonary arterioles in broiler chickens with pulmonary arterial hypertension.

机构信息

Key Laboratory of Animal Virology of Ministry of Agriculture, College of Animal Sciences, Zhejiang University, Hangzhou, China.

出版信息

Vet J. 2012 Aug;193(2):420-5. doi: 10.1016/j.tvjl.2012.01.017. Epub 2012 Feb 28.

DOI:10.1016/j.tvjl.2012.01.017
PMID:22377328
Abstract

Medial hypertrophy of pulmonary arterioles during pulmonary arterial hypertension (PAH) in humans is associated with enhanced proliferation of smooth muscle cells (SMCs). Elevated matrix metalloproteinase (MMP)-2 has been found in pulmonary artery SMCs (PA-SMCs) in humans with idiopathic PAH, leading to the hypothesis that MMP-2 contributes to the proliferation and migration of vascular SMCs in the pathogenesis of PAH. Rapidly growing meat-type (broiler) chickens provide a model of spontaneous PAH. The present study was conducted to determine whether MMP-2 is involved in the medial hypertrophy of pulmonary arterioles in this model. Cultured PA-SMCs from normal birds were used to evaluate the effect of MMPs on cell proliferation. Gelatin zymography showed that endothelin (ET)-1-induced proliferation of PA-SMCs was concomitant with increased pro- and active MMP-2 production. Reverse transcription PCR demonstrated upregulation of MMP-2 mRNA. However, PA-SMC proliferation was inhibited by the MMP inhibitors doxycycline and cis-9-octadecenoyl-N-hydroxylamide. In vivo experiments revealed a significant increase of MMP-2 expression in hypertrophied pulmonary arterioles of PAH broiler chickens, which was positively correlated with wall thickness and medial hypertrophy. MMP-2 may contribute to medial hypertrophy in pulmonary arterioles during PAH in broiler chickens by enhancing the proliferation of vascular SMCs.

摘要

肺动脉高压(PAH)患者的肺小动脉中层发生肥厚,与平滑肌细胞(SMCs)增殖增强有关。在特发性 PAH 患者的肺动脉 SMC(PA-SMC)中发现基质金属蛋白酶(MMP)-2 升高,导致 MMP-2 有助于 PAH 发病机制中血管 SMC 的增殖和迁移的假说。快速生长的肉用型(肉鸡)鸡提供了自发性 PAH 的模型。本研究旨在确定 MMP-2 是否参与该模型中小肺动脉中层的肥厚。从正常鸟类培养的 PA-SMC 用于评估 MMP 对细胞增殖的影响。明胶酶谱显示内皮素(ET)-1 诱导的 PA-SMC 增殖伴随着前体和活性 MMP-2 产生的增加。逆转录 PCR 显示 MMP-2 mRNA 的上调。然而,MMP 抑制剂强力霉素和顺-9-十八碳烯酰-N-羟基酰胺抑制了 PA-SMC 的增殖。体内实验显示 PAH 肉鸡肥厚性肺小动脉中 MMP-2 表达显著增加,与壁厚度和中层肥厚呈正相关。MMP-2 通过增强血管 SMC 的增殖可能有助于肉鸡 PAH 时的小动脉中层肥厚。

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