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隐源性机化性肺炎:肺泡巨噬细胞中白细胞介素-8和纤连蛋白基因表达增加。

Cryptogenic organizing pneumonia: increased expression of interleukin-8 and fibronectin genes by alveolar macrophages.

作者信息

Carré P C, King T E, Mortensen R, Riches D W

机构信息

Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.

出版信息

Am J Respir Cell Mol Biol. 1994 Jan;10(1):100-5. doi: 10.1165/ajrcmb.10.1.8292374.

Abstract

Cryptogenic organizing pneumonia (COP) is a fibrotic process that primarily involves the alveolar spaces, alveolar ducts, and small conducting airways. The pathogenesis is not understood. Recent histopathologic studies have shown that during the cellular phase of COP, fibronectin deposits are present in the lung. Moreover, a neutrophil alveolitis is frequently seen in COP. Little is known about the involvement of alveolar macrophages in the pathogenesis of COP. However, alveolar macrophages are the principal resident cells in the airways, and they are thought to play a central role in the fibrotic process by virtue of their ability to express and release cytokines such as interleukin-8 (IL-8; a neutrophil chemotactic factor) and fibronectin (FN; a fibrogenic matrix-associated protein). We have quantified the spontaneous gene expression of IL-8 and FN by alveolar macrophages from five nonsmoking individuals with COP and compared them with 10 normal, healthy volunteers (five smokers, five nonsmokers). Expression of IL-8 and FN was measured by a quantitative assay employing reverse transcription of mRNA and the polymerase chain reaction. beta-actin mRNA expression was quantified as an internal standard, and the expression of FN and IL-8 transcripts was calculated as a ratio with beta-actin. The mean +/- SEM of the IL-8/beta-actin ratio in alveolar macrophages from patients with COP was 0.45 +/- 0.07, which was significantly higher than the level from either normal smokers (0.19 +/- 0.02, P = 0.008) or normal nonsmokers (0.16 +/- 0.01, P = 0.005).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

隐源性机化性肺炎(COP)是一种主要累及肺泡腔、肺泡管和小传导气道的纤维化过程。其发病机制尚不清楚。最近的组织病理学研究表明,在COP的细胞阶段,肺内存在纤连蛋白沉积。此外,COP中常可见中性粒细胞肺泡炎。关于肺泡巨噬细胞在COP发病机制中的作用知之甚少。然而,肺泡巨噬细胞是气道中的主要驻留细胞,它们被认为凭借其表达和释放细胞因子如白细胞介素-8(IL-8;一种中性粒细胞趋化因子)和纤连蛋白(FN;一种与纤维化基质相关的蛋白)的能力在纤维化过程中发挥核心作用。我们对5名非吸烟COP患者的肺泡巨噬细胞中IL-8和FN的自发基因表达进行了定量,并将其与10名正常健康志愿者(5名吸烟者,5名非吸烟者)进行比较。IL-8和FN的表达通过采用mRNA逆转录和聚合酶链反应的定量测定法进行测量。β-肌动蛋白mRNA表达作为内标进行定量,FN和IL-8转录本的表达以与β-肌动蛋白的比值计算。COP患者肺泡巨噬细胞中IL-8/β-肌动蛋白比值的平均值±标准误为0.45±0.07,显著高于正常吸烟者(0.19±0.02,P = 0.008)或正常非吸烟者(0.16±0.01,P = 0.005)。(摘要截断于250字)

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