Suppr超能文献

小鼠肺对青石棉的反应。2. 长期接触长纤维后的肺纤维化

Response of mouse lung to crocidolite asbestos. 2. Pulmonary fibrosis after long fibres.

作者信息

Adamson I Y, Bowden D H

出版信息

J Pathol. 1987 Jun;152(2):109-17. doi: 10.1002/path.1711520207.

Abstract

To determine the cellular and fibrogenic responses of the lung to long asbestos fibres, mice were instilled intratracheally with 0.1 mg of a sample of long crocidolite fibres. Animals were killed at intervals to 20 weeks with 3H thymidine injected one h before death. Following bronchoalveolar lavage, an increase in polymorph neutrophils (PMN) and alveolar macrophages (AM) was found during the first week, accompanied by elevated glucosaminidase and alveolar protein levels. Although the PMN number dropped, some were always recovered by lavage to 20 weeks. Early multifocal necrosis of bronchiolar epithelium was followed by a large increase in labelling of epithelial cells and underlying fibroblasts. Epithelial overgrowth of luminal long fibres and inflammatory exudates was followed by giant cell and granuloma formation in the interstitium. After four weeks collagen levels were significantly increased and fibrosis was seen in these peribronchiolar locations. A few small fibres were observed in AM but no evidence of fibrosis was seen in alveolar walls. These findings suggest that injury to bronchial and bronchiolar epithelium allows long fibres to reach the interstitium where subsequent macrophage-fibroblast interactions result in a severe fibrotic reaction that resembles the bronchiolar component of human asbestosis.

摘要

为了确定肺部对长石棉纤维的细胞和纤维化反应,给小鼠气管内注入0.1毫克长青石棉纤维样本。在处死动物前1小时注射3H胸腺嘧啶核苷,间隔一定时间至20周处死动物。支气管肺泡灌洗后发现,第一周多形核中性粒细胞(PMN)和肺泡巨噬细胞(AM)增加,同时氨基葡萄糖苷酶和肺泡蛋白水平升高。虽然PMN数量下降,但通过灌洗在20周时总能回收一些。细支气管上皮早期多灶性坏死之后,上皮细胞和其下的成纤维细胞标记大量增加。腔内长纤维和炎性渗出物的上皮过度生长之后,间质中出现巨细胞和肉芽肿形成。四周后,胶原水平显著增加,在这些细支气管周围部位可见纤维化。在AM中观察到一些小纤维,但肺泡壁未见纤维化证据。这些发现表明,支气管和细支气管上皮损伤使长纤维到达间质,随后巨噬细胞-成纤维细胞相互作用导致严重的纤维化反应,类似于人类石棉沉着病的细支气管成分。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验