石棉暴露增强羊肺泡巨噬细胞释放成纤维细胞生长因子。

I Lemaire, M Rola-Pleszczynski, R Bégin
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摘要

在绵羊石棉肺模型中研究了自由气道细胞(FAC)与肺成纤维细胞之间的相互作用。三组每组6只羊分别经气管内反复灌注生理盐水(对照组)、328 mg(低剂量)和2282 mg(高剂量)UICC温石棉B石棉。第一次灌胃16个月后,对各组羊进行段性支气管肺泡灌洗(BAL)获得的FAC进行不同时间间隔的孵育,并测定其培养上清(FAC- sn)对人胚胎肺成纤维细胞增殖的影响。对照动物的facc - sn刺激肺成纤维细胞加入胸腺嘧啶(3H-TdR)的数量是未处理培养的2 - 3倍。最大刺激发生在48小时,与72小时成纤维细胞数量的显著增加相关。对照羊的FAC群体主要由巨噬细胞(79%)和淋巴细胞(15%)组成,这两个细胞群体的分离表明只有巨噬细胞产生刺激成纤维细胞的活性。在孵育1小时内产生,在2至4小时之间达到最大值。这种活性在56摄氏度下不透析性和30分钟的稳定性,但在80摄氏度和低ph下被破坏。此外,暴露于石棉的绵羊的facc - sn刺激成纤维细胞将3H-TdR掺入5至6倍,而对照组的facc - sn则是2至3倍。这种活性可能调节纤维形成,并可能参与最终的石棉纤维形成反应。
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Asbestos exposure enhances the release of fibroblast growth factor by sheep alveolar macrophages.

Interaction between free airway cells (FAC) and lung fibroblasts was studied in a sheep model of asbestosis. Three groups of six sheep each received, respectively, by repeated intratracheal instillations, saline (control), 328 mg (low dose), and 2282 mg (high dose) of UICC chrysotile B asbestos. Sixteen months after the first instillation, FAC obtained by segmental bronchoalveolar lavage (BAL) of sheep in each group were incubated for various intervals, and the effect of their culture supernatants (FAC-SN) on human embryonic lung fibroblast proliferation was determined. FAC-SN from control animals stimulated thymidine (3H-TdR) incorporation by lung fibroblasts two- to threefold compared to untreated cultures. Maximal stimulation was observed at 48 hr and was correlated with a significant increase of the fibroblast population at 72 hr. FAC population from control sheep consisted primarily of macrophages (79%) and lymphocytes (15%), and separation of these two cell populations indicated that only macrophages produced the fibroblast-stimulating activity. Production occurred within 1 hr of incubation and was maximal between 2 and 4 hr. This activity was nondialyzable and stable at 56 degrees C for 30 min, but was destroyed at 80 degrees C and low pH. Moreover, FAC-SN from sheep exposed to asbestos stimulated 3H-TdR incorporation by fibroblasts five- to sixfold compared to two- to threefold for control FAC-SN. This activity may modulate fibrogenesis and may be involved in the eventual fibrogenic response to asbestos.

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