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Altered functions of alveolar macrophages and NK cells involved in asbestos-related diseases

机译:参与石棉相关疾病的肺泡巨噬细胞和NK细胞功能改变

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摘要

Asbestos exposure causes asbestosis and malignant mesothelioma, disorders which remain difficult to cure. We focused on alveolar macrophages (AM) and natural killer (NK) cells in asbestosis and mesothelioma, respectively, and examined their functions upon exposure to asbestos or in patients with mesothelioma. Exposure to asbestos caused rat AM to exhibit high production of transforming growth factor-beta (TGF-β) with prolonged survival in the absence of other cells, not simultaneously with the apoptosis caused by asbestos. The NK cell line showed impaired cytotoxicity with altered expression of activating receptors upon exposure to asbestos, and primary NK cells in culture with asbestos and peripheral blood NK cells in mesothelioma shared a decrease in expression of NKp46, a representative activating receptor. The AM finding indicates that AM contribute to asbestosis by playing a direct role in the fibrogenic response, as well as the inflammatory response. The response of NK cells indicates that exposure to asbestos has an immune-suppressive effect, as well as a tumorigenic effect. Our studies therefore reveal novel effects of asbestos exposure on AM and tumor immunity, which may represent valuable information for construction of a strategy for prevention and cure of asbestosis and malignant mesothelioma.
机译:接触石棉会导致石棉沉着和恶性间皮瘤,这些疾病仍然难以治愈。我们分别研究了石棉沉滞症和间皮瘤中的肺泡巨噬细胞(AM)和自然杀伤(NK)细胞,并在接触石棉或间皮瘤患者后检查了它们的功能。暴露于石棉会导致大鼠AM在不存在其他细胞的情况下表现出高产量的转化生长因子-β(TGF-β),并具有延长的存活时间,而不是与石棉引起的细胞凋亡同时发生。 NK细胞系暴露于石棉后,细胞毒性减弱,活化受体表达改变,间皮瘤中与石棉和外周血NK细胞培养的原代NK细胞共享代表性的活化受体NKp46的表达降低。 AM的发现表明AM通过在纤维化反应以及炎症反应中发挥直接作用来促进石棉沉着症。 NK细胞的反应表明,接触石棉具有免疫抑制作用以及致瘤作用。因此,我们的研究揭示了石棉暴露对AM和肿瘤免疫的新影响,这可能为构建预防和治疗石棉沉滞症和恶性间皮瘤的策略提供有价值的信息。

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