Reiser K M, Last J A
Toxicology. 1979 May;13(1):51-72.
Although the pulmonary and extrapulmonary manifestations of silicosis in humans have been extensively documented, the mechanisms by which the fibrogenic effects of silica are manifested remain obscure. In this review, both in vitro and in vivo models of silicosis are discussed, with emphasis on the potential methodological pitfalls of each. In animal models, for example, species variability, silica type and route of administration all effect the results obtained. Tissue culture work has provided evidence that the fibroblast-macrophage interaction is a key event in fibrogenesis. However, critical variables in experimental design make it difficult to compare the often conflicting results of different workers. Experimental conditions that directly affect collagen chain biosynthesis and subsequent hydroxylation of proline appear to be of particular importance. It is concluded that, in part because of methodological difficulties, there are insufficient data to draw firm conclusions regarding the effect of silica-exposed macrophages on collagen biosynthesis by fibroblasts in vitro; there are few, if any, data concerning the role of the macrophage that has ingested silica in human or animal models of silicosis.
虽然矽肺在人体中的肺部和肺外表现已有大量文献记载,但二氧化硅致纤维化作用的表现机制仍不清楚。在这篇综述中,讨论了矽肺的体外和体内模型,重点关注每种模型潜在的方法学缺陷。例如,在动物模型中,物种差异、二氧化硅类型和给药途径都会影响所得结果。组织培养研究提供了证据,表明成纤维细胞 - 巨噬细胞相互作用是纤维化形成中的关键事件。然而,实验设计中的关键变量使得难以比较不同研究者常常相互矛盾的结果。直接影响胶原链生物合成以及随后脯氨酸羟化的实验条件似乎尤为重要。得出的结论是,部分由于方法学上的困难,没有足够的数据就体外二氧化硅暴露的巨噬细胞对成纤维细胞胶原生物合成的影响得出确凿结论;在人类或动物矽肺模型中,关于吞噬了二氧化硅的巨噬细胞的作用,几乎没有(如果有的话)数据。