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二氧化硅释放的巨噬细胞因子对体外结缔组织中蛋白质合成的影响。

Effect of SiO2-liberated macrophage factor on protein synthesis in connective tissue in vitro.

作者信息

Aalto M, Turakainen H, Kulonen E

出版信息

Scand J Clin Lab Invest. 1979 May;39(3):205-13. doi: 10.1080/00365517909106095.

Abstract
  1. To elucidate the role of macrophages in fibrosis the effect of the SiO2-liberated macrophage factor was assessed on protein synthesis in granulation-tissue slices. SiO2 could be replaced by chrysotile asbestos. The active factor is found in the 45/55% sucrose interface of macrophage homogenate. 2. There is no evidence of the involvement of collagenase. 3. The SiO2 effect is not influenced by the addition of yeast RNA to the incubation medium. 4. At a small concentration of polyvinylpyridine-N-oxide (PVNO) protein synthesis in the granulation tissue slices is stimulated, but at higher concentrations PVNO prevented the liberation of the fibrogenic factor from macrophages by SiO2. 5. Phospholipase C and trypsin inhibited the effect of SiO2, which was partially abolished also by heating, and by repeated freezing and thawing. 6. The macrophage RNAse, its inhibitors and fibroblast mRNA are suggested as key factors in the development of fibrosis.
摘要
  1. 为阐明巨噬细胞在纤维化中的作用,评估了二氧化硅释放的巨噬细胞因子对肉芽组织切片中蛋白质合成的影响。二氧化硅可用温石棉替代。活性因子存在于巨噬细胞匀浆的45/55%蔗糖界面中。2. 没有证据表明胶原酶参与其中。3. 向孵育培养基中添加酵母RNA不会影响二氧化硅的作用。4. 在低浓度的聚乙烯吡啶-N-氧化物(PVNO)作用下,肉芽组织切片中的蛋白质合成受到刺激,但在高浓度时,PVNO可阻止二氧化硅从巨噬细胞中释放致纤维化因子。5. 磷脂酶C和胰蛋白酶可抑制二氧化硅的作用,加热、反复冻融也可部分消除该作用。6. 巨噬细胞核糖核酸酶、其抑制剂和成纤维细胞信使核糖核酸被认为是纤维化发展的关键因素。

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