Hibbs M S, Postlethwaite A E, Mainardi C L, Seyer J M, Kang A H
J Exp Med. 1983 Jan 1;157(1):47-59. doi: 10.1084/jem.157.1.47.
The cell-cell interactions between fibroblasts and mononuclear leukocytes (MNL) which promote alterations in collagen accumulation were examined using a system of co-culture of human fibroblasts and peripheral blood MNL. The stimulation of collagen production was optimal after 48 h of co-culture and the increase in collagen correlated directly with the number of MNL added. The enhancement of collagen production was seen in both autologous and allogeneic co-cultures. Stimulation of non-collagenous protein was also noted. Co-culture supernatants contained soluble substances that were capable of stimulating collagen production, although they stimulated collagen production to a lesser degree than direct co-culture. Fractionation of these supernatants on Sephadex G-200 revealed a predominant area of stimulatory activity at 160,000 mol wt. Lesser areas of activity were noted at molecular weights of 80,000 and 25,000. Determination of the types of collagen produced by fibroblasts during co-culture with MNL showed that the ratio of type I:III collagen was decreased. These alterations in both the quantitative and qualitative accumulation of collagen mimic the changes often seen in wound healing and early inflammation suggesting that cellular interactions between fibroblasts and MNL may be important in the modulation of collagen production in normal and pathologic states.
利用人成纤维细胞和外周血单核白细胞(MNL)共培养系统,研究了促进胶原蛋白积累变化的成纤维细胞与单核白细胞(MNL)之间的细胞间相互作用。共培养48小时后,胶原蛋白生成的刺激效果最佳,且胶原蛋白的增加与添加的MNL数量直接相关。自体和异体共培养中均可见胶原蛋白生成增强。还注意到非胶原蛋白的刺激作用。共培养上清液含有能够刺激胶原蛋白生成的可溶性物质,尽管它们刺激胶原蛋白生成的程度低于直接共培养。在Sephadex G - 200上对这些上清液进行分级分离,发现在分子量160,000处有一个主要的刺激活性区域。在分子量80,000和25,000处也注意到较小的活性区域。对与MNL共培养期间成纤维细胞产生的胶原蛋白类型的测定表明,I型:III型胶原蛋白的比例降低。胶原蛋白在数量和质量积累上的这些变化模拟了伤口愈合和早期炎症中常见的变化,表明成纤维细胞与MNL之间的细胞相互作用可能在正常和病理状态下胶原蛋白生成的调节中起重要作用。