Guidry C, McFarland R J, Morris R, Witherspoon C D, Hook M
Department of Biochemistry, University of Alabama, Birmingham 35294.
Invest Ophthalmol Vis Sci. 1992 Jul;33(8):2429-35.
The capacities of porcine choroidal fibroblasts, retinal glial cells, and retinal pigment epithelial cells to contract collagen gels in vitro were compared. Experiments with varied cell numbers indicated that glial cells are the most effective, followed by choroidal fibroblasts and retinal pigment epithelial cells. Analysis of the secretory products from cultures of these cell types revealed that retinal pigment epithelial cells synthesize and secrete peptides that promote fibroblast contraction of collagen gels in vitro. The mechanism of action of the retinal pigment epithelial cell-secreted contraction promoter was compared with that found in serum (type A) and secreted by cultured endothelial cells (type B). Like the serum factor, the retinal pigment epithelial cell-secreted factor was not dependent on active protein synthesis by the target cell and must be present continuously to promote contraction.
比较了猪脉络膜成纤维细胞、视网膜神经胶质细胞和视网膜色素上皮细胞在体外收缩胶原凝胶的能力。不同细胞数量的实验表明,神经胶质细胞最为有效,其次是脉络膜成纤维细胞和视网膜色素上皮细胞。对这些细胞类型培养物分泌产物的分析显示,视网膜色素上皮细胞合成并分泌能促进胶原凝胶在体外成纤维细胞收缩的肽。将视网膜色素上皮细胞分泌的收缩促进剂的作用机制与血清中发现的(A型)和培养的内皮细胞分泌的(B型)进行了比较。与血清因子一样,视网膜色素上皮细胞分泌的因子不依赖于靶细胞的活性蛋白质合成,并且必须持续存在才能促进收缩。