Grinnell F, Feld M K
Cell. 1979 May;17(1):117-29. doi: 10.1016/0092-8674(79)90300-3.
Experiments were carried out to test the hypothesis that the initial attachment and spreading of human fibroblasts in serum-free medium occurs to cell fibronectin which has been secretd spread on tissue culture substrata in serum-free medium in 60 min. When potential protein adsorption sites on the substratum were covered with bovine serum albumin before initial human fibroblasts attachment, their subsequent attachment to the substratum was prevented. When substratum adsorption sites were covered immediately after initial attachment, subsequent cell spreading was prevented. The distribution of fibronectin on human fibroblast surfaces during initial attachment and spreading was studied by indirect immunofluorescence analysis using a monospecific anti-cold-insoluble globulin antiserum. The initial appearance (10 min) of fibronectin was in spots over the entire cell surface. Concomitant with human fibroblast spreading, the random distribution of sites disappeared, and most fibronectin was subsequently observed in spots at the cell substratum interface (60 min). A fibrillar pattern of fibronectin appeared later (2-8 hr). The sites beneath the cells could be visualized as footprints on the substratum following treatment of the attached human fibroblasts with 0.1 M NaOH. A second fluorescence pattern of fibronectin secreted on the substratum was characterized by a diffuse halo around the cells and a very faint, diffuse staining elsewhere on the substratum. Another cell type (baby hamster kideny cells) was used to assay biologically for the presence or absence of the factor secreted by human fibroblasts on the substratum. Human fibroblasts were found to secrete an adhesion factor for baby hamster kidney cells into the substratum in a time- and temperature-dependent fashion, and immunological studies indicated that the factor secreted by human fibroblasts was cross-reactive with cold-in-soluble globulin, the plasma form of fibronectin. The conditioning factor secreted by the human fibroblasts was also found to be an attachment and spreading factor for human fibroblasts in experiments measuring human fibroblast adhesion to fibronectin footprints of human fibroblasts. Substratum-adsorbed cold-insoluble globulin was also found to be an attachment and spreading factor for human fibroblasts. Based upon the timing of appearance of conditioning factors on the substratum and the immunofluorescence patterns, it seems that the diffusely organized fibronectin on the substratum constitutes the sites to which cell attachment occurs. The bright spots of fibronectin that appear beneath the cells may represent fibronectin reorganization during cell spreading.
人成纤维细胞在无血清培养基中的初始附着和铺展发生于细胞纤连蛋白,该蛋白在无血清培养基中于60分钟内分泌并铺展在组织培养底物上。当在人成纤维细胞初始附着前用牛血清白蛋白覆盖底物上的潜在蛋白质吸附位点时,其随后对底物的附着被阻止。当在初始附着后立即覆盖底物吸附位点时,随后的细胞铺展被阻止。使用单特异性抗冷不溶性球蛋白抗血清通过间接免疫荧光分析研究了初始附着和铺展过程中人成纤维细胞表面纤连蛋白的分布。纤连蛋白的初始出现(10分钟)呈现在整个细胞表面的斑点中。与人成纤维细胞铺展同时,位点的随机分布消失,随后在细胞-底物界面的斑点中观察到大多数纤连蛋白(60分钟)。纤连蛋白的纤维状模式稍后出现(2 - 8小时)。在用0.1 M NaOH处理附着的人成纤维细胞后,细胞下方的位点可在底物上可视化为足迹。底物上分泌的纤连蛋白的另一种荧光模式的特征是细胞周围有弥散的光晕,底物其他部位有非常微弱的弥散染色。使用另一种细胞类型(幼仓鼠肾细胞)从生物学角度检测底物上是否存在人成纤维细胞分泌的因子。发现人成纤维细胞以时间和温度依赖性方式向底物中分泌一种针对幼仓鼠肾细胞的黏附因子,并且免疫学研究表明人成纤维细胞分泌的因子与冷不溶性球蛋白(纤连蛋白的血浆形式)有交叉反应。在测量人成纤维细胞对人成纤维细胞纤连蛋白足迹的黏附的实验中,还发现人成纤维细胞分泌的调节因子也是人成纤维细胞的附着和铺展因子。底物吸附的冷不溶性球蛋白也被发现是人成纤维细胞的附着和铺展因子。基于调节因子在底物上出现的时间和免疫荧光模式,似乎底物上弥散组织的纤连蛋白构成了细胞附着发生的位点。细胞下方出现的纤连蛋白亮点可能代表细胞铺展过程中纤连蛋白的重新组织。