Schwartz E, Bienkowski R S, Coltoff-Schiller B, Goldfischer S, Blumenfeld O O
J Cell Biol. 1982 Feb;92(2):462-70. doi: 10.1083/jcb.92.2.462.
Culture conditions can modify the composition of the extracellular matrix of cultured calf aortas smooth muscle cells. In the absence of ascorbate the major components of the matrix are microfibrillar proteins; deposition of collagen occurs upon ascorbate supplementation and, with increased time of exposure of cells to ascorbate, collagen becomes the dominant protein of the extracellular matrix (greater than 80%). Collagen accumulation follows a sigmoidal time-course, suggesting that it is a cooperative phenomenon. Covalent crosslinks are not required for collagen accumulation in the matrix. Microfibrillar proteins and increased amounts of proteoglycans and fibronectin accumulate concurrently with collagen but elastin deposition was not observed either with or without ascorbate feeding. Addition of ascorbate leads to a general stimulation of incorporation of [14C]proline into cellular protein and to changes in cell growth parameters and morphology: cell-doubling time decreases from 62 to 47 h and plating efficiency increases approximately fourfold. We conclude that the composition of the extracellular matrix assembled by cultured cells is subject to experimental manipulation and that changes in endogenously deposited matrix may have significant effects on cellular functions.
培养条件可改变培养的小牛主动脉平滑肌细胞的细胞外基质组成。在缺乏抗坏血酸的情况下,基质的主要成分是微原纤维蛋白;补充抗坏血酸后会发生胶原蛋白沉积,并且随着细胞暴露于抗坏血酸的时间增加,胶原蛋白成为细胞外基质的主要蛋白质(超过80%)。胶原蛋白的积累遵循S形时间进程,表明这是一种协同现象。基质中胶原蛋白的积累不需要共价交联。微原纤维蛋白以及蛋白聚糖和纤连蛋白含量的增加与胶原蛋白同时积累,但无论是否添加抗坏血酸,均未观察到弹性蛋白沉积。添加抗坏血酸会普遍刺激[14C]脯氨酸掺入细胞蛋白,并导致细胞生长参数和形态发生变化:细胞倍增时间从62小时降至47小时,接种效率提高约四倍。我们得出结论,培养细胞组装的细胞外基质组成可通过实验操作进行调控,内源性沉积基质的变化可能对细胞功能产生重大影响。