Gysin R, Moore B W, Proffitt R T, Deuel T F, Caldwell K, Glaser L
J Biol Chem. 1980 Feb 25;255(4):1515-20.
The influence of serum on the synthesis of the nervous system specific S-100 protein has been investigated in the rat glial cell clone C61a. In sparse cells, where S-100 synthesis is low, removal of serum leads to a 2- to 3-fold increase of the rate of S-100 synthesis relative to total soluble cell protein. Measurements of S-100 content by radioimmunoassay showed that sparse cells are accumulating S-100 much more rapidly in the absence of serum. Our findings suggest that serum components inhibit the expression of S-100 synthesis in sparse cells by a concentration-dependent mechanism. This effect does not correlate directly with the reduced cellular growth rate in low serum or serum-free medium. Lipid-free medium, which has little growth-promoting activity, maintains the capacity to lower the rate of S-100 synthesis. A partially purified extract of platelets can substitute for serum in repressing the synthesis of the S-100 protein.
在大鼠神经胶质细胞克隆C61a中,研究了血清对神经系统特异性S-100蛋白合成的影响。在S-100合成较低的稀疏细胞中,去除血清会导致S-100合成速率相对于总可溶性细胞蛋白增加2至3倍。通过放射免疫测定法测量S-100含量表明,在无血清的情况下,稀疏细胞积累S-100的速度要快得多。我们的研究结果表明,血清成分通过浓度依赖性机制抑制稀疏细胞中S-100合成的表达。这种作用与低血清或无血清培养基中细胞生长速率降低没有直接关联。几乎没有生长促进活性的无脂培养基,仍保持降低S-100合成速率的能力。血小板的部分纯化提取物可以替代血清来抑制S-100蛋白的合成。