Smith G L
J Cell Biol. 1977 Jun;73(3):761-7. doi: 10.1083/jcb.73.3.761.
Multiplication-stimulating activity (MSA), a protein which stimulates DNA synthesis and growth of chicken embryo fibroblasts, was purified from serum-free medium conditioned by the growth of a rat liver cell line. Purified MSA was shown to rapidly stimulate ouabain-sensitive Na+, K+-ATPase activity as measured by both enzyme assay and rate of 86Rubidium uptake. Labeled ouabain binding was also shown to increase after stimulation of quiescent cells by serum or purified MSA. Conditions which interfere with the ability of the cells to accumulate potassium, such as the presence of the specific inhibitor, ouabain; incubation in potassium-free medium; or the presence of the potassium ionophore, valinomycin, were all demonstrated to inhibit the stimulation of DNA synthesis by serum or purified MSA. These results suggest that an early event in the stimulation of DNA synthesis by purified MSA is an activation of membrane Na+, K+-ATPase with a resulting accumulation of potassium ions inside the cell.
增殖刺激活性(MSA)是一种能刺激鸡胚成纤维细胞DNA合成和生长的蛋白质,它是从一种大鼠肝细胞系生长所条件化的无血清培养基中纯化得到的。通过酶活性测定和铷-86摄取率测定均表明,纯化的MSA能快速刺激哇巴因敏感的Na⁺、K⁺-ATP酶活性。在用血清或纯化的MSA刺激静止细胞后,标记的哇巴因结合也显示增加。干扰细胞积累钾能力的条件,如存在特异性抑制剂哇巴因、在无钾培养基中孵育或存在钾离子载体缬氨霉素,均被证明可抑制血清或纯化的MSA对DNA合成的刺激作用。这些结果表明,纯化的MSA刺激DNA合成的早期事件是膜Na⁺、K⁺-ATP酶的激活,导致钾离子在细胞内积累。