Gordon J, Ley S C, Melamed M D, Aman P, Hughes-Jones N C
J Exp Med. 1984 May 1;159(5):1554-9. doi: 10.1084/jem.159.5.1554.
B lymphoblasts immortalized by the Epstein-Barr virus (EBV) exhibit autocrine growth stimulation--that is they release a soluble activity to which they respond by growth. A minimally supplemented serum-free medium conditioned by lymphoblastoid cells in their log phase of growth (LCL-CM) was found to contain autostimulatory activity allowing us to explore the mechanism of autocrine growth for these cell-types in defined conditions. Below cell densities capable of supporting autonomous growth, continued proliferation in serum-free medium was dependent on both added LCL-CM and transferrin. Neither activity alone was capable of sustaining growth. At higher cell densities, transferrin by itself was sufficient to maintain the autocrine loop. The action of the autostimulatory factor appeared to reside in its ability to prime cells continually for a proliferative response to transferrin by enhancing the expression of transferrin receptors at the lymphoblast surfaces. The implications of these findings for normal B cell physiology and their possible relation to oncogenesis are discussed.
由爱泼斯坦-巴尔病毒(EBV)永生化的B淋巴母细胞表现出自分泌生长刺激——也就是说,它们释放一种可溶性活性物质,并对其作出生长反应。发现由处于对数生长期的淋巴母细胞条件化的最低限度补充的无血清培养基(LCL-CM)含有自刺激活性,这使我们能够在确定的条件下探索这些细胞类型的自分泌生长机制。在低于能够支持自主生长的细胞密度时,无血清培养基中的持续增殖依赖于添加的LCL-CM和转铁蛋白。单独任何一种活性都不能维持生长。在较高细胞密度时,转铁蛋白自身就足以维持自分泌循环。自刺激因子的作用似乎在于其能够通过增强淋巴母细胞表面转铁蛋白受体的表达,持续使细胞对转铁蛋白产生增殖反应做好准备。讨论了这些发现对正常B细胞生理学的意义及其与肿瘤发生的可能关系。