EAGLE H, PIEZ K
J Exp Med. 1962 Jul 1;116(1):29-43. doi: 10.1084/jem.116.1.29.
At least seven compounds synthesized by cultured cells in amounts which should suffice for sustained growth have nevertheless proved under certain conditions necessary for survival (asparagine, cystine, glutamine, homocystine inositol, pyruvate, serine). In every instance so far examined, that requirement has been population-dependent, disappearing at cell densities sufficiently large to bring the concentration in the medium and in the cellular pool to metabolically effective levels before the cells died of the specific deficiency. At population densities of less than 100 cells per ml, serine was required by all cultured cells so far studied. With more exigent strains, such as the RT6 strain of rabbit fibroblast and the P388 mouse leukemia, the serine requirement disappeared only at populations in excess of 50,000 and 150,000 cells per ml, respectively. The requirement for pyruvate by the latter cell as an alternative to serine also disappeared at that population density. In a cystine-free medium there were population-dependent requirements for cystine, homocystine, or serine, depending on the experimental conditions. With methionine and glucose as cystine precursors, the critical population density permitting cellular survival and growth was in excess of 200,000 cells/ml. The provision of homocystine as an intermediate reduced the critical population density to 10,000 to 60,000 cells/ml; with the further provision of serine, the critical cell concentration permitting growth was reduced to 50 to 500 cells/ml. Cells adapted to glutamic acid, and capable of utilizing it as a substitute for glutamine, nevertheless required exogeneous glutamine at cellular densities of less than 50,000 cells per ml. In some experiments, the provision of asparagine reduced the critical population density to 10,000 cells/ml, presumably because of its glutamine-sparing action. Inositol is required by most cell lines, despite their demonstrated capacity to synthesize it from glucose. With at least one cell line (HeLa), sustained growth was occasionally achieved in an inositol-free medium if the population density was maintained in excess of 240,000 cells/ml. The possible implications of these findings with respect to the loss of specific organ functions in dispersed cell culture are discussed.
由培养细胞合成的至少七种化合物,其合成量应足以维持生长,但在某些生存所需条件下(天冬酰胺、胱氨酸、谷氨酰胺、高胱氨酸、肌醇、丙酮酸、丝氨酸)却被证明是必需的。在迄今为止所研究的每一个实例中,这种需求都取决于细胞群体数量,当细胞密度足够大,使得培养基和细胞内池中这些物质的浓度在细胞因特定缺乏而死亡之前达到代谢有效水平时,这种需求就会消失。在每毫升低于100个细胞的群体密度下,迄今为止所研究的所有培养细胞都需要丝氨酸。对于更苛求的细胞株,如兔成纤维细胞的RT6株和P388小鼠白血病细胞株,丝氨酸需求分别仅在每毫升超过50,000个和150,000个细胞的群体数量时才消失。后一种细胞对丙酮酸作为丝氨酸替代品的需求在该群体密度时也消失了。在无胱氨酸培养基中,根据实验条件,对胱氨酸、高胱氨酸或丝氨酸存在群体依赖性需求。以蛋氨酸和葡萄糖作为胱氨酸前体时,允许细胞存活和生长的临界群体密度超过每毫升200,000个细胞。提供高胱氨酸作为中间产物可将临界群体密度降低至每毫升10,000至60,000个细胞;进一步提供丝氨酸后,允许生长的临界细胞浓度降低至每毫升50至500个细胞。适应谷氨酸并能够将其用作谷氨酰胺替代品的细胞,在每毫升低于50,000个细胞的群体密度时仍需要外源谷氨酰胺。在一些实验中,提供天冬酰胺可将临界群体密度降低至每毫升10,000个细胞,推测是由于其节省谷氨酰胺的作用。大多数细胞系都需要肌醇,尽管它们已被证明有能力从葡萄糖合成肌醇。对于至少一种细胞系(HeLa),如果群体密度维持在每毫升超过240,000个细胞,偶尔也能在无肌醇培养基中实现持续生长。本文讨论了这些发现对于分散细胞培养中特定器官功能丧失的可能意义。