Harada J J, Porter C W, Morris D R
J Cell Physiol. 1981 Jun;107(3):413-26. doi: 10.1002/jcp.1041070313.
Chinese hamster ovary (CHO) cells in culture were limited for polyamines through the use of alpha-methylornithine (alpha MO), a competitive inhibitor of ornithine decarboxylase. Initial exposure of the cells to the inhibitor caused growth rate and intracellular polyamine content to decline continuously. Reseeding the alpha MO-treated cells into medium containing the inhibitor resulted in steady-state (exponential) growth at cell densities below 5 x 10(3) cells/cm2, at a rate approximately twofold slower than untreated cells. Under these conditions, putrescine and spermidine were undetectable and spermine remained relatively constant at a level approximately half that found in untreated cells. Addition of exogenous putrescine elevated the polyamine content and stimulated the growth of alpha MO-treated cultures. Thus, growth rate correlated with polyamine content in the alpha MO-treated cells. The growth of reseeded, alpha MO-treated cells became nonexponential at a density (5 x 10(3) cells/cm2) far below that at which untreated cells departed from exponential growth (1 x 10(5) cells/cm2). Medium obtained from high density, alpha MO-treated cultures inhibited the growth of cells at low density in the presence of alpha MO. Doubling the concentration of the defined components of conditioned medium did not markedly affect its capacity to inhibit growth. However, dialysis completely not markedly affect its capacity to inhibit growth. However, dialysis completely removed the inhibitory activity from conditioned medium. The results imply that a low molecular weight inhibitor of growth is produced by polyamine-limited cells. This is a variable that must be controlled in studies with polyamine-limited animal cells. Morphological studies indicated that subcellular organelles, including mitochondria, were largely unaffected by treatment with alpha MO. The maintenance of mitochondrial integrity in the presence of alpha MO demonstrates that the swelling of mitochondria observed previously in cells treated with methylglyoxal bis(guanylhydrazone) was not due to polyamine limitation. alpha MO-treated cells did, however, accumulate numerous cytoplasmic vacuoles. The identity of these vacuoles and their relationship to cellular physiology is not yet understood.
通过使用鸟氨酸脱羧酶的竞争性抑制剂α-甲基鸟氨酸(αMO),使培养中的中国仓鼠卵巢(CHO)细胞的多胺受到限制。细胞最初暴露于该抑制剂会导致生长速率和细胞内多胺含量持续下降。将经αMO处理的细胞重新接种到含有该抑制剂的培养基中,在细胞密度低于5×10³个细胞/cm²时会出现稳态(指数)生长,其速率比未处理的细胞慢约两倍。在这些条件下,腐胺和亚精胺无法检测到,精胺保持相对恒定,其水平约为未处理细胞中发现水平的一半。添加外源性腐胺可提高多胺含量并刺激经αMO处理的培养物生长。因此,在经αMO处理的细胞中,生长速率与多胺含量相关。重新接种的、经αMO处理的细胞在密度(5×10³个细胞/cm²)远低于未处理细胞偏离指数生长的密度(1×10⁵个细胞/cm²)时,其生长变得不再呈指数增长。从高密度、经αMO处理的培养物中获得的培养基在存在αMO的情况下会抑制低密度细胞的生长。将条件培养基中特定成分的浓度加倍并不会显著影响其抑制生长的能力。然而,透析完全消除了条件培养基中的抑制活性。结果表明,多胺受限的细胞会产生一种低分子量的生长抑制剂。这是在多胺受限的动物细胞研究中必须控制的一个变量。形态学研究表明,包括线粒体在内的亚细胞器在很大程度上不受αMO处理的影响。在存在αMO的情况下线粒体完整性的维持表明,先前在用甲基乙二醛双(胍基腙)处理的细胞中观察到的线粒体肿胀并非由于多胺限制。然而,经αMO处理的细胞确实积累了大量细胞质空泡。这些空泡的身份及其与细胞生理学的关系尚不清楚。