Kajstura J, Michalik M, Zaporowska-Siwiak E, Korohoda W
Department of Cell Biology, Jan Zurzycki Institute of Molecular Biology, Jagellonian University, Kraków, Poland.
Folia Histochem Cytobiol. 1988;26(2):83-9.
Ehrlich ascites tumour (EAT) cells were cultured in vitro in Eagle's MEM and Medium 199 with a lowered amino-acid content. Under these conditions EAT cells lose their rounded shape typical of highly malignant cancer cells, and begin to spread on the substratum. The changes in EAT cell morphology are preceded by a decrease in the rate of protein synthesis. These changes were maintained for three days after returning the cells to Eagle's MEM with a normal amino-acid content, but the return to control media did not cause reasumption of growth in the once spread cells. The increase in glucose content (up to five-fold) or the presence of inhibitors of DNA synthesis did not prevent the attachment and flattening of EAT cells in media with a lowered amino acid content. Several possible mechanisms of the influence of restricted amino-acid availability on the changes in EAT cell surface properties are pointed out and the need for study of cancer cell responses to restricted nutrition is discussed.
艾氏腹水瘤(EAT)细胞在氨基酸含量降低的Eagle's MEM培养基和199培养基中进行体外培养。在这些条件下,EAT细胞失去了高度恶性癌细胞典型的圆形形态,并开始在培养基上扩散。EAT细胞形态的变化之前,蛋白质合成速率会降低。将细胞放回氨基酸含量正常的Eagle's MEM培养基后,这些变化持续了三天,但回到对照培养基中并没有使曾经扩散的细胞恢复生长。葡萄糖含量的增加(高达五倍)或DNA合成抑制剂的存在并不能阻止EAT细胞在氨基酸含量降低的培养基中附着和平展。指出了限制氨基酸供应对EAT细胞表面特性变化影响的几种可能机制,并讨论了研究癌细胞对营养限制反应的必要性。