Viallard V, Denis C, Trocheris V, Murat J C
Int J Biochem. 1986;18(3):263-9. doi: 10.1016/0020-711x(86)90116-3.
Effect of glutamine deprivation (GLN- medium) and of its replacement by 4mM ammonium chloride (GLN-/NH4+ medium) or by 4mM glutamate (GLN-/Gt+ medium) was studied on growth rate, morphology and metabolism of HT29 human colon cancer cells. Growth rates were modified as follows: at the first passage, growth of GLN- cells was strongly decreased (doubling time: 192 hr vs 32 hr in control cells grown in GLN+ medium); GLN-/NH4+ cells and GLN-/Gt+ cells were found to have doubling times of 72 and 70 hr, respectively. At the 8th passage, doubling times were decreased in all cases, being: 144 hr for GLN- cells, 60 hr for GLN-/NH4+ cells and 24 hr for GLN-/Gt+ cells, which indicates a capacity of adaptation of the cell-line to new culture conditions. GLN- cells and GLN-/NH4+ cells were found to exhibit an enterocytic type of differentiation (polarization of the cell layer with apical and cystic brush border and tight junctions); GLN-/Gt+ cells remained undifferentiated and comparable to control GLN+ cells. Glycogen level varied according to the phases of the culture, with a trend to lower level in glutamine deprived cells; glucose uptake and lactate production varied as a function of the medium composition and of the phases of the culture. At the 8th passage, all the glutamine deprived cells produced less lactate than control; GLN-/Gt+ cells were found to utilize less glucose than others.
研究了谷氨酰胺缺乏(GLN-培养基)以及用4mM氯化铵(GLN-/NH4+培养基)或4mM谷氨酸(GLN-/Gt+培养基)替代谷氨酰胺对HT29人结肠癌细胞生长速率、形态和代谢的影响。生长速率变化如下:在首次传代时,GLN-细胞的生长显著降低(倍增时间:192小时,而在GLN+培养基中生长的对照细胞为32小时);发现GLN-/NH4+细胞和GLN-/Gt+细胞的倍增时间分别为72小时和70小时。在第8次传代时,所有情况下的倍增时间均缩短,GLN-细胞为144小时,GLN-/NH4+细胞为60小时,GLN-/Gt+细胞为24小时,这表明细胞系有适应新培养条件的能力。发现GLN-细胞和GLN-/NH4+细胞表现出肠细胞样分化(细胞层极化,有顶端和囊状刷状缘以及紧密连接);GLN-/Gt+细胞仍未分化,与对照GLN+细胞相似。糖原水平根据培养阶段而变化,谷氨酰胺缺乏的细胞有降低的趋势;葡萄糖摄取和乳酸产生随培养基组成和培养阶段而变化。在第8次传代时,所有谷氨酰胺缺乏的细胞产生的乳酸都比对照少;发现GLN-/Gt+细胞比其他细胞利用的葡萄糖少。