Kelleher J K, Bryan B M, Mallet R T, Holleran A L, Murphy A N, Fiskum G
Department of Physiology, George Washington University School of Medicine and Health Sciences, Washington, DC 20037.
Biochem J. 1987 Sep 15;246(3):633-9. doi: 10.1042/bj2460633.
The CO2-ratios method is applied to the analysis of abnormalities of TCA (tricarboxylic acid)-cycle metabolism in AS-30D rat ascites-hepatoma cells. This method utilizes steady-state 14CO2-production rates from pairs of tracers of the same compound to evaluate TCA-cycle flux patterns. Equations are presented that quantitatively convert CO2 ratios into estimates of probability of flux through TCA-cycle-related pathways. Results of this study indicated that the ratio of 14CO2 produced from [1,4-14C]succinate to 14CO2 produced from [2,3-14C]succinate was increased by the addition of glutamine (5 mM) to the medium. An increase in the succinate CO2 ratio is quantitatively related to an increased flux of unlabelled carbon into the TCA-cycle-intermediate pools. Analysis of 14C distribution in [14C]citrate derived from [2,3-14C]succinate indicated that flux from the TCA cycle to the acetyl-CoA-derived carbons of citrate was insignificant. Thus the increased succinate CO2 ratio observed in the presence of glutamine could only result from an increased flux of carbon into the span of the TCA cycle from citrate to oxaloacetate. This result is consistent with increased flux of glutamine to alpha-oxoglutarate in the incubation medium containing exogenous glutamine. Comparison of the pyruvate CO2 ratio, steady-state 14CO2 production from [2-14C]pyruvate versus [3-14C]pyruvate, with the succinate 14CO2 ratio detected flux of pyruvate to C4 TCA-cycle intermediates in the medium containing glutamine. This result was consistent with the observation that [14C]aspartate derived from [2-14C]pyruvate was labelled in C-2 and C-3. 14C analysis also produced evidence for flux of TCA-cycle carbon to alanine. This study demonstrates that the CO2-ratios method is applicable in the analysis of the metabolic properties of AS-30D cells. This methodology has verified that the atypical TCA-cycle metabolism previously described for AS-30D-cell mitochondria occurs in intact AS-30D rat hepatoma cells.
二氧化碳比率法被应用于分析AS - 30D大鼠腹水肝癌细胞中三羧酸(TCA)循环代谢的异常情况。该方法利用同一化合物的一对示踪剂的稳态14CO2生成速率来评估TCA循环通量模式。文中给出了将二氧化碳比率定量转化为通过TCA循环相关途径通量概率估计值的方程式。本研究结果表明,向培养基中添加谷氨酰胺(5 mM)会使[1,4 - 14C]琥珀酸产生的14CO2与[2,3 - 14C]琥珀酸产生的14CO2的比率增加。琥珀酸二氧化碳比率的增加与未标记碳进入TCA循环中间产物池的通量增加在数量上相关。对源自[2,3 - 14C]琥珀酸的[14C]柠檬酸中14C分布的分析表明,从TCA循环到柠檬酸中乙酰辅酶A衍生碳的通量微不足道。因此,在谷氨酰胺存在下观察到的琥珀酸二氧化碳比率增加只能是由于从柠檬酸到草酰乙酸的TCA循环跨度内碳通量增加所致。这一结果与在含有外源性谷氨酰胺的孵育培养基中谷氨酰胺向α - 酮戊二酸的通量增加相一致。将丙酮酸二氧化碳比率,即[2 - 14C]丙酮酸与[3 - 14C]丙酮酸的稳态14CO2生成量,与琥珀酸14CO2比率进行比较,检测到了丙酮酸在含有谷氨酰胺的培养基中向C4 TCA循环中间产物的通量。这一结果与观察到的源自[2 - 14C]丙酮酸的[14C]天冬氨酸在C - 2和C - 3处被标记相一致。14C分析还为TCA循环碳向丙氨酸的通量提供了证据。本研究表明,二氧化碳比率法适用于分析AS - 30D细胞的代谢特性。该方法已证实,先前描述的AS - 30D细胞线粒体的非典型TCA循环代谢发生在完整的AS - 30D大鼠肝癌细胞中。