Department of Biology, Hong Kong Baptist University, Kowloon, Hong Kong.
Toxicol Mech Methods. 2003;13(2):97-101. doi: 10.1080/15376510309843.
The energy charge potential (ECP) is the ratio among adenosine 5'-triphosphate (ATP), -diphosphate (ADP), and -monophosphate (AMP); it reflects the high-energy-bond content in biological systems. Under normal physiological conditions, the value of ECP is between 0.7 and 1.0. In this study, two different methods were used to extract adenosine nucleotides (ATP, ADP, and AMP) for determination of the ECP in the C6 glioma and the HepG-2 human hepatoma cell lines. In the first method, cells were removed from culture plates by trypsinization before the nucleotides were extracted using perchloric acid. Some of the trypsinized cells were used for a cell count, thereby allowing the calculation of an average nucleotide level per cell. In the second method, perchloric acid was added directly to the culture plate immediately after the medium was removed. This method resulted in an instant termination of any enzymatic process that might degrade the nucleotides and alter their levels in cells. Adenosine nucleotides were determined by high-performance liquid chromatography. The direct extraction method yielded a total adenosine nucleotide (TAN) level more than twofold higher than that obtained following trypsinization. For the C6 glioma cells, the ratio of ATP to ADP to AMP in the TAN pool was 0.70:0.15:0.15, as compared to 0.36:0.27:0.37 when cells were extracted following trypsinization. Similarly, for the HepG-2 cells, the ratio was 0.62:0.15:0.23 following direct extraction, as compared to 0.15:0.28:0.57 following trypsinization. Using the results from the direct extraction method, the value of the cellular ECP was 0.78 +/- 0.06 for the C6 glioma cells and 0.70 +/- 0.06 for the HepG-2 cells. Compared to the ECP values obtained using the trypsinization method (0.50 +/- 0.05 and 0.29 +/- 0.12, respectively), the ECP values derived using the direct extraction method were significantly greater in both cell lines and were suggestive of the energy status of normal, healthy cells.
能量荷电位 (ECP) 是三磷酸腺苷 (ATP)、二磷酸腺苷 (ADP) 和一磷酸腺苷 (AMP) 之间的比率;它反映了生物系统中的高能键含量。在正常生理条件下,ECP 的值在 0.7 到 1.0 之间。在这项研究中,使用两种不同的方法从 C6 神经胶质瘤和 HepG-2 人肝癌细胞系中提取腺嘌呤核苷酸 (ATP、ADP 和 AMP) 以测定 ECP。在第一种方法中,用胰蛋白酶消化细胞从培养板中除去细胞,然后用高氯酸提取核苷酸。部分用胰蛋白酶消化的细胞用于细胞计数,从而可以计算每个细胞的平均核苷酸水平。在第二种方法中,在去除培养基后立即将高氯酸直接添加到培养板中。这种方法立即终止任何可能降解核苷酸并改变细胞内核苷酸水平的酶促过程。通过高效液相色谱法测定腺嘌呤核苷酸。直接提取法得到的总腺嘌呤核苷酸 (TAN) 水平比胰蛋白酶消化后得到的水平高出两倍以上。对于 C6 神经胶质瘤细胞,TAN 池中的 ATP 与 ADP 与 AMP 的比值为 0.70:0.15:0.15,而胰蛋白酶消化后为 0.36:0.27:0.37。同样,对于 HepG-2 细胞,直接提取后比值为 0.62:0.15:0.23,而胰蛋白酶消化后为 0.15:0.28:0.57。使用直接提取方法的结果,C6 神经胶质瘤细胞的细胞 ECP 值为 0.78 +/- 0.06,HepG-2 细胞为 0.70 +/- 0.06。与胰蛋白酶消化法得到的 ECP 值 (分别为 0.50 +/- 0.05 和 0.29 +/- 0.12) 相比,两种细胞系中直接提取法得到的 ECP 值均显著更高,表明正常健康细胞的能量状态。