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Determination of Energy Charge Potential in the C6 Glioma and the HepG-2 Cell Culture

机译:C6脑胶质瘤和HepG-2细胞培养物中能量电荷潜能的确定

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摘要

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.
机译:能量电荷电势(ECP)是5'-三磷酸腺苷(ATP),-二磷酸酯(ADP)和-一磷酸酯(AMP)之间的比率;它反映了生物系统中的高能键含量。在正常的生理条件下,ECP的值介于0.7和1.0之间。在这项研究中,使用两种不同的方法提取腺苷核苷酸(ATP,ADP和AMP),以确定C6胶质瘤和HepG-2人肝癌细胞系中的ECP。在第一种方法中,通过胰蛋白酶消化将细胞从培养板中去除,然后使用高氯酸提取核苷酸。一些胰蛋白酶消化的细胞用于细胞计数,从而允许计算每个细胞的平均核苷酸水平。在第二种方法中,在除去培养基后立即将高氯酸直接加入到培养板中。该方法导致任何可能降解核苷酸并改变其在细胞中水平的酶促过程的立即终止。腺苷核苷酸通过高效液相色谱法测定。直接提取方法产生的总腺苷核苷酸(TAN)水平比胰蛋白酶消化后获得的总腺苷核苷酸水平高出两倍以上。对于C6胶质瘤细胞,在胰蛋白酶消化后提取细胞时,TAN池中ATP / ADP / AMP的比例为0.70:0.15:0.15,而细胞为0.36:0.27:0.37。同样,对于HepG-2细胞,直接提取后的比例为0.62:0.15:0.23,而胰蛋白酶消化后的比例为0.15:0.28:0.57。使用直接提取方法的结果,C6胶质瘤细胞的细胞ECP值为0.78±0.06,HepG-2细胞的细胞ECP值为0.70±0.06。与使用胰蛋白酶消化方法获得的ECP值相比(分别为0.50±0.05和0.29±0.12),直接提取方法得出的ECP值在两种细胞系中均显着更高,表明正常,健康细胞的能量状态。

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