Zamaraeva Maria V, Sabirov Ravshan Z, Manabe Ken-ichi, Okada Yasunobu
Department of Cell Physiology, National Institute for Physiological Sciences, Okazaki 444-8585, Japan.
Biochem Biophys Res Commun. 2007 Nov 23;363(3):687-93. doi: 10.1016/j.bbrc.2007.09.019. Epub 2007 Sep 18.
It was previously shown that cells die with increased cytosolic ATP after stimulation with apoptotic inducers including staurosporine (STS). To identify the source of apoptotic ATP elevation, we monitored, in real time, the cytosolic ATP level in luciferase-expressing HeLa cells. A mitochondrial uncoupler or a respiration chain inhibitor was found to decrease cytosolic ATP by about 50%. However, even when mitochondrial ATP synthesis was suppressed, STS induced a profound elevation of intracellular ATP. In contrast, the STS-induced ATP increase was prevented by any of three inhibitors of the glycolytic pathway: 2-deoxyglucose, iodoacetamide, and NaF. The STS effect strongly depended on intracellular calcium and was mimicked by a calcium ionophore. We conclude that Ca(2+)-dependent activation of anaerobic glycolysis, but not aerobic mitochondrial oxidative phosphorylation, is responsible for the STS-induced elevation of ATP in apoptotic HeLa cells.
先前的研究表明,在用包括星形孢菌素(STS)在内的凋亡诱导剂刺激后,细胞会伴随着胞质ATP的增加而死亡。为了确定凋亡时ATP升高的来源,我们实时监测了表达荧光素酶的HeLa细胞中的胞质ATP水平。发现线粒体解偶联剂或呼吸链抑制剂可使胞质ATP降低约50%。然而,即使线粒体ATP合成受到抑制,STS仍能引起细胞内ATP的显著升高。相反,糖酵解途径的三种抑制剂(2-脱氧葡萄糖、碘乙酰胺和氟化钠)中的任何一种都能阻止STS诱导的ATP增加。STS的作用强烈依赖于细胞内钙,并且可被钙离子载体模拟。我们得出结论,在凋亡的HeLa细胞中,Ca(2+)依赖的无氧糖酵解激活而非有氧线粒体氧化磷酸化,是导致STS诱导的ATP升高的原因。