Graduate Institute of Technology, University of Arkansas at Little Rock, 2801 S. University Ave., Little Rock, AR 72204, USA.
Mol Cell Biochem. 2010 Dec;345(1-2):61-8. doi: 10.1007/s11010-010-0560-0. Epub 2010 Aug 20.
Accumulations of higher inositol polyphosphates, diphosphoinositol polyphosphates or pyrophosphates, have been implicated to mediate cellular apoptosis. Whether cellular levels of lower inositol phosphates (lower than inositol hexakisphosphates) change during apoptosis is not known, although these inositol phosphates are known to play crucial roles in a number of cellular signaling processes including calcium mobilization. Therefore, in this study, we have examined changes in cellular levels of inositol phosphates following metabolic labeling of these compounds by [(3)H]myo-inositol and induction of apoptosis. The levels of inositol mono- and bis-phosphates were increased, whereas the levels of inositol tris- and tetrakis-phosphates decreased significantly with an increasing rate of apoptosis induced by etoposide in a dose-dependent manner. NaF treatment, which increased the rate of apoptosis in a time- and dose-dependent manner, also increased the levels of inositol mono- and bis-phosphates and drastically reduced the levels of inositol tris- and tetrakis-phosphates. Prior treatment with antimycin A, a strategy used to reverse the NaF-induced accumulations of higher InsPs, partially reduced the effects of NaF on apoptosis as well as the levels of lower InsPs. Taken together, our results suggest that cellular levels of lower InsPs are altered during apoptosis.
细胞内低磷酸肌醇(低于肌醇六磷酸)的水平在细胞凋亡过程中是否发生变化尚不清楚,尽管这些肌醇磷酸在包括钙动员在内的许多细胞信号转导过程中起着至关重要的作用。因此,在这项研究中,我们通过用 [(3)H]肌醇对这些化合物进行代谢标记,并诱导细胞凋亡,研究了细胞内肌醇磷酸水平的变化。结果发现,随着依托泊苷诱导细胞凋亡的速率增加,肌醇单磷酸和双磷酸的水平增加,而肌醇三磷酸和四磷酸的水平显著降低,呈剂量依赖性。氟化物处理(NaF)以时间和剂量依赖的方式增加细胞凋亡的速率,同时也增加了肌醇单磷酸和双磷酸的水平,并极大地降低了肌醇三磷酸和四磷酸的水平。预先用抗霉素 A 处理(一种用于逆转氟化物诱导的高 InsPs 积累的策略),部分减少了氟化物对细胞凋亡以及低 InsPs 水平的影响。总之,我们的研究结果表明,细胞内低磷酸肌醇的水平在细胞凋亡过程中发生了改变。