Ito S, Inoue K, Yanagisawa N, Kaneko M, Hayashi J
Institute of Biological Sciences, University of Tsukuba, Ibaraki, 305-8572, Japan.
Biochem Biophys Res Commun. 1998 Jun 18;247(2):432-5. doi: 10.1006/bbrc.1998.8800.
Mitochondrial DNA (mtDNA) transfer was carried out from postmortem mouse tissues to mouse mtDNA-less (rho0) cells to determine how long it takes for autolysis of mtDNA after death and whether mtDNA in postmortem tissues can recover its function in rho0 cells. The results showed that mtDNA was stable in postmitotic tissues stored at 4 degreesC. Moreover, mtDNA in postmortem brain tissues stored for up to 1 month still retained functional properties, causing complete recovery of mitochondrial respiratory function, when it was transferred to rho0 cells. These observations suggest that mtDNA in brain tissue can survive for 1 month after death and can start replication and gene expression in rho0 cells without showing any functional defects. This procedure might be applied to human autopsy brain tissues for examination of the influence of accumulated somatic mutations in mtDNA from aged subjects.
将线粒体DNA(mtDNA)从死后的小鼠组织转移到无小鼠mtDNA(rho0)的细胞中,以确定死后mtDNA自溶需要多长时间,以及死后组织中的mtDNA能否在rho0细胞中恢复其功能。结果表明,mtDNA在4℃储存的有丝分裂后组织中是稳定的。此外,储存长达1个月的死后脑组织中的mtDNA在转移到rho0细胞时仍保留功能特性,可使线粒体呼吸功能完全恢复。这些观察结果表明,脑组织中的mtDNA在死后可存活1个月,并能在rho0细胞中开始复制和基因表达,且不显示任何功能缺陷。该程序可能适用于人类尸检脑组织,以检查老年受试者mtDNA中累积的体细胞突变的影响。