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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Mitochondrial DNA deletion mutations in adult mouse cardiac side population cells
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Mitochondrial DNA deletion mutations in adult mouse cardiac side population cells

机译:成年小鼠心脏侧细胞中线粒体DNA缺失突变

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摘要

We investigated the presence and potential role of mitochondrial DNA (mtDNA) deletion mutations in adult cardiac stem cells. Cardiac side population (SP) cells were isolated from 12-week-old mice. Standard polymerase chain reaction (PCR) was used to screen for the presence of mtDNA deletion mutations in (a) freshly isolated SP cells and (b) SP cells cultured to passage 10. When present, the abundance of mtDNA deletion mutation was analyzed in single cell colonies. The effect of different levels of deletion mutations on SP cell growth and differentiation was determined. MtDNA deletion mutations were found in both freshly isolated and cultured cells from 12-week-old mice. While there was no significant difference in the number of single cell colonies with mtDNA deletion mutations from any of the groups mentioned above, the abundance of mtDNA deletion mutations was significantly higher in the cultured cells, as determined by quantitative PCR. Within a single clonal cell population, the detectable mtDNA deletion mutations were the same in all cells and unique when compared to deletions of other colonies. We also found that cells harboring high levels of mtDNA deletion mutations (i.e. where deleted mtDNA comprised more than 60% of total mtDNA) had slower proliferation rates and decreased differentiation capacities. Screening cultured adult stem cells for mtDNA deletion mutations as a routine assessment will benefit the biomedical application of adult stem cells.
机译:我们调查了成人心脏干细胞中线粒体DNA(mtDNA)缺失突变的存在和潜在作用。从12周龄的小鼠中分离出心脏侧群体(SP)细胞。使用标准聚合酶链反应(PCR)筛选(a)新鲜分离的SP细胞和(b)培养至第10代的SP细胞中mtDNA缺失突变的存在。当存在时,单次分析mtDNA缺失突变的丰度细胞集落。确定了不同水平的缺失突变对SP细胞生长和分化的影响。在来自12周龄小鼠的新鲜分离和培养的细胞中均发现了MtDNA缺失突变。尽管来自上述任何组的具有mtDNA缺失突变的单细胞集落的数量没有显着差异,但通过定量PCR确定,培养细胞中mtDNA缺失突变的丰度明显更高。在单个克隆细胞群中,与其他菌落的缺失相比,可检测到的mtDNA缺失突变在所有细胞中都是相同的,并且是唯一的。我们还发现具有高水平mtDNA缺失突变的细胞(即缺失的mtDNA占总mtDNA的60%以上)具有较慢的增殖速率和降低的分化能力。作为常规评估,筛选培养的成人干细胞是否存在mtDNA缺失突变,这将有益于成人干细胞的生物医学应用。

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