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线粒体 DNA 突变会损害红细胞成熟过程中线粒体的清除,导致红细胞破坏增加。

MtDNA mutagenesis impairs elimination of mitochondria during erythroid maturation leading to enhanced erythrocyte destruction.

机构信息

Research Programs Unit, Molecular Neurology, University of Helsinki, Biomedicum-Helsinki, Haartmaninkatu 8, FI-00290 Helsinki, Finland.

1] Department of Molecular and Developmental Medicine, University of Siena, I-53100 Siena, Italy [2] Child Neuropsychiatry Unit, University Hospital Azienda Ospedaliera Universitaria Senese, I-53100 Siena, Italy.

出版信息

Nat Commun. 2015 Mar 9;6:6494. doi: 10.1038/ncomms7494.

Abstract

Haematopoietic progenitor cells show special sensitivity to mitochondrial DNA (mtDNA) mutagenesis, which suggests that increased mtDNA mutagenesis could underlie anemias. Here we show that elevated mtDNA mutagenesis in mice with a proof-reading deficient mtDNA polymerase (PolG) leads to incomplete mitochondrial clearance, with asynchronized iron loading in erythroid precursors, and increased total and free cellular iron content. The resulting Fenton chemistry leads to oxidative damage and premature destruction of erythrocytes by splenic macrophages. Our data indicate that mitochondria actively contribute to their own elimination in reticulocytes and modulate iron loading. Asynchrony of this sequence of events causes severe mitochondrial anaemia by depleting the organism of red blood cells and the bone marrow of iron. Our findings account for the anaemia development in a progeroid mouse model and may have direct relevance to the anemias associated with human mitochondrial disease and ageing.

摘要

造血祖细胞对线粒体 DNA(mtDNA)突变特别敏感,这表明增加的 mtDNA 突变可能是贫血的基础。在这里,我们表明,具有校对缺陷的 mtDNA 聚合酶(PolG)的小鼠中 mtDNA 突变的增加导致不完全的线粒体清除,红系前体细胞中铁的加载不同步,总细胞和游离细胞铁含量增加。由此产生的芬顿化学导致氧化损伤和脾巨噬细胞对红细胞的过早破坏。我们的数据表明,线粒体在网织红细胞中积极促进自身清除,并调节铁的加载。由于该事件序列的不同步,通过耗尽红细胞和骨髓中的铁,导致严重的线粒体贫血。我们的发现解释了进行性老化样小鼠模型中贫血的发展,并且可能与人类线粒体疾病和衰老相关的贫血直接相关。

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