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Possible Existence of Lysosome-Like Organella within Mitochondria and Its Role in Mitochondrial Quality Control

机译:线粒体中溶酶样细胞器的可能存在及其在线粒体质量控制中的作用

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摘要

The accumulation of unhealthy mitochondria results in mitochondrial dysfunction, which has been implicated in aging, cancer, and a variety of degenerative diseases. However, the mechanism by which mitochondrial quality is regulated remains unclear. Here, we show that Mieap, a novel p53-inducible protein, induces intramitochondrial lysosome-like organella that plays a critical role in mitochondrial quality control. Mieap expression is directly regulated by p53 and is frequently lost in human cancer as result of DNA methylation. Mieap dramatically induces the accumulation of lysosomal proteins within mitochondria and mitochondrial acidic condition without destroying the mitochondrial structure (designated MALM, for Mieap-induced accumulation of lysosome-like organelles within mitochondria) in response to mitochondrial damage. MALM was not related to canonical autophagy. MALM is involved in the degradation of oxidized mitochondrial proteins, leading to increased ATP synthesis and decreased reactive oxygen species generation. These results suggest that Mieap induces intramitochondrial lysosome-like organella that plays a critical role in mitochondrial quality control by eliminating oxidized mitochondrial proteins. Cancer cells might accumulate unhealthy mitochondria due to p53 mutations and/or Mieap methylation, representing a potential cause of the Warburg effect.
机译:不健康的线粒体的积累会导致线粒体功能障碍,这与衰老,癌症和各种退行性疾病有关。但是,调节线粒体质量的机制尚不清楚。在这里,我们显示Mieap,一种新型的p53诱导蛋白,诱导线粒体内溶酶体样细胞器,在线粒体质量控制中起关键作用。 Mieap表达直接受p53调控,在人类癌症中由于DNA甲基化而经常丢失。 Mieap会在不破坏线粒体结构的情况下(在线粒体中Mieap诱导的溶酶体样细胞器的积累中称为线粒体)破坏线粒体并在酸性条件下诱导线粒体中溶酶体蛋白的积累。 MALM与规范性自噬无关。 MALM参与氧化的线粒体蛋白的降解,导致增加的ATP合成和减少的活性氧生成。这些结果表明,Mieap诱导线粒体内溶酶体样细胞器,通过消除氧化的线粒体蛋白在线粒体质量控制中发挥关键作用。由于p53突变和/或Mieap甲基化,癌细胞可能积聚不健康的线粒体,这代表了Warburg效应的潜在原因。

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