Berezhnov Alexey V, Soutar Marc P M, Fedotova Evgeniya I, Frolova Maria S, Plun-Favreau Helene, Zinchenko Valery P, Abramov Andrey Y
From the Department of Intracellular Signaling, Institute of Cell Biophysics Russian Academy of Sciences, Pushchino, Moscow Region, 142290 Russian Federation and.
Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, United Kingdom.
J Biol Chem. 2016 Apr 15;291(16):8701-8. doi: 10.1074/jbc.M115.691774. Epub 2016 Feb 18.
The specific autophagic elimination of mitochondria (mitophagy) plays the role of quality control for this organelle. Deregulation of mitophagy leads to an increased number of damaged mitochondria and triggers cell death. The deterioration of mitophagy has been hypothesized to underlie the pathogenesis of several neurodegenerative diseases, most notably Parkinson disease. Although some of the biochemical and molecular mechanisms of mitochondrial quality control are described in detail, physiological or pathological triggers of mitophagy are still not fully characterized. Here we show that the induction of mitophagy by the mitochondrial uncoupler FCCP is independent of the effect of mitochondrial membrane potential but dependent on acidification of the cytosol by FCCP. The ionophore nigericin also reduces cytosolic pH and induces PINK1/PARKIN-dependent and -independent mitophagy. The increase of intracellular pH with monensin suppresses the effects of FCCP and nigericin on mitochondrial degradation. Thus, a change in intracellular pH is a regulator of mitochondrial quality control.
线粒体的特异性自噬清除(线粒体自噬)对该细胞器起到质量控制的作用。线粒体自噬失调会导致受损线粒体数量增加并引发细胞死亡。线粒体自噬功能的恶化被认为是几种神经退行性疾病发病机制的基础,最显著的是帕金森病。尽管线粒体质量控制的一些生化和分子机制已被详细描述,但线粒体自噬的生理或病理触发因素仍未完全明确。在此我们表明,线粒体解偶联剂FCCP诱导的线粒体自噬与线粒体膜电位的影响无关,而是依赖于FCCP引起的胞质酸化。离子载体尼日利亚菌素也会降低胞质pH值并诱导依赖和不依赖PINK1/PARKIN的线粒体自噬。莫能菌素使细胞内pH值升高会抑制FCCP和尼日利亚菌素对线粒体降解的作用。因此,细胞内pH值的变化是线粒体质量控制的一个调节因子。