Secondary coenzyme Q10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts

被引:120
作者
Cotan, David [1 ,2 ]
Cordero, Mario D. [1 ,2 ]
Garrido-Maraver, Juan [1 ,2 ]
Oropesa-Avila, Manuel [1 ,2 ]
Rodriguez-Hernandez, Angeles [1 ,2 ]
Gomez Izquierdo, Lourdes [3 ]
De la Mata, Mario [1 ,2 ]
De Miguel, Manuel [4 ]
Bautista Lorite, Juan [5 ]
Rivas Infante, Eloy
Jackson, Sandra [6 ]
Navas, Placido [1 ,2 ]
Sanchez-Alcazar, Jose A. [1 ,2 ]
机构
[1] Univ Pablo Olavide, Consejo Super Invest Cient, Ctr Andaluz Biol Desarrollo, Seville 41013, Spain
[2] Univ Pablo Olavide, Consejo Super Invest Cient, Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Raras, Seville 41013, Spain
[3] Hosp Virgen Rocio, Dept Anat Patol, Seville, Spain
[4] Univ Seville, Fac Med, Dept Citol & Histol Normal & Patol, Seville, Spain
[5] Hosp Sagrado Corazon, Seville, Spain
[6] Uniklinikum CG Carus, Dept Neurol, Dresden, Germany
关键词
autophagy; free radicals; mitochondrial diseases; STROKE-LIKE EPISODES; TRANSFER RNALEU(UUR) GENE; PERMEABILITY TRANSITION; LACTIC-ACIDOSIS; PROTEIN-SYNTHESIS; TRANSFER-RNA; CELL-DEATH; AUTOPHAGY; MUTATION; DNA;
D O I
10.1096/fj.10-165340
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a mitochondrial disease most usually caused by point mutations in tRNA genes encoded by mtDNA. Here, we report on how this mutation affects mitochondrial function in primary fibroblast cultures established from 2 patients with MELAS who harbored the A3243G mutation. Both mitochondrial respiratory chain enzyme activities and coenzyme Q(10) (CoQ) levels were significantly decreased in MELAS fibroblasts. A similar decrease in mitochondrial membrane potential was found in intact MELAS fibroblasts. Mitochondrial dysfunction was associated with increased oxidative stress and the activation of mitochondrial permeability transition (MPT), which triggered the degradation of impaired mitochondria. Furthermore, we found defective autophagosome elimination in MELAS fibroblasts. Electron and fluorescence microscopy studies confirmed a massive degradation of mitochondria and accumulation of autophagosomes, suggesting mitophagy activation and deficient autophagic flux. Transmitochondrial cybrids harboring the A3243G mutation also showed CoQ deficiency and increased autophagy activity. All these abnormalities were partially restored by CoQ supplementation. Autophagy in MELAS fibroblasts was also abolished by treatment with antioxidants or cyclosporine, suggesting that both reactive oxygen species and MPT participate in this process. Furthermore, prevention of autophagy in MELAS fibroblasts resulted in apoptotic cell death, suggesting a protective role of autophagy in MELAS fibroblasts.-Cotan, D., Cordero, M. D., Garrido-Maraver, J., Oropesa-Avila, M., Rodriguez-Hernandez, A., Gomez Izquierdo, L., De la Mata, M., De Miguel, M., Bautista Lorite, J., Rivas Infante, E., Jackson, S., Navas, P., Sanchez-Alcazar, J. A. Secondary coenzyme Q10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts. FASEB J. 25, 2669-2687 (2011). www.fasebj.org
引用
收藏
页码:2669 / 2687
页数:19
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