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1 , 2 Among the specific molecules involved in this fine‐tuning, the recent data highlight the peroxisome proliferator‐activated receptor‐γ coactivator (PGC)‐1α, the main regulator of mitochondrial biogenesis, 3 , 4 , 5 the PTEN‐induced putative kinase 1 (PINK1)‐Pakin, 6 that activates protein synthesis in damaged mitochondria, and the ligand‐activated transcription factor aryl hydrocarbon receptor, that functions also as protector from oxidative stress

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