Formichi P, Battisti C, Bianchi S, Cardaioli E, Federico A
Department of Neurological and Behavioural Sciences, University of Siena, Italy.
J Submicrosc Cytol Pathol. 2003 Jan;35(1):29-34.
Apoptosis is an evolution-conserved form of cell death essential for development and maintenance of tissue homeostasis. Dysregulation of apoptosis has been implicated in several pathological conditions, including neurodegenerative disorders. The crucial role of mitochondria in regulation of the apoptotic pathway prompted us to investigate the pattern of apoptosis in muscle biopsies from 17 patients with mitochondrial encephaloneuromyopathies caused by mtDNA defects. The results were compared with muscle biopsies from controls and from patients with myopathies without mitochondrial impairment. The terminal deoxynucleotidyl transferase-mediated dUTP nick and labelling (TUNEL) reaction was used as marker of apoptosis. Our findings were very heterogeneous, even between patients with the same mtDNA mutations, suggesting that tissue evaluation of apoptotic process is less useful than in vitro techniques, for investigating the role of apoptosis in mitochondrial pathologies.
细胞凋亡是一种进化保守的细胞死亡形式,对组织稳态的发育和维持至关重要。细胞凋亡失调与多种病理状况有关,包括神经退行性疾病。线粒体在细胞凋亡途径调控中的关键作用促使我们研究17例由线粒体DNA缺陷引起的线粒体脑肌病患者肌肉活检中的细胞凋亡模式。将结果与对照组以及无线粒体损伤的肌病患者的肌肉活检结果进行比较。采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)反应作为细胞凋亡的标志物。我们的研究结果差异很大,即使是具有相同线粒体DNA突变的患者之间也是如此,这表明在研究细胞凋亡在线粒体疾病中的作用时,对凋亡过程进行组织评估不如体外技术有用。