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线粒体疾病:历史、生物化学及伦敦视角

Mitochondrial disease: a historical, biochemical, and London perspective.

作者信息

Land John M, Morgan-Hughes John A, Hargreaves Iain, Heales Simon J R

机构信息

Neurometabolic Unit, Box 105, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG.

出版信息

Neurochem Res. 2004 Mar;29(3):483-91. doi: 10.1023/b:nere.0000014819.53972.b0.

Abstract

Roland Luft is credited with describing the first truly mitochondrial disorder in the late 1950s and early 1960s. Cases such as his have proven to be exceptionally rare. Some years later, methods of mitochondrial analysis--enzymatic, polarographic, and spectroscopic, which had been developed primarily by groups in Philadelphia--were applied to the study of mitochondria isolated from skeletal muscle biopsies of patients thought to have defects of oxidative phosphorylation. In the vanguard of these investigations were groups in New York and London. John Clark led the latter group. Application of biochemical studies, more recently supplemented by molecular mtDNA and nuclear DNA studies, have revealed that mitochondrial disorders are among the most common of all metabolic disorders.

摘要

罗兰·卢夫因在20世纪50年代末和60年代初描述了首例真正的线粒体疾病而受到赞誉。像他所描述的这种病例已被证明极为罕见。几年后,主要由费城的研究团队开发的线粒体分析方法——酶法、极谱法和光谱法——被应用于对从被认为存在氧化磷酸化缺陷患者的骨骼肌活检样本中分离出的线粒体的研究。纽约和伦敦的研究团队走在了这些研究的前沿。约翰·克拉克带领了伦敦的那个团队。生化研究的应用,最近又得到线粒体DNA和核DNA分子研究的补充,揭示出线粒体疾病是所有代谢性疾病中最常见的疾病之一。

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