Clark K M, Watt D J, Lightowlers R N, Johnson M A, Relvas J B, Taanman J W, Turnbull D M
Department of Neurology, Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4HH, United Kingdom.
J Clin Invest. 1998 Dec 15;102(12):2090-5. doi: 10.1172/JCI944.
Defects of the mitochondrial genome are important causes of disease. Despite major advances in our investigation of patients, there is no effective therapy. Progress in this area is limited by the absence of any animal models in which we can evaluate treatment. To develop such a model we have injected human myoblasts into the tibialis anterior of SCID mice after inducing necrosis. After injection of normal human myoblasts, regenerating fibers expressed human beta-spectrin, confirming they were derived from fusion of human myoblasts. The stability of the muscle fibers was inferred by demonstrating the formation of motor end plates on the regenerating fibers. In addition, we show the presence of human cytochrome c oxidase subunit II, which is encoded by the mitochondrial genome, in the regenerated fibers. After injection of human myoblasts containing either the A8344G or the T8993C heteroplasmic mitochondrial DNA mutations, human beta-spectrin positive fibers were found to contain the mutation at a similar level to the injected myoblasts. These studies highlight the potential value of this model for the study of mitochondrial DNA defects.
线粒体基因组缺陷是疾病的重要病因。尽管我们在对患者的研究方面取得了重大进展,但仍没有有效的治疗方法。该领域的进展受到缺乏可用于评估治疗的动物模型的限制。为了开发这样一种模型,我们在诱导坏死之后将人成肌细胞注射到SCID小鼠的胫前肌中。注射正常人成肌细胞后,再生纤维表达人β-血影蛋白,证实它们源自人成肌细胞的融合。通过证明再生纤维上运动终板的形成来推断肌纤维的稳定性。此外,我们在再生纤维中发现了由线粒体基因组编码的人细胞色素c氧化酶亚基II。在注射含有A8344G或T8993C异质性线粒体DNA突变的人成肌细胞后,发现人β-血影蛋白阳性纤维中的突变水平与注射的成肌细胞相似。这些研究突出了该模型在研究线粒体DNA缺陷方面的潜在价值。