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SCID mice containing muscle with human mitochondrial DNA mutations. An animal model for mitochondrial DNA defects.携带有人线粒体DNA突变肌肉的重症联合免疫缺陷小鼠。线粒体DNA缺陷的动物模型。
J Clin Invest. 1998 Dec 15;102(12):2090-5. doi: 10.1172/JCI944.
2
Identification of the RAG-1 as a suitable mouse model for mitochondrial DNA disease.鉴定RAG-1作为线粒体DNA疾病的合适小鼠模型。
Neuromuscul Disord. 2004 May;14(5):329-36. doi: 10.1016/j.nmd.2004.02.010.
3
Reversal of a mitochondrial DNA defect in human skeletal muscle.
Nat Genet. 1997 Jul;16(3):222-4. doi: 10.1038/ng0797-222.
4
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.线粒体肌病中的细胞凋亡与线粒体增殖有关。
Brain. 2006 May;129(Pt 5):1249-59. doi: 10.1093/brain/awl061. Epub 2006 Mar 14.
5
Mitochondrial Genetics. A clever way to model defects...线粒体遗传学。一种模拟缺陷的巧妙方法……
Nat Rev Genet. 2000 Nov;1(2):84-5. doi: 10.1038/35038505.
6
High efficiency of muscle regeneration after human myoblast clone transplantation in SCID mice.人成肌细胞克隆移植到SCID小鼠后肌肉再生效率高。
J Clin Invest. 1994 Feb;93(2):586-99. doi: 10.1172/JCI117011.
7
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.与线粒体DNA耗竭及胸苷激酶2(TK2)基因纯合突变(T77M)相关的儿童线粒体肌病。
Arch Neurol. 2003 Jul;60(7):1007-9. doi: 10.1001/archneur.60.7.1007.
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Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.一名肢带型肌营养不良症患者肌肉组织中的两种新型线粒体DNA突变。
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[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA].1例线粒体DNA第8993位核苷酸发生T到C点突变的神经源性肌无力、共济失调和色素性视网膜炎(NARP)病例
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本文引用的文献

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A "DIRECT-COLORING" THIOCHOLINE METHOD FOR CHOLINESTERASES.一种用于胆碱酯酶的“直接显色”硫代胆碱法。
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2
Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice.线粒体转录因子A对小鼠的线粒体DNA维持和胚胎发育至关重要。
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Mitochondrial susceptibility to oxidative stress exacerbates cerebral infarction that follows permanent focal cerebral ischemia in mutant mice with manganese superoxide dismutase deficiency.线粒体对氧化应激的易感性会加剧锰超氧化物歧化酶缺乏的突变小鼠永久性局灶性脑缺血后的脑梗死。
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Treatment of mitochondrial disease.线粒体疾病的治疗
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5
A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.一种因腺嘌呤核苷酸转位酶心脏/肌肉同工型缺乏导致的线粒体肌病和心肌病小鼠模型。
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Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids.肽核酸在体外对突变型人类线粒体DNA复制的选择性抑制作用
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Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.雌性生殖系中的随机遗传漂变解释了哺乳动物线粒体DNA的快速分离。
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8
Subunit specific monoclonal antibodies show different steady-state levels of various cytochrome-c oxidase subunits in chronic progressive external ophthalmoplegia.亚基特异性单克隆抗体显示慢性进行性外眼肌麻痹中各种细胞色素c氧化酶亚基的不同稳态水平。
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A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.利氏综合征中线粒体ATP酶6基因的第二个错义突变。
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Mitochondrial encephalomyopathies.线粒体脑肌病
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携带有人线粒体DNA突变肌肉的重症联合免疫缺陷小鼠。线粒体DNA缺陷的动物模型。

SCID mice containing muscle with human mitochondrial DNA mutations. An animal model for mitochondrial DNA defects.

作者信息

Clark K M, Watt D J, Lightowlers R N, Johnson M A, Relvas J B, Taanman J W, Turnbull D M

机构信息

Department of Neurology, Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4HH, United Kingdom.

出版信息

J Clin Invest. 1998 Dec 15;102(12):2090-5. doi: 10.1172/JCI944.

DOI:10.1172/JCI944
PMID:9854044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC509163/
Abstract

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.

摘要

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。