The eyes of mito-mouse: Mouse models of mitochondrial disease

被引:7
作者
Biousse, V
Pardue, MT
Wallace, DC
Newman, NJ
机构
[1] Emory Univ, Ctr Eye, Sch Med, Neuroophthalmol Unit,Dept Ophthalmol, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Dept Neurol, Atlanta, GA 30322 USA
[3] Emory Univ, Sch Med, Dept Neurol Surg, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Atlanta VA Med Ctr, Atlanta, GA 30322 USA
[5] Emory Univ, Sch Med, Ctr Mol Med, Atlanta, GA 30322 USA
关键词
D O I
10.1097/00041327-200212000-00005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The recent creation of several mouse models of mitochondrial diseases has provided new insights into the understanding of human mitochondrial disorders. Whether these animals have clinical or histologic ophthalmologic abnormalities is of great interest given the high frequency of such abnormalities in humans with mitochondrial disorders. In this article, we describe the currently available mouse models for mitochondrial diseases with special emphasis on their ocular phenotype. These mouse models demonstrate multiple and varied ophthalmologic manifestations.
引用
收藏
页码:279 / 285
页数:7
相关论文
共 42 条
[1]   The structure of posterior subcapsular cataracts in the Royal College of Surgeons (RCS) rats [J].
Al-Ghoul, KJ ;
Novak, LA ;
Kuszak, JR .
EXPERIMENTAL EYE RESEARCH, 1998, 67 (02) :163-177
[2]   Neuro-ophthalmology of mitochondrial diseases [J].
Biousse, V ;
Newman, NJ .
SEMINARS IN NEUROLOGY, 2001, 21 (03) :275-291
[3]   DIFFERENT NUCLEOTIDE CHANGES IN THE LARGE RIBOSOMAL-RNA GENE OF THE MITOCHONDRIAL-DNA CONFER CHLORAMPHENICOL RESISTANCE ON 2 HUMAN CELL-LINES [J].
BLANC, H ;
ADAMS, CW ;
WALLACE, DC .
NUCLEIC ACIDS RESEARCH, 1981, 9 (21) :5785-5795
[4]  
Carta A, 2000, ARCH OPHTHALMOL-CHIC, V118, P1441
[5]   OCULAR CLINICOPATHOLOGICAL STUDY OF THE MITOCHONDRIAL ENCEPHALOMYOPATHY OVERLAP SYNDROMES [J].
CHANG, TS ;
JOHNS, DR ;
WALKER, D ;
DELACRUZ, Z ;
MAUMENEE, IH ;
GREEN, R .
ARCHIVES OF OPHTHALMOLOGY, 1993, 111 (09) :1254-1262
[6]  
CHINNERY PF, 1999, LANCET S1, V354, P17
[7]   Diseases of oxidative phosphorylation due to mtDNA mutations [J].
DiMauro, S ;
Andreu, AL ;
Musumeci, O ;
Bonilla, E .
SEMINARS IN NEUROLOGY, 2001, 21 (03) :251-260
[8]  
EAGLE RC, 1982, OPHTHALMOLOGY, V89, P1433
[9]   Mitochondrial disease in mouse results in increased oxidative stress [J].
Esposito, LA ;
Melov, S ;
Panov, A ;
Cottrell, BA ;
Wallace, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :4820-4825
[10]   A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator [J].
Graham, BH ;
Waymire, KG ;
Cottrell, B ;
Trounce, IA ;
MacGregor, GR ;
Wallace, DC .
NATURE GENETICS, 1997, 16 (03) :226-234