Commentary: extraocular muscle sparing in muscular dystrophy: a critical evaluation of potential protective mechanisms

被引:28
作者
Porter, JD
机构
[1] Univ Kentucky, Med Ctr, Dept Neurobiol & Anat, Lexington, KY 40536 USA
[2] Univ Kentucky, Dept Ophthalmol, Lexington, KY 40536 USA
关键词
Duchenne muscular dystrophy; congenital muscular dystrophy; dystrophin; merosin; extraocular muscle;
D O I
10.1016/S0960-8966(98)00015-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Muscles or muscle groups exhibiting responses to neuromuscular disease that are unlike those of other skeletal muscles may provide novel information about pathogenesis leading to improved treatment strategies. The author's laboratory studies the relationship between the unique phenotype of the extraocular muscles and their selective sparing or targeting in neuromuscular disease. This commentary evaluates the evidence for and against four hypotheses for the selective protection of extraocular muscle in Duchenne muscular dystrophy (DMD) and merosin-deficient congenital muscular dystrophy(CMD). (C) 1998 Elsevier Science B.V.
引用
收藏
页码:198 / 203
页数:6
相关论文
共 39 条
[1]  
Banker BQ, 1994, MYOLOGY, V2
[2]   NITRIC-OXIDE SYNTHASE COMPLEXED WITH DYSTROPHIN AND ABSENT FROM SKELETAL-MUSCLE SARCOLEMMA IN DUCHENNE MUSCULAR-DYSTROPHY [J].
BRENMAN, JE ;
CHAO, DS ;
XIA, HH ;
ALDAPE, K ;
BREDT, DS .
CELL, 1995, 82 (05) :743-752
[3]  
Brueckner JK, 1996, J MUSCLE RES CELL M, V17, P297
[4]  
BRUECKNER JK, 1997, J MUSCLE RES CELL M, V18, P203
[5]   3 MUSCULAR-DYSTROPHIES - LOSS OF CYTOSKELETON EXTRACELLULAR-MATRIX LINKAGE [J].
CAMPBELL, KP .
CELL, 1995, 80 (05) :675-679
[6]   Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy [J].
Deconinck, AE ;
Rafael, JA ;
Skinner, JA ;
Brown, SC ;
Potter, AC ;
Metzinger, L ;
Watt, DJ ;
Dickson, JG ;
Tinsley, JM ;
Davies, KE .
CELL, 1997, 90 (04) :717-727
[7]   Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice [J].
Deconinck, N ;
Tinsley, J ;
DeBacker, F ;
Fisher, R ;
Kahn, D ;
Phelps, S ;
Davies, K ;
Gillis, JM .
NATURE MEDICINE, 1997, 3 (11) :1216-1221
[8]   Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: A model for Duchenne muscular dystrophy [J].
Grady, RM ;
Teng, HB ;
Nichol, MC ;
Cunningham, JC ;
Wilkinson, RS ;
Sanes, JR .
CELL, 1997, 90 (04) :729-738
[9]   OXYRADICAL DAMAGE AND MITOCHONDRIAL ENZYME-ACTIVITIES IN THE MDX MOUSE [J].
HAUSER, E ;
HOGER, H ;
BITTNER, R ;
WIDHALM, K ;
HERKNER, K ;
LUBEC, G .
NEUROPEDIATRICS, 1995, 26 (05) :260-262
[10]   THE DYSTROPHIN-RELATED PROTEIN, UTROPHIN, IS EXPRESSED ON THE SARCOLEMMA OF REGENERATING HUMAN SKELETAL-MUSCLE FIBERS IN DYSTROPHIES AND INFLAMMATORY MYOPATHIES [J].
HELLIWELL, TR ;
MAN, NT ;
MORRIS, GE ;
DAVIES, KE .
NEUROMUSCULAR DISORDERS, 1992, 2 (03) :177-184