Dystrophin and muscular dystrophy: Past, present, and future

被引:81
作者
O'Brien, KF
Kunkel, LM
机构
[1] Harvard Univ, Childrens Hosp, Sch Med, Div Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
[3] Harvard Univ, Childrens Hosp, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
Duchenne muscular dystrophy; dystrophin; sarcoglycan; sarcospan; cell transplantation; myoblast therapy;
D O I
10.1006/mgme.2001.3220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Duchenne muscular dystrophy was described in the medical literature in the early 1850s but the molecular basis of the disease was not determined until the late 1980s. The cloning of dystrophin led to the identification of a large complex of proteins that plays an important, although not yet well understood, role in muscle biology. Concomitant with the elucidation of the function of dystrophin and its associated proteins has been the pursuit of therapeutic options for muscular dystrophy. Although there is still no cure for this disorder, great advances are being made in the areas of gene introduction and cell transplant therapy. (C) 2001 Academic Press.
引用
收藏
页码:75 / 88
页数:14
相关论文
共 134 条
[31]  
Cossu G, 1997, HISTOL HISTOPATHOL, V12, P755
[32]   OVEREXPRESSION OF DYSTROPHIN IN TRANSGENIC MDX MICE ELIMINATES DYSTROPHIC SYMPTOMS WITHOUT TOXICITY [J].
COX, GA ;
COLE, NM ;
MATSUMURA, K ;
PHELPS, SF ;
HAUSCHKA, SD ;
CAMPBELL, KP ;
FAULKNER, JA ;
CHAMBERLAIN, JS .
NATURE, 1993, 364 (6439) :725-729
[33]   Molecular and genetic characterization of sarcospan:: insights into sarcoglycan-sarcospan interactions [J].
Crosbie, RH ;
Lim, LE ;
Moore, SA ;
Hirano, M ;
Hays, AP ;
Maybaum, SW ;
Collin, H ;
Dovico, SA ;
Stolle, CA ;
Fardeau, M ;
Tomé, FMS ;
Campbell, KP .
HUMAN MOLECULAR GENETICS, 2000, 9 (13) :2019-2027
[34]   Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex [J].
Crosbie, RH ;
Heighway, J ;
Venzke, DP ;
Lee, JC ;
Campbell, KP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (50) :31221-31224
[35]   ULTRASTRUCTURE OF THE SKELETAL-MUSCLE IN THE X-CHROMOSOME-LINKED DYSTROPHIC (MDX) MOUSE - COMPARISON WITH DUCHENNE MUSCULAR-DYSTROPHY [J].
CULLEN, MJ ;
JAROS, E .
ACTA NEUROPATHOLOGICA, 1988, 77 (01) :69-81
[36]   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
[37]   Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient mice [J].
Deconinck, AE ;
Potter, AC ;
Tinsley, JM ;
Wood, SJ ;
Vater, R ;
Young, C ;
Metzinger, L ;
Vincent, A ;
Slater, CR ;
Davies, KE .
JOURNAL OF CELL BIOLOGY, 1997, 136 (04) :883-894
[38]   A NOVEL DYSTROPHIN ISOFORM IS REQUIRED FOR NORMAL RETINAL ELECTROPHYSIOLOGY [J].
DSOUZA, VN ;
MAN, NT ;
MORRIS, GE ;
KARGES, W ;
PILLERS, DAM ;
RAY, PN .
HUMAN MOLECULAR GENETICS, 1995, 4 (05) :837-842
[39]  
Duchenne G-B, 1861, ELECTRISATION LOCALI
[40]   Progressive muscular dystrophy in α-sarcoglycan-deficient mice [J].
Duclos, F ;
Straub, V ;
Moore, SA ;
Venzke, DP ;
Hrstka, RF ;
Crosbie, RH ;
Durbeej, M ;
Lebakken, CS ;
Ettinger, AJ ;
van der Meulen, J ;
Holt, KH ;
Lim, LE ;
Sanes, JR ;
Davidson, BL ;
Faulkner, JA ;
Williamson, R ;
Campbell, KP .
JOURNAL OF CELL BIOLOGY, 1998, 142 (06) :1461-1471