DYSTROPHIN POSITIVE FIBERS IN DUCHENNE DYSTROPHY - ORIGIN AND CORRELATION TO CLINICAL COURSE

被引:48
作者
FANIN, M
DANIELI, GA
CADALDINI, M
MIORIN, M
VITIELLO, L
ANGELINI, C
机构
[1] UNIV PADUA,DEPT NEUROL,I-35128 PADUA,ITALY
[2] UNIV PADUA,DEPT BIOL,PADUA,ITALY
关键词
DUCHENNE MUSCULAR DYSTROPHY; DYSTROPHIN; REVERTED FIBERS; DUPLICATION;
D O I
10.1002/mus.880181007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In 132 DMD muscle biopsies we investigated the presence of dystrophin-positive fibers and the relationship of dystrophin immunohistochemical pattern to the clinical severity of the disease. Reverted fibers were detected in 37% of patients; their prevalence increased significantly in each biopsy with age of patients. We suggest that reversion occurs in satellite cells, when muscle differentiation is completed. The longitudinal extent of dystrophin-positive domain spans a maximum length of 900 mu m. No correlation was found between the presence of reverted fibers and the clinical severity of DMD, whereas a milder form of Duchenne dystrophy was observed in patients showing a faint reaction in all fibers. The occurrence of reverted fibers is independent of the type of gene mutation; however, a higher proportion of cases with reverted fibers was found among patients with gene duplications. (C) 1995 John Wiley & Sons, Inc.
引用
收藏
页码:1115 / 1120
页数:6
相关论文
共 27 条
[1]   CLINICAL-MOLECULAR CORRELATION IN 104 MILD X-LINKED MUSCULAR-DYSTROPHY PATIENTS - CHARACTERIZATION OF SUBCLINICAL PHENOTYPES [J].
ANGELINI, C ;
FANIN, M ;
PEGORARO, E ;
FREDA, MP ;
CADALDINI, M ;
MARTINELLO, F .
NEUROMUSCULAR DISORDERS, 1994, 4 (04) :349-358
[2]  
ARIKAWAHIRASAWA E, 1994, MUSCLE NERVE S, V1, P95
[3]   DYSTROPHIN EXPRESSION AND SOMATIC REVERSION IN PREDNISONE-TREATED AND UNTREATED DUCHENNE DYSTROPHY [J].
BURROW, KL ;
COOVERT, DD ;
KLEIN, CJ ;
BULMAN, DE ;
KISSEL, JT ;
RAMMOHAN, KW ;
BURGHES, AHM ;
MENDELL, JR .
NEUROLOGY, 1991, 41 (05) :661-666
[4]   DIRECT RETROVIRAL-MEDIATED TRANSFER OF A DYSTROPHIN MINIGENE INTO MDX MOUSE MUSCLE INVIVO [J].
DUNCKLEY, MG ;
WELLS, DJ ;
WALSH, FS ;
DICKSON, G .
HUMAN MOLECULAR GENETICS, 1993, 2 (06) :717-723
[5]   MEMBRANE ORGANIZATION OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX [J].
ERVASTI, JM ;
CAMPBELL, KP .
CELL, 1991, 66 (06) :1121-1131
[6]   PREVALENCE OF DYSTROPHIN-POSITIVE FIBERS IN 85 DUCHENNE MUSCULAR-DYSTROPHY PATIENTS [J].
FANIN, M ;
DANIELI, GA ;
VITIELLO, L ;
SENTER, L ;
ANGELINI, C .
NEUROMUSCULAR DISORDERS, 1992, 2 (01) :41-45
[7]   ABSENCE OF DYSTROPHIN AND SPECTRIN IN REGENERATING MUSCLE-FIBERS FROM BECKER DYSTROPHY PATIENTS [J].
FANIN, M ;
PEGORARO, E ;
ANGELINI, C .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1994, 123 (1-2) :88-94
[8]   NORMAL DYSTROPHIN TRANSCRIPTS DETECTED IN DUCHENNE MUSCULAR-DYSTROPHY PATIENTS AFTER MYOBLAST TRANSPLANTATION [J].
GUSSONI, E ;
PAVLATH, GK ;
LANCTOT, AM ;
SHARMA, KR ;
MILLER, RG ;
STEINMAN, L ;
BLAU, HM .
NATURE, 1992, 356 (6368) :435-438
[9]   SOMATIC REVERSION SUPPRESSION OF THE MOUSE MDX PHENOTYPE INVIVO [J].
HOFFMAN, EP ;
MORGAN, JE ;
WATKINS, SC ;
PARTRIDGE, TA .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1990, 99 (01) :9-25
[10]  
Hu Xiuyuan, 1992, Human Mutation, V1, P3, DOI 10.1002/humu.1380010103