ABSENCE OF DYSTROPHIN AND SPECTRIN IN REGENERATING MUSCLE-FIBERS FROM BECKER DYSTROPHY PATIENTS

被引:8
作者
FANIN, M [1 ]
PEGORARO, E [1 ]
ANGELINI, C [1 ]
机构
[1] UNIV PADUA, REG NEUROMUSCULAR CTR, DEPT NEUROL, I-35128 PADUA, ITALY
关键词
BECKER MUSCULAR DYSTROPHY; DYSTROPHIN; SPECTRIN; MUSCLE REGENERATION; FETAL MYOSIN; IMMUNOHISTOCHEMISTRY;
D O I
10.1016/0022-510X(94)90208-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We studied muscle biopsies from 36 Becker muscular dystrophy patients, and correlated dystrophin negative fibers with regenerating and degenerating myofibers. Dystrophin immunohistochemistry was used to identify dystrophin-negative and dystrophin-positive fibers. Immunohistochemical staining for fetal myosin and acid ATPase identified regenerating fibers, and calcium glioxalate and beta-spectrin staining identified necrotic fibers. All Becker biopsies contained detectable dystrophin in the majority of muscle fibers. 13 cases (36%) showed no dystrophin negative fibers, 9 cases (25%) showed a generalized, markedly decreased immunostaining pattern, and 14 cases (39%) showed a subset of dystrophin negative fibers (0.3-8% of total). Most dystrophin-negative fibers in Becker muscle were judged to be in the process of regeneration, and not in degeneration. No correlation was observed between the age of the patients and number of dystrophin negative fibers. We conclude that the absence of dystrophin and spectrin labeling in some BMD myofibers is associated with regeneration, probably due to incomplete expression of dystrophin secondary to myofibers immaturity. Our results might be explained by a developmental delayed expression of these two proteins, or by abnormal assembling in membrane's components during regeneration in dystrophy. Furthermore, our results rationalize the recently reported finding of some dystrophin-negative fibers in polymyositis.
引用
收藏
页码:88 / 94
页数:7
相关论文
共 29 条
  • [1] ANGELINI C, 1994, IN PRESS NEUROMUSC D
  • [2] MOSAIC EXPRESSION OF DYSTROPHIN IN SYMPTOMATIC CARRIERS OF DUCHENNES MUSCULAR-DYSTROPHY
    ARAHATA, K
    ISHIHARA, T
    KAMAKURA, K
    TSUKAHARA, T
    ISHIURA, S
    BABA, C
    MATSUMOTO, T
    NONAKA, I
    SUGITA, H
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (03) : 138 - 142
  • [3] IMMUNOCYTOCHEMICAL ANALYSIS OF DYSTROPHIN IN CONGENITAL MUSCULAR-DYSTROPHY
    ARIKAWA, E
    ISHIHARA, T
    NONAKA, I
    SUGITA, H
    ARAHATA, K
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1991, 105 (01) : 79 - 87
  • [4] BEGGS AH, 1991, AM J HUM GENET, V49, P54
  • [5] DYSTROPHIN IS LOCALIZED TO THE PLASMA-MEMBRANE OF HUMAN SKELETAL-MUSCLE FIBERS BY ELECTRON-MICROSCOPIC CYTOCHEMICAL STUDY
    CARPENTER, S
    KARPATI, G
    ZUBRZYCKAGAARN, E
    BULMAN, DE
    RAY, PN
    WORTON, RG
    [J]. MUSCLE & NERVE, 1990, 13 (05) : 376 - 380
  • [6] CHARACTERIZATION OF DYSTROPHIN IN FETUSES AT RISK FOR DUCHENNE MUSCULAR-DYSTROPHY
    CLERK, A
    SEWRY, CA
    DUBOWITZ, V
    STRONG, PN
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1992, 111 (01) : 82 - 91
  • [7] DISTINCT DYSTROPHIN MESSENGER-RNA SPECIES ARE EXPRESSED IN EMBRYONIC AND ADULT-MOUSE SKELETAL-MUSCLE
    DICKSON, G
    PIZZEY, JA
    ELSOM, VE
    LOVE, D
    DAVIES, KE
    WALSH, FS
    [J]. FEBS LETTERS, 1988, 242 (01) : 47 - 52
  • [8] DYSTROPHIN-POSITIVE MYOTUBES IN INNERVATED MUSCLE CULTURES FROM DUCHENNE AND BECKER MUSCULAR-DYSTROPHY PATIENTS
    FANIN, M
    HOFFMAN, EP
    SAAD, FA
    MARTINUZZI, A
    DANIELI, GA
    ANGELINI, C
    [J]. NEUROMUSCULAR DISORDERS, 1993, 3 (02) : 119 - 127
  • [9] EMBRYONIC AND FETAL MYOSINS IN HUMAN SKELETAL-MUSCLE - THE PRESENCE OF FETAL MYOSINS IN DUCHENNE MUSCULAR-DYSTROPHY AND INFANTILE SPINAL MUSCULAR-ATROPHY
    FITZSIMONS, RB
    HOH, JFY
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1981, 52 (2-3) : 367 - 384
  • [10] Geng Y, 1991, Neuromuscul Disord, V1, P125, DOI 10.1016/0960-8966(91)90060-6