Contraction-induced injury to single permeabilized muscle fibers from mdx, transgenic mdx, and control mice

被引:105
作者
Lynch, GS
Rafael, JA
Chamberlain, JS
Faulkner, JA
机构
[1] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Physiol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2000年 / 279卷 / 04期
关键词
dystrophin; force deficit; sarcolemma; myofibrils; strain;
D O I
10.1152/ajpcell.2000.279.4.C1290
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Muscle fibers of mdx mice that lack dystrophin are more susceptible to contraction-induced injury, particularly when stretched. In contrast, transgenic mdx (tg-mdx) mice, which overexpress dystrophin, show no morphological or functional signs of dystrophy. Permeabilization disrupts the sarcolemma of fibers from muscles of mdx, tg-mdx, and control mice. We tested the null hypothesis stating that, after single stretches of maximally activated single permeabilized fibers, force deficits do not differ among fibers from extensor digitorum longus muscles of mdx, tg-mdx, or control mice. Fibers were maximally activated by Ca2+ (pCa 4.5) and then stretched through strains of 10%, 20%, or 30% of fiber length (L-f) at a velocity of 0.5 L-f/s. Immediately after each strain, the force deficits were not different for fibers from each of the three groups of mice. When collated with studies of membrane-intact fibers in whole muscles of mdx, tg-mdx, and control mice, these results indicate that dystrophic symptoms do not arise from factors within myofibrils but, rather, from disruption of the sarcolemmal integrity that normally provides protection from contraction-induced injury.
引用
收藏
页码:C1290 / C1294
页数:5
相关论文
共 29 条
  • [1] Rapid recovery following contraction-induced injury to in situ skeletal muscles in mdx mice
    Brooks, SV
    [J]. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1998, 19 (02) : 179 - 187
  • [2] The magnitude of the initial injury induced by stretches of maximally activated muscle fibres of mice and rats increases in old age
    Brooks, SV
    Faulkner, JA
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1996, 497 (02): : 573 - 580
  • [3] CLARKE MSF, 1993, J CELL SCI, V106, P121
  • [4] Transgenic mdx mice expressing dystrophin with a deletion in the actin-binding domain display a ''mild becker'' phenotype
    Corrado, K
    Rafael, JA
    Mills, PL
    Cole, NM
    Faulkner, JA
    Wang, K
    Chamberlain, JS
    [J]. JOURNAL OF CELL BIOLOGY, 1996, 134 (04) : 873 - 884
  • [5] Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene
    Deconinck, N
    Ragot, T
    Marechal, G
    Perricaudet, M
    Gillis, JM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) : 3570 - 3574
  • [6] DIFFERENTIAL EXPRESSION OF MUSCULAR-DYSTROPHY IN DIAPHRAGM VERSUS HINDLIMB MUSCLES OF MDX MICE
    DUPONTVERSTEEGDEN, EE
    MCCARTER, RJ
    [J]. MUSCLE & NERVE, 1992, 15 (10) : 1105 - 1110
  • [7] CHEMICALLY SKINNED MAMMALIAN SKELETAL-MUSCLE .1. STRUCTURE OF SKINNED RABBIT PSOAS
    EASTWOOD, AB
    WOOD, DS
    BOCK, KL
    SORENSON, MM
    [J]. TISSUE & CELL, 1979, 11 (03) : 553 - 566
  • [8] Faulkner JA, 1997, BASIC APPL MYOL, V7, P257
  • [9] Understanding dystrophinopathies:: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse
    Gillis, JM
    [J]. JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1999, 20 (07) : 605 - 625
  • [10] Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vector
    Greelish, JP
    Su, LT
    Lankford, EB
    Burkman, JM
    Chen, HY
    Konig, SK
    Mercier, IM
    Desjardins, PR
    Mitchell, MA
    Zheng, XG
    Leferovich, J
    Gao, GP
    Balice-Gordon, RJ
    Wilson, JM
    Stedman, HH
    [J]. NATURE MEDICINE, 1999, 5 (04) : 439 - 443