Time-dependent changes in myosin heavy chain mRNA and protein isoforms in unloaded soleus muscle of rat

被引:94
作者
Stevens, L
Sultan, KR
Peuker, H
Gohlsch, B
Mounier, Y
Pette, D [1 ]
机构
[1] Univ Konstanz, Fac Biol, D-78457 Constance, Germany
[2] Univ Sci & Tech Lille Flandres Artois, Lab Plasticite Neuromusculaire, F-59655 Villeneuve Dascq, France
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 277卷 / 06期
关键词
hindlimb suspension; messenger ribonucleic acid; myosin heavy chain isoforms; reverse transcriptase-polymerase chain reaction slow-to-fast transition;
D O I
10.1152/ajpcell.1999.277.6.C1044
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Time-dependent changes in myosin heavy chain (MHC) isoform expression were investigated in rat soleus muscle unloaded by hindlimb suspension. Changes at the mRNA level were measured by RT-PCR and correlated with changes in the pattern of MHC protein isoforms. Protein analyses of whole muscle revealed that MHCI decreased after 7 days, when MHCIIa had increased, reaching a transient maximum by 15 days. Longer periods led to inductions and progressive increases of MHCIId(x) and MHCIIb. mRNA analyses of whole muscle showed that MHCIId(x) displayed the steepest increase after 4 days and continued to rise until 28 days, the longest time period investigated. MHCIIb mRNA followed a similar time course, although at lower levels. MHCI alpha mRNA, present at extremely low levels in control soleus, peaked after 4 days, stayed elevated until 15 days, and then decayed. Immunohistochemistry of 15-day unloaded muscles revealed that MHCI alpha was present in muscle spindles but at low amounts also in extrafusal fibers. The slow-to-fast transitions thus seem to proceed in the order MHCI beta --> MHCIIa --> MHCIId(x) --> MHCIIb. Our findings indicate that MHCI alpha is transiently upregulated in some fibers as an intermediate step during the transition from MHCI beta to MHCIIa.
引用
收藏
页码:C1044 / C1049
页数:6
相关论文
共 36 条
  • [2] Microgravity-induced transformations of myosin isoforms and contractile properties of skeletal muscle
    Caiozzo, VJ
    Haddad, F
    Baker, MJ
    Herrick, RE
    Prietto, N
    Baldwin, KM
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1996, 81 (01) : 123 - 132
  • [3] Novel transitions in MHC isoforms: separate and combined effects of thyroid hormone and mechanical unloading
    Caiozzo, VJ
    Baker, MJ
    Baldwin, KM
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1998, 85 (06) : 2237 - 2248
  • [4] MYOSIN AND TROPONIN CHANGES IN RAT SOLEUS MUSCLE AFTER HINDLIMB SUSPENSION
    CAMPIONE, M
    AUSONI, S
    GUEZENNEC, CY
    SCHIAFFINO, S
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 1993, 74 (03) : 1156 - 1160
  • [5] Upregulation of M-creatine kinase and glyceraldehyde-3-phosphate dehydrogenase:: two markers of muscle disuse
    Cros, N
    Muller, J
    Bouju, S
    Piétu, G
    Jacquet, C
    Dechesne, CA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 276 (02) : R308 - R316
  • [6] CONTROL OF MYOSIN HEAVY-CHAIN EXPRESSION - INTERACTION OF HYPOTHYROIDISM AND HINDLIMB SUSPENSION
    DIFFEE, GM
    HADDAD, F
    HERRICK, RE
    BALDWIN, KM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (06): : C1099 - C1106
  • [7] DIFFEE GM, 1991, AM J PHYSIOL, V260, P528
  • [8] SENSITIVE DETECTION OF MYOSIN HEAVY-CHAIN COMPOSITION IN SKELETAL-MUSCLE UNDER DIFFERENT LOADING CONDITIONS
    FAUTECK, SP
    KANDARIAN, SC
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 268 (02): : C419 - C424
  • [9] Two functionally distinct myosin heavy chain isoforms in slow skeletal muscle fibres
    Galler, S
    Hilber, K
    Gohlsch, B
    Pette, D
    [J]. FEBS LETTERS, 1997, 410 (2-3): : 150 - 152
  • [10] SLOW-TO-FAST TRANSFORMATION OF DENERVATED SOLEUS MUSCLES BY CHRONIC HIGH-FREQUENCY STIMULATION IN THE RAT
    GORZA, L
    GUNDERSEN, K
    LOMO, T
    SCHIAFFINO, S
    WESTGAARD, RH
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1988, 402 : 627 - 649