Contribution of the ubiquitin-proteasome pathway to overall muscle proteolysis in hypercatabolic patients

被引:37
作者
Biolo, G
Bosutti, A
Iscra, F
Toigo, G
Gullo, A
Guarnieri, G
机构
[1] Univ Trieste, Ist Clin Med, Trieste, Italy
[2] Univ Trieste, Ist Anestesia Rianimaz & Terapia Antalg, Trieste, Italy
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2000年 / 49卷 / 06期
关键词
D O I
10.1053/meta.2000.6236
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The influence of the gene expression of critical components of the cytoplasmic and lysosomal proteolytic pathways on the rate of protein degradation was evaluated in the leg skeletal muscle of 8 severely traumatized patients. Muscle proteolysis was determined as the intramuscular phenylalanine rate of appearance by L-[ring-H-2(5)]phenylalanine infusion and the leg arteriovenous catheterization technique combined with muscle biopsy. Muscle mRNA levels of UbB polyubiquitin and cathepsin B were determined by reverse transcriptase-competitive polymerase chain reaction and expressed as a percent of the mRNA level of the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase (GAPDH). In the patients, individual values for UbB polyubiquitin mRNA levels directly correlated with the rate of muscle proteolysis (r = .76, P < .05), whereas no correlation (r = .10) was found between cathepsin B mRNA levels and proteolysis. Thus, after trauma, the rate of muscle proteolysis appears to be largely regulated by the ubiquitin-proteasome system at the level of gene transcription. Copyright (C) 2000 by W.B. Saunders Company.
引用
收藏
页码:689 / 691
页数:3
相关论文
共 10 条
  • [1] ANDREU AL, 1995, NUTRITION, V11, P382
  • [2] TRANSMEMBRANE TRANSPORT AND INTRACELLULAR KINETICS OF AMINO-ACIDS IN HUMAN SKELETAL-MUSCLE
    BIOLO, G
    FLEMING, RYD
    MAGGI, SP
    WOLFE, RR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 268 (01): : E75 - E84
  • [3] Molecular regulation of protein catabolism in trauma patients
    Bosutti, A
    Biolo, G
    Toigo, G
    Iscra, F
    Gullo, A
    Giacca, M
    Guarnieri, G
    [J]. CLINICAL NUTRITION, 1999, 18 (02) : 103 - 105
  • [4] Mapping replication origins by quantifying relative abundance of nascent DNA strands using competitive polymerase chain reaction
    Giacca, M
    Pelizon, C
    Falaschi, A
    [J]. METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1997, 13 (03): : 301 - 312
  • [5] Guarnieri G, 1988, Adv Exp Med Biol, V240, P243
  • [6] EVIDENCE THAT LYSOSOMES ARE NOT INVOLVED IN THE DEGRADATION OF MYOFIBRILLAR PROTEINS IN RAT SKELETAL-MUSCLE
    LOWELL, BB
    RUDERMAN, NB
    GOODMAN, MN
    [J]. BIOCHEMICAL JOURNAL, 1986, 234 (01) : 237 - 240
  • [7] Increased mRNA levels for components of the lysosomal, Ca2+-activated, and ATP-ubiquitin-dependent proteolytic pathways in skeletal muscle from head trauma patients
    Mansoor, O
    Beaufrere, B
    Boirie, Y
    Ralliere, C
    Taillandier, D
    Aurousseau, E
    Schoeffler, P
    Arnal, M
    Attaix, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) : 2714 - 2718
  • [8] Mechanisms of disease - Mechanisms of muscle wasting - The role of the ubiquitin-proteasome pathway
    Mitch, WE
    Goldberg, AL
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (25) : 1897 - 1905
  • [9] Muscle wasting in a rat model of long-lasting sepsis results from the activation of lysosomal, Ca2+-activated, and ubiquitin-proteasome proteolytic pathways
    Voisin, L
    Breuille, D
    Combaret, L
    Pouyet, C
    Taillandier, D
    Aurousseau, E
    Obled, C
    Attaix, D
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (07) : 1610 - 1617
  • [10] THE HUMAN UBIQUITIN MULTIGENE FAMILY - SOME GENES CONTAIN MULTIPLE DIRECTLY REPEATED UBIQUITIN CODING SEQUENCES
    WIBORG, O
    PEDERSEN, MS
    WIND, A
    BERGLUND, LE
    MARCKER, KA
    VUUST, J
    [J]. EMBO JOURNAL, 1985, 4 (03) : 755 - 759