Protein degradation and apoptotic death in lymphocytes during Fiv infection: Activation of the ubiquitin-proteasome proteolytic system

被引:15
作者
Piedimonte, G
Crinelli, R
Della Salda, L
Corsi, D
Pennisi, MG
Kramer, L
Casabianca, A
Sarli, G
Bendinelli, M
Marcato, PS
Magnani, M
机构
[1] Univ Messina, Fac Med Vet, Ist Patol Gen & Anat Patol Vet, I-98123 Messina, Italy
[2] Univ Urbino, Ist Chim Biol Giorgio Fornaini, I-61029 Urbino, Italy
[3] Univ Bologna, Fac Med Vet, Bologna, Italy
[4] Univ Parma, Fac Med, I-43100 Parma, Italy
[5] Univ Pisa, Dipartimento Biomed, Pisa, Italy
关键词
apoptotic death; Fiv; lymphocytes; protein degradation; proteasome; ubiquitin;
D O I
10.1006/excr.1999.4410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The movement of a cell through the sequential phases of apoptosis is accompanied by a progressive decrease in cell size with loss in protein mass. In lymphocytes from Hiv-infected persons, protein loss during apoptosis is due to increased protein degradation rather than decreased synthesis. To identify and characterize the proteolytic enzymes or enzyme systems involved in this process, we studied several features of protein turnover in lymphocytes from peripheral blood and lymph nodes during the natural and experimental infection by feline immunodeficiency virus (Fiv), This animal model allowed us to integrate in vivo results with in vitro observations of protein damage. Here we report that protein breakdown in apoptotic cells is concomitant with the activation of the ATP and ubiquitin-dependent multicatalytic system (proteasome). We suggest that proteasome activation is part of the proteolytic cascade in the execution phases of apoptosis in AIDS. (C) 1999 Academic Press.
引用
收藏
页码:381 / 390
页数:10
相关论文
共 48 条
[1]   The acidosis of chronic renal failure activates muscle proteolysis in rats by augmenting transcription of genes encoding proteins of the ATP-dependent ubiquitin-proteasome pathway [J].
Bailey, JL ;
Wang, XN ;
England, BK ;
Price, SR ;
Ding, XY ;
Mitch, WE .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (06) :1447-1453
[2]   ACTIVATION OF THE ATP-UBIQUITIN-PROTEASOME PATHWAY IN SKELETAL-MUSCLE OF CACHECTIC RATS BEARING A HEPATOMA [J].
BARACOS, VE ;
DEVIVO, C ;
HOYLE, DHR ;
GOLDBERG, AL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 268 (05) :E996-E1006
[3]   FELINE IMMUNODEFICIENCY VIRUS - AN INTERESTING MODEL FOR AIDS STUDIES AND AN IMPORTANT CAT PATHOGEN [J].
BENDINELLI, M ;
PISTELLO, M ;
LOMBARDI, S ;
POLI, A ;
GARZELLI, C ;
MATTEUCCI, D ;
CECCHERININELLI, L ;
MALVALDI, G ;
TOZZINI, F .
CLINICAL MICROBIOLOGY REVIEWS, 1995, 8 (01) :87-112
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   Dismantling cell-cell contacts during apoptosis is coupled to a caspase-dependent proteolytic cleavage of beta-catenin [J].
Brancolini, C ;
Lazarevic, D ;
Rodriguez, J ;
Schneider, C .
JOURNAL OF CELL BIOLOGY, 1997, 139 (03) :759-771
[6]   THE UBIQUITIN-PROTEASOME PROTEOLYTIC PATHWAY [J].
CIECHANOVER, A .
CELL, 1994, 79 (01) :13-21
[7]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[8]  
COSTELLI P, 1995, J CLIN INVEST, V95, P2867
[9]  
DAVIES KJA, 1987, J BIOL CHEM, V262, P9895
[10]   TAT PROTEIN OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPRESSES EXPRESSION OF MANGANESE SUPEROXIDE-DISMUTASE IN HELA-CELLS [J].
FLORES, SC ;
MARECKI, JC ;
HARPER, KP ;
BOSE, SK ;
NELSON, SK ;
MCCORD, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7632-7636