Suicide induced by cytolytic activity controls the differentiation of memory CD8+ T lymphocytes

被引:23
作者
Opferman, JT
Ober, BT
Narayanan, R
Ashton-Rickardt, PG
机构
[1] Gwen Knapp Ctr Lupus & Immunol Res, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[4] Univ Chicago, Ben May Inst Canc Res, Chicago, IL 60637 USA
关键词
apoptosis; cytotoxic T lymphocytes; immunological memory;
D O I
10.1093/intimm/13.4.411
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytotoxic T lymphocytes (CTL) confer protection against intracellular pathogens, yet the mechanism by which some escape activation induced cell death (AICD) and give rise to long-lived memory cells is unclear. We studied the differentiation of transgenic TCR CD8(+) cells into CTL and memory cells using a novel system that allowed us to control cytolytic activity. The perforin/granzyme granules used to lyse targets induced the apoptosis of CTL in a fratricide-independent manner, After adoptive transfer to antigen-free mice, the ability of CTL to give generate memory cells was determined, We found that the extent of cytolysis by a common pool of CTL controlled the differentiation into memory cells, which were only generated under conditions of minimal cytolytic activity, Thus, the differentiation of naive CD8+ cells into memory cells may not depend on the presence on a subset of committed CTL precursors, but rather is controlled by the extent of granule-mediated cytolysis.
引用
收藏
页码:411 / 419
页数:9
相关论文
共 37 条
[1]   Immunological memory and protective immunity: Understanding their relation [J].
Ahmed, R ;
Gray, D .
SCIENCE, 1996, 272 (5258) :54-60
[2]   Selective regulation of apoptosis: the cytotoxic lymphocyte serpin proteinase inhibitor 9 protects against granzyme B-mediated apoptosis without perturbing the Fas cell death pathway [J].
Bird, CH ;
Sutton, VR ;
Sun, JR ;
Hirst, CE ;
Novak, A ;
Kumar, S ;
Trapani, JA ;
Bird, PI .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6387-6398
[3]   ON THE CELLULAR BASIS OF IMMUNOLOGICAL T-CELL MEMORY [J].
BRUNO, L ;
KIRBERG, J ;
VONBOEHMER, H .
IMMUNITY, 1995, 2 (01) :37-43
[4]   CLONAL EXPANSION OF T-CELLS - A CYTOTOXIC T-CELL RESPONSE INVIVO THAT INVOLVES PRECURSOR CELL-PROLIFERATION [J].
DENIZOT, F ;
WILSON, A ;
BATTYE, F ;
BERKE, G ;
SHORTMAN, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :6089-6092
[5]   Inhibition of human caspases by peptide-based and macromolecular inhibitors [J].
Garcia-Calvo, M ;
Peterson, EP ;
Leiting, B ;
Ruel, R ;
Nicholson, DW ;
Thornberry, NA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (49) :32608-32613
[6]  
GREEN LM, 1986, J IMMUNOL, V137, P3488
[7]   Reactive oxygen species regulate activation-induced T cell apoptosis [J].
Hildeman, DA ;
Mitchell, T ;
Teague, TK ;
Henson, P ;
Day, BJ ;
Kappler, J ;
Marrack, PC .
IMMUNITY, 1999, 10 (06) :735-744
[8]   TCR-mediated internalization of peptide-MHC complexes acquired by T cells [J].
Huang, JF ;
Yang, Y ;
Sepulveda, H ;
Shi, WX ;
Hwang, I ;
Peterson, PA ;
Jackson, MR ;
Sprent, J ;
Cai, ZL .
SCIENCE, 1999, 286 (5441) :952-954
[9]   YOPRO-1 PERMITS CYTOFLUOROMETRIC ANALYSIS OF PROGRAMMED CELL-DEATH (APOPTOSIS) WITHOUT INTERFERING WITH CELL VIABILITY [J].
IDZIOREK, T ;
ESTAQUIER, J ;
DEBELS, F ;
AMEISEN, JC .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 185 (02) :249-258
[10]   FAS(CD95) FASL INTERACTIONS REQUIRED FOR PROGRAMMED CELL-DEATH AFTER T-CELL ACTIVATION [J].
JU, ST ;
PANKA, DJ ;
CUI, HL ;
ETTINGER, R ;
ELKHATIB, M ;
SHERR, DH ;
STANGER, BZ ;
MARSHAKROTHSTEIN, A .
NATURE, 1995, 373 (6513) :444-448