Programming for cytotoxic effector function occurs concomitantly with CD4 extinction during CD8+ T cell differentiation in the thymus

被引:6
作者
Bhandoola, A [1 ]
Kithiganahalli, B [1 ]
Granger, L [1 ]
Singer, A [1 ]
机构
[1] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
关键词
cathepsin C; cathepsin W; cytotoxic lymphocytes; precursor cytotoxic T lymphocyte; thymic selection;
D O I
10.1093/intimm/12.7.1035
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+) T cells are generally specialized to function as helper cells and CD8(+) T cells are generally specialized to function as cytotoxic effector cells. To explain how such concordance is achieved between co-receptor expression and immune function, we considered two possibilities. In one case, immature CD4(+)CD8(+) thymocyte precursors might first down-regulate expression of one co-receptor molecule, with the remaining co-receptor molecule subsequently activating the appropriate helper or cytotoxic functional program. Alternatively, we considered that the same intrathymic signals that selectively extinguished expression of one or the other co-receptor molecule might simultaneously initiate the appropriate helper or cytotoxic functional program. In the present study, we attempted to distinguish between these alternatives by examining thymocyte precursors of CD8(+) T cells for expression of Cathepsin C and Cathepsin W, molecules important for cytotoxic effector function. We report in developing thymocytes that Cathepsin C and Cathepsin W are expressed coordinately with extinction of CD4 co-receptor expression. We conclude that CD4 extinction and initiation of the cytotoxic functional program occurs simultaneously during differentiation of CD8(+) T cells in the thymus.
引用
收藏
页码:1035 / 1040
页数:6
相关论文
共 25 条
[1]   Positive selection as a developmental progression initiated by αβTCR signals that fix TCR specificity prior to lineage commitment [J].
Bhandoola, A ;
Cibotti, R ;
Punt, JA ;
Granger, L ;
Adams, AJ ;
Sharrow, SO ;
Singer, A .
IMMUNITY, 1999, 10 (03) :301-311
[2]  
BROWN GR, 1993, J IMMUNOL, V150, P4733
[3]   FUNCTIONAL COMMITMENT TO HELPER T-CELL LINEAGE PRECEDES POSITIVE SELECTION AND IS INDEPENDENT OF T-CELL RECEPTOR MHC SPECIFICITY [J].
CORBELLA, P ;
MOSKOPHIDIS, D ;
SPANOPOULOU, E ;
MAMALAKI, C ;
TOLAINI, M ;
ITANO, A ;
LANS, D ;
BALTIMORE, D ;
ROBEY, E ;
KIOUSSIS, D .
IMMUNITY, 1994, 1 (04) :269-276
[4]   EVIDENCE FOR A STOCHASTIC MECHANISM IN THE DIFFERENTIATION OF MATURE SUBSETS OF T-LYMPHOCYTES [J].
DAVIS, CB ;
KILLEEN, N ;
CROOKS, MEC ;
RAULET, D ;
LITTMAN, DR .
CELL, 1993, 73 (02) :237-247
[5]   MECHANISM AND BIOLOGICAL SIGNIFICANCE OF CD4-MEDIATED CYTOTOXICITY [J].
HAHN, S ;
GEHRI, R ;
ERB, P .
IMMUNOLOGICAL REVIEWS, 1995, 146 :57-79
[6]   DEVELOPMENT AND SELECTION OF T-CELLS - FACTS AND PUZZLES [J].
KISIELOW, P ;
VONBOEHMER, H .
ADVANCES IN IMMUNOLOGY, VOL 58, 1995, 58 :87-209
[7]  
KOLLER BH, 1990, SCIENCE, V248, P1227, DOI 10.1126/science.2112266
[8]   Human cathepsin W, a putative cysteine protease predominantly expressed in CD8(+) T-lymphocytes [J].
Linnevers, C ;
Smeekens, SP ;
Bromme, D .
FEBS LETTERS, 1997, 405 (03) :253-259
[9]  
Mabee CL, 1998, J IMMUNOL, V160, P5880
[10]   Positive selection of thymocytes bearing alpha beta T cell receptors [J].
Marrack, P ;
Kappler, J .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (02) :250-255