CHARACTERIZATION OF THE PROLIFERATIVE RESPONSE OF A CD4-8- THYMIC T-LYMPHOMA CELL-LINE TO STIMULATION BY THYMIC CELLULAR-ELEMENTS

被引:0
作者
PINTO, VB
ROCK, KL
机构
[1] HARVARD UNIV,MED CTR,DEPT PATHOL,BOSTON,MA 02215
[2] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DEPT LYMPHOCYTE BIOL,BOSTON,MA 02115
关键词
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
E710.2 is a cloned T cell line that was isolated from an AKR/J thymic tumor. This clone expresses Thy-1, heat-stable Ag, and the CD3/TCR complex but does not express CD4 or CD8. When the E710.2 cell line is injected into syngeneic mice, it grows as a malignant tumor in lymphoid organs and the thymus. In contrast, this cell line does not grow in vitro under standard culture conditions. This latter property allowed us to analyze the in vitro responsiveness of this CD4-CD8- cell line to stimulation by pharmacologic agents and cellular elements from the spleen and thymus. E710.2 cells proliferate when stimulated with phorbol esters or when cocultured with thymocytes or splenocytes. We could not detect soluble stimulatory factors in cultures of E710.2 and/or lymphoid cells, suggesting that cell contact might be required for this response. The stimulatory activity in thymus and spleen appears to be broadly expressed, because all cell subsets that were examined from these tissues stimulate this cell line. The stimulation of E710.2 cells is not MHC-restricted and is not inhibited by anti-MHC mAb. Furthermore, the responsiveness of these cells is not decreased when the TCR/CD3 complex is modulated from the cell surface. Similarly, TCR/ CD3-deficient E710.2 variant clones retain their responsiveness to thymic and splenic cell stimulation. These findings suggest that there is a TCR-independent pathway of activation in E710.2 that is stimulated by a broadly expressed, non-MHC-encoded molecule(s).
引用
收藏
页码:42 / 49
页数:8
相关论文
共 51 条
[1]  
BAMEZAI A, 1988, J IMMUNOL, V141, P1423
[2]  
BATTACHARYA A, 1981, J IMMUNOL, V127, P2488
[3]   CHARACTERIZATION OF MURINE THYMOCYTES WITH CD3-ASSOCIATED T-CELL RECEPTOR STRUCTURES [J].
BLUESTONE, JA ;
PARDOLL, D ;
SHARROW, SO ;
FOWLKES, BJ .
NATURE, 1987, 326 (6108) :82-84
[4]   AN EXTENSION OF 51CR-RELEASE ASSAY FOR ESTIMATION OF MOUSE CYTOTOXINS [J].
BOYLE, W .
TRANSPLANTATION, 1968, 6 (06) :761-&
[5]  
BRUCE J, 1981, J IMMUNOL, V127, P2496
[6]   DEVELOPMENTALLY REGULATED EXPRESSION OF T-CELL RECEPTOR BETA-CHAIN VARIABLE DOMAINS IN IMMATURE THYMOCYTES [J].
BUDD, RC ;
MIESCHER, GC ;
HOWE, RC ;
LEES, RK ;
BRON, C ;
MACDONALD, HR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (02) :577-582
[7]  
CEREDIG R, 1982, J EXP MED, V155, P358, DOI 10.1084/jem.155.2.358
[8]   CHARACTERIZATION OF MONOCLONAL-ANTIBODIES REACTIVE WITH MURINE LEUKEMIA VIRUSES - USE IN ANALYSIS OF STRAINS OF FRIEND MCF AND FRIEND ECOTROPIC MURINE LEUKEMIA-VIRUS [J].
CHESEBRO, B ;
BRITT, W ;
EVANS, L ;
WEHRLY, K ;
NISHIO, J ;
CLOYD, M .
VIROLOGY, 1983, 127 (01) :134-148
[9]   DIFFERENTIATION POTENTIAL OF SUBSETS OF CD4-8- THYMOCYTES [J].
CRISPE, IN ;
MOORE, MW ;
HUSMANN, LA ;
SMITH, L ;
BEVAN, MJ ;
SHIMONKEVITZ, RP .
NATURE, 1987, 329 (6137) :336-339
[10]   LYMPHOCYTE FUNCTION-ASSOCIATED ANTIGEN-1 (LFA-1) - A SURFACE-ANTIGEN DISTINCT FROM LYT-2,3 THAT PARTICIPATES IN LYMPHOCYTE-T-MEDIATED KILLING [J].
DAVIGNON, D ;
MARTZ, E ;
REYNOLDS, T ;
KURZINGER, K ;
SPRINGER, TA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (07) :4535-4539