TYPE OF LYMPHOCYTES AFFECTED BY THE ISLET-ACTIVATING PROTEIN (IAP)

被引:1
作者
OHTA, Y
NAKAGAWA, Y
SAIJO, T
机构
[1] Biology Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd., Yodogawa-ku, Osaka, 532, 17-85, Jusohonmachi
来源
IMMUNOPHARMACOLOGY | 1990年 / 19卷 / 03期
关键词
Cytokine; Flow cytometry; IAP; T lymphocyte;
D O I
10.1016/0162-3109(90)90069-Q
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
By flow cytometric analysis, we identified the subclass of lymphocytes that proliferates in response to islet-activating protein (IAP), both in vitro (human peripheral blood mononuclear cells, MNC, cultured with IAP) and in vivo (peripheral blood MNC derived from A/J mice treated with IAP). IAP caused a preferential proliferation of CD8+ T cells. These cells expressed the IL-2 receptors on their surface. CD4+ CD8+ T cells could also be detected in these cultures. IAP caused human MNC to produce IL-1 and to induce expression of HLA-DR antigen. These effects may play an important role in the T-cell proliferation induced by IAP, although IAP by itself suppressed the proliferative action of IL-1 in mouse thymocytes. IAP induced proliferation of the purified CD4+ cells but had a smaller effect on the purified CD8+ cells. This suggests that the proliferation of CD8+ cells in IAP-treated MNC depends on the function of other types of cell, e.g. CD4+ cell and macrophage. © 1990.
引用
收藏
页码:197 / 205
页数:9
相关论文
共 36 条
[21]   GUANINE-NUCLEOTIDE ACTIVATION AND INHIBITION OF ADENYLATE-CYCLASE AS MODIFIED BY ISLET-ACTIVATING PROTEIN, PERTUSSIS TOXIN, IN MOUSE-3T3 FIBROBLASTS [J].
MURAYAMA, T ;
KATADA, T ;
UI, M .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1983, 221 (02) :381-390
[22]  
MURAYAMA T, 1983, J BIOL CHEM, V258, P3319
[23]  
OPPENHEIM JJ, 1982, FED PROC, V41, P257
[24]   INTERLEUKIN-4 MEDIATES CD8 INDUCTION ON HUMAN CD4+ T-CELL CLONES [J].
PALIARD, X ;
MALEFIJT, RD ;
DEVRIES, JE ;
SPITS, H .
NATURE, 1988, 335 (6191) :642-644
[25]   SEPARATION OF FUNCTIONAL SUBSETS OF HUMAN T-CELLS BY A MONOCLONAL ANTIBODY [J].
REINHERZ, EL ;
KUNG, PC ;
GOLDSTEIN, G ;
SCHLOSSMAN, SF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (08) :4061-4065
[26]   ALPHA-BETA T-CELL ANTIGEN RECEPTOR GENE AND PROTEIN EXPRESSION OCCURS AT EARLY STAGES OF THYMOCYTE DIFFERENTIATION [J].
RICHIE, ER ;
MCENTIRE, B ;
CRISPE, N ;
KIMURA, J ;
LANIER, LL ;
ALLISON, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (04) :1174-1178
[27]   THE MAJOR HISTOCOMPATIBILITY COMPLEX-RESTRICTED ANTIGEN RECEPTOR ON T-CELLS .7. DISTRIBUTION ON THYMUS AND PERIPHERAL T-CELLS [J].
ROEHM, N ;
HERRON, L ;
CAMBIER, J ;
DIGUISTO, D ;
HASKINS, K ;
KAPPLER, J ;
MARRACK, P .
CELL, 1984, 38 (02) :577-584
[28]  
ROSOFF PM, 1987, J IMMUNOL, V139, P2419
[29]  
SATO H, 1983, Journal of Microbiological Methods, V1, P99, DOI 10.1016/0167-7012(83)90020-9
[30]   EFFECTS OF BORDETELLA-PERTUSISS COMPONENTS ON IGE AND IGG1 RESPONSES [J].
SEKIYA, K .
MICROBIOLOGY AND IMMUNOLOGY, 1983, 27 (11) :905-915