| Project/Area Number |
60480179
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| Research Category |
Grant-in-Aid for General Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Immunology
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| Research Institution | Keio University |
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Principal Investigator |
SAITO Kazuhisa Keio University School of Medicine, Professor, 医学部, 教授 (80050946)
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| Co-Investigator(Kenkyū-buntansha) |
TADAKUMA Takushi Keio University School of Medicine, Associate Professor, 医学部, 助教授 (30051626)
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| Project Period (FY) |
1985 – 1987
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| Project Status |
Completed (Fiscal Year 1987)
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| Budget Amount *help |
¥4,400,000 (Direct Cost: ¥4,400,000)
Fiscal Year 1987: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1986: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1985: ¥2,300,000 (Direct Cost: ¥2,300,000)
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| Keywords | ABA-tyrosine / Antigen presentation / Antigen recognition by T cell / Auto-A-reactive T cell / Autoimmune disease / Ia-conjugated liposome / Sopped flow method / T細胞の抗原認識 / Ia抗原 / ABA-tyrosine / propyl-glycine / 自己反応性T細胞クローン / 抗核抗体 |
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| Research Abstract |
1. Even by use of I-A^KK gene-transfected L cells as antigen presenting cells (APC), azobenzenearso- nate-tyrosine (ABA-tyr) specific T cell clones or T hybridomas (I-A^kk restricted) showed increase in DNA synthesis or IL 2 production in respones to ABA-tyr, and these responses were blocked by anti-I-A^KK antibody. 2. To study directly antigen recognition of T cells, we examined changes in Ca^<2+>2 influx and membrane fluidity of T cells after antigen recognition by stopped flow method using fluorescent probes. In the presence of I-A^KK gene-transfected L cells or liposomes conjugated with Ia^KK molecules, ABA-tyr specific T cells showed marked increase in Ca^<2+>2 influx and membrane fluidity within 2 seconds after stimulation with ABA-tyr, and these responses were blocked by anti-I-A^KK antibody. 3. To clarify whether ABA-tyr should bind to Ia molecules before being recognized by T cells, we compared the rate constants of Ca^<2+>2 influx when the order of mixing of T cells, ABA-tyr and APC was changed. The rate constant was almost the same even by change in the order of mixing. These results support the trimolecular complex model of antigen recognition by T cells. 4. Among auto-Ia-reactive T cell clones, noe clone elicited lichen planus-like lesion in the skin of syngeneic mice. Another clone injected i.v. into syngeneic mice caused production of anti-DNA antibody and auto-antibody to erythrocytes. We ate exploring the causes of autoimmune diseases by use of these auto-Ia-reactive T cell clones.
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