| Project/Area Number |
07670230
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Experimental pathology
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| Research Institution | Kinki University (1996)
Mie University (1995) |
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Principal Investigator |
MIYAZAWA Masaaki Kinki Univ.School of Med., Dept.of Immunology, Professor, 医学部, 教授 (60167757)
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥2,100,000 (Direct Cost: ¥2,100,000)
Fiscal Year 1996: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1995: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | Autoantibodies / go70 / Tissue injury / Platelets / Endogenous viruses / Monoclonal antibody / Antigenic epitope / 糸球体 |
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| Research Abstract |
1. Mechanisms of the development of glomerular lesions induced by transplantation of anti-gp70 antibody-producing hybridomas : Purified IgG molecules of the nephritogenic anti-gp70 monoclonal antibodies were injected into NZW and C57BL/6 strains of mice. Glomerular lesions were observed only in NZW mice that express a high level of serum gp70. Thus, gp70-anti-gp70 immune complexes seems to be involved in the development of glomerular lesions.
2. Localization of antigenic epitopes recognized by nephritogenic anti-gp70 monoclonal antibodies : By expressing chimeras of xenotropic and polytropic viral env genes, antigenic epitopes recognized by most of the nephritogenic anti-gp70 monoclonal antibodies were mapped to the N-terminal one third of the xenotropic viral gp70.
3. Expression of endogenous retroviral env gene products on platelets : Some of the pathogenic anti-gp70 monoclonal antibodies induce thrombocytopenia associated with systemic hemorrhage when injected into normal mice. Therefore, possible expression of endogenous retroviral gp70 on platelets was tested by FACS analysis. Peripheral blood platelets of normal and MRL strains of mice express several different endogenous retroviral env gene products on their surface. Platelets were aggregated in vivo in small vessels as demonstrated by electron microscopic examination of antibody-injected mice.
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