1996 Fiscal Year Final Research Report Summary
Immunological Function of HLA-G Exepressed on trophoblasts.
Project/Area Number |
07671815
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Obstetrics and gynecology
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Research Institution | Nara Medical University |
Principal Investigator |
ISHITANI Akiko Nara Medical University, Departement of Medicine, Assistant Research er, 医学部, 助手 (40112544)
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Project Period (FY) |
1995 – 1996
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Keywords | HLA-G / placenta / trophoblast / monoclonal antibody / immunohistochemistry / immunosupressor / reproductive immunology |
Research Abstract |
To understand the basic relationship of HLA class I to maternal-placental immune tolerance, we have attempted to dissect the expression of soluble (S) HLA-G from menbrance bound (M) HLA-G and to investigate the expression of other nonclassical class I,specifically HLA-E.Towards this goal, we have developed a set of HLA-G specific monoclonal antibodies which allow the distinction of the soluble and membrane G1 proteins, and have used these and specific anti-HLA-E reagents in immunohisto-chemical staining to localize these three proteins in placental tissue. Further, we used HLA-G specific antibodies to isolate S・HLA-G and M・HLA-G directly from placental tissue in order to examine bound peptides. 1. Expression of HLA-G and HLA-E Immunohistochemical staining of placenta demonstrated that S・HLA-G was found expressed in syncyciotrophoblasts, cytotrophoblasts, and extravillous cytotrophoblasts and was also apparent in maternal blood at intervillous space. Consistent with previous reports, M・HLA-G was found expressed only in extravillous cytotrophoblasts. HLA-E was expressed weakly in synciciotrophoblasts and cytotrophoblasts and comparatively more strongly in extravillous cytotrophoblasts, essentially in parallel with total HLA-G. 2. Antigen presenting ability of HLA-G To investigate the ability, TAP dependency of HLA-G expression, and sequence of HLA-G bound peptide were examined. When HLA-G was isolated from transfected cells, a relatively large number of bound peptides derived from intra cellular proteins were identified, but the number of bound peptides was considerably smaller and the individual abundance considerably higher, with a single peptide species accounting for 15% of the total peptide bound to HLA-G from the placenta.
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