CD27/CD70 interactions in B cell immunoglobulin production
| Project/Area Number |
07670854
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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 |
Pediatrics
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| Research Institution | Dept.of Pediatr., Shinshu Univ.Sch.of Med. |
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Principal Investigator |
AGEMATSU Kazunaga Dept.Pediatr.Shinshu Univ.Sch.of Med., Asistant Prof., 医学部附属病院, 講師 (60262721)
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| Project Period (FY) |
1995 – 1997
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| Project Status |
Completed (Fiscal Year 1997)
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| Budget Amount *help |
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1997: ¥300,000 (Direct Cost: ¥300,000)
Fiscal Year 1996: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1995: ¥900,000 (Direct Cost: ¥900,000)
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| Keywords | Plasma cells / Memory B cells / CD27 / CD70 / Naive B cells / 免疫応答 / B細胞 / ヘルパーT細胞 / Immunoglolulin |
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| Research Abstract |
B cell immunoglobulin production is regulated by direct interaction and cytokines of helper T cells. In the present studies, wer had functionally analyzed CD27 in cord and peripheral blood B cells. Adult peripheral blood B cells were separated into CD27+ and CD27- cells, which were different in the morphology. Cord blood B cells did not express CD27, and CD27 expression on peripheral blood B cells increased with age in parallel. Only CD27+ B cells had ability to produce immunoglobulin, which was increased by contact with a TNF-related transmembrane ligand, CD70. Adult peripheral blood CD27+ B cells can be further subdivided into two discrete subtypes : IgD-CD27+ and IgD+CD27+B cells. IgD-CD27+B cells produced IgG,IgM and IgA,where as IgD+CD27+B cells predominantly produce IgM.The addition of activated CD4+CD45ROT cells with CD70 caused down-regulation of CD27 expression on activated B cells, and its down modulation was completely blocked by anti-CD70 mAb, indicating direct T-B cell con
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tact via CD27/CD70. The triggering via CD27 and CD40 additively increased the immunoglobulin production under SAC plus IL-2 stimulation.
The triggering via CD27 by CD27 ligand (CD70) on purified peripheral blood B cells yielded an increase in the number of plasma cells in the presence of interleukin-10 (IL-10). The differentiation into plasma cells by a combination of IL-10 and CD70-transfectants occurred in CD27+B cells, but not in CD27-B cells. Moreover, the addition of IL-2 to the IL-10 and CD70-transfect activation system greatly induced the differentiation into plasma cells. In the presence of only IL-2, IL-4 or IL-6, CD70-transfectants did not promote the differentiation into plasma cells. On the other hand, CD40 signaling increased the expansion of a B cell pool from peripheral blood B cells primarily activated by IL-2, IL-10 and anti-CD40 mAb. Finally, CD27 signaling also rescued B cells from IL-10-mediated apoptosis. Taken together, our findings demonstrate peripheral blood B cells are separated into subpopulations by CD27 and IgD expression and that CD27+B cells produce large amounts of immunoglobulin by the interaction with CD70 molecule. These data also demonstrate that CD27 ligand (CD70) is a key molecule to prevent the IL-10-mediated promotion of apoptosis and to direct the differentiation of CD27+memory B cells toward plasma cells in cooperation with IL-10. Less
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Report
(4 results)
Research Products
(11 results)
