| Project/Area Number |
03670218
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
細菌学
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| Research Institution | Saga Medical School |
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Principal Investigator |
KOHASHI Osamu Saga Medical School, Microbiology, Professor, 医学部, 教授 (50112777)
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| Co-Investigator(Kenkyū-buntansha) |
KUKITA Akiko Saga Medical School, Microbiology, Assist.professor, 医学部, 助手 (30153266)
OHKI Kazunori Saga Medical School, Microbiology, Assist. professor, 医学部, 助手 (30128128)
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| Project Period (FY) |
1991 – 1992
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| Project Status |
Completed (Fiscal Year 1992)
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| Budget Amount *help |
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1992: ¥300,000 (Direct Cost: ¥300,000)
Fiscal Year 1991: ¥1,600,000 (Direct Cost: ¥1,600,000)
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| Keywords | Adjuvant-induced arthritis / Heat-shock 65 Kd protein / Macrophage cell lines / BCG / Osteoclast / 組換えDNA |
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| Research Abstract |
In order to know whether 65 KD heat-shock protein can suppress BCG-induced arthritis and MDP-induced arthritis in rats, the rats were pretreated with the heat-shock proteins, followed by injection of BCG or MDP. There was no significant pathogenic relationship of pretreatment of 65 Kd heat shock protein between arthritic rats and non-arthritic rats after injection of BCG or synthetic MDP, suggesting an unknown autoantigen(s) other than heat-shock protein in induction and propagation of autoimmune arthritis in rats. In view of an important role of macrophages involving in local inflammatory responses, we, thus studied the effect of macrophages on bone formation and bone resorption of local joint. We have established several macrophages strains. MDP and LPS stimulated the macrophages to produce several monokines which enhance the bone dystruction. One factor enhanced the induction of Osteoclast that was able to absorb the bone.
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