| Project/Area Number |
10670457
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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 |
Gastroenterology
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| Research Institution | NIIGATA UNIVERSITY |
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Principal Investigator |
NARISAWA Rintaro School of Medicine, NIIGATA UNIVERSITY Lecturer, 医学部, 講師 (30180540)
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| Co-Investigator(Kenkyū-buntansha) |
SUZUKI Kenji School of Medicine, NIIGATA UNIVERSITY Assistant, 医学部, 助手 (00303123)
ASAKURA Hitoshi School of Medicine, NIIGATA UNIVERSITY Professor, 医学部, 教授 (20051451)
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| Project Period (FY) |
1998 – 1999
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| Project Status |
Completed (Fiscal Year 1999)
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| Budget Amount *help |
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1999: ¥1,100,000 (Direct Cost: ¥1,100,000)
Fiscal Year 1998: ¥1,900,000 (Direct Cost: ¥1,900,000)
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| Keywords | Ulcerative colitis / Experimental colitis / Murine AIDS / Murine leukemia virus LP-BM5 / Sjoegren's syndrome / Macrophage / Cytokine / LP-BM5マウス白血病ウイルス / 炎症性腸疾患 / 漬瘍性大腸炎 / 動物モデル / B6ヌードマウス |
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| Research Abstract |
BACKGROUND : LP-BM5 murine leukemia virus (MuLV) is known to induce murine AIDS (MAIDS). We have shown that sjogren's syndrome (SjS) -like exocrinopathy can be induced in mice with MAIDS and that adoptive transfer of spleen cells from MAIDS mice can induce inflammatory bowel disease-like colitis as well as SjS-like exocrinopathy in nude mice. AIM : To assess the role of interferon (IFN)-g and interleukin (IL)-10 in the pathogenesis of our experimental model, we tried to identify the cells producing these cytokines and their localization in the colitis lesions in situ. METHODS : Four-week-old C57BL/6 (B6) mice were inoculated intraperitoneally with LP-BM5 MuLV.Eight weeks after infection, lymph node cells prepared from the virus-infected mice were transferred to B6 nude mice. Four to six weeks after the cell transfer, mice with clinical symptoms such as diarrhea, anal bleeding and body weight loss were killed to examine their colons. Expression of mRNA for IFN-g and IL-10 was assessed b
… More
y RTPCR, and protein expression of these cytokines was also analyzed in frozen sections of colon by double color-staining immunofluorescence (IF). RESULTS : All of the mice inoculated with MAIDS lymph node cells showed colitis as well as systemic exocrinopathy, and died within 6 weeks after cell transfer. Scattered erosions of the colon were observed. CD4+ cells were dominant and distributed diffusely within the mucosal and submucosal layers. A few CD8+ cells were detected among the intraepithelial lymphocytes of the colon. Mac-1+ cells were usually localized diffusely within the lamina propria and characteristically detected beneath the injured epithelial cells. B220+cells were localized within lymph follicles. An increase of IFN- g and IL-10 mRNA was detected in the colon of mice with colitis, but not in that of control mice. Double color IF showed that Mac-1+ cells were positive for IFN-g or IL-10 and that most CD4+ cells were positive for IL-10, although the population of IFN-g-positive CD4+ cells was low.
CONCLUSIONS : In our experimental colitis model, Mac-1+ macrophages which produce both IFN-g and IL-10 might play a crucial role in the pathogenesis of colitis in combination with CD4+ T cells. Less
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