| Project/Area Number |
17591764
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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 |
Obstetrics and gynecology
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| Research Institution | Hyogo College of Medicine |
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Principal Investigator |
HASHIMOTO Tomoko Hyogo College of Medicine, Faculty of Medicine, Professor (10172868)
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| Co-Investigator(Kenkyū-buntansha) |
MORINAGA Tomonori Hyogo College of Medicine, Faculty of Medicine, Research Associate (10351818)
KASIWAMURA Shinitiro Hyogo College of Medicine, Faculty of Medicine, Assistant Professor (00185761)
UEDA Haruyasu Hyogo College of Medicine, Faculty of Medicine, Assistant Professor (10330458)
OKAMURA Haruki Hyogo College of Medicine, Faculty of Medicine, Professor (60111043)
TUJI Yoshiyuki Hyogo College of Medicine, Faculty of Medicine, Part-time Assistant Professor (60148658)
谷澤 隆邦 兵庫医科大学, 医学部, 教授 (10126534)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2005: ¥2,200,000 (Direct Cost: ¥2,200,000)
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| Keywords | IL-18 / endothelial cells / stem cells / toll-like receptor / cDNA microarray / 未熟児 / 脳性麻痺 / 臍帯血 / 敗血症 / TGF-β |
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| Research Abstract |
We found that IL-18 in cord blood serves as a biochemical marker of brain damages followed by cerebral palsy in premature infants, and sepsis is another factor to induce neonatal brain damages. We examined the effects of IL-18 and endotoxin LPS, one of the toll-like receptor(TLR) ligands, to human immature endothelial cells. The cDNA microarray analysis showed that the expression of several chemokine and receptor genes and the endometrial bleeding associated factor gene, also known as Lefty-A, was induced by LPS. Lefty A was highly induced by IL-18 in one cell line but moderately in the other. We also used CD34-positive human hair follicle-derived stem cells that can differentiate to keratinocytes and neuronal cells. LPS induced the expression of Lefty A, IL8R and IL5RA, and IL-18 enhanced the expression of several chemokines. By treatment with other TLR ligands, the expression of the chomokine family and the ICAM genes were induced at a constant level, but the expression levels of IL-18 were variable among cell strains.
Recently, several reports noted that DNA polymorphisms vary clinical manifestations of severe infection. Taken together, in premature infants, severe infection and high serum IL-18 may cause damages to immature cells probably through TLR-mediated signals, and DNA polymorphisms may play an important role to modify the sensitivity to the signals.
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