Project/Area Number |
22591816
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Obstetrics and gynecology
|
Research Institution | Gunma University |
Principal Investigator |
ABE Yumiko 群馬大学, 保健学研究科, 准教授 (70261857)
|
Project Period (FY) |
2010-04-01 – 2014-03-31
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2013: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2010: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
|
Keywords | アクチビン / フォリスタチン / FIRS / 絨毛膜羊膜炎 / 羊膜細胞 / インヒビン |
Research Abstract |
Chorioamnionitis is the primary disease of FIRS. Because the amnion is the avascular tissue, activin A produced in the amniotic cells is directly secreted into amniotic fluid, and seems to affect the fetus. Using cultured human amniotic cells with LPS or TNF-alpha, as a model system of amnionitis, we clarified that these factors stimulate activin A secretion from amniotic cells. A biologically active form of activin A is free activin A, which is not bound by the binding proteins follistatin or FSTL3. Therefore, we synthesized a peptide which has an amino acid sequence of follistatin/FSTL3-binding site of activin A, used it in immunization and obtained antibodies. The antibodies were purified by immunochromatography. Using the antibodies, we are analyzing the activin A secreted from amniotic cells by the stimulation of TNF-alpha.
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