| Project/Area Number |
07457385
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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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 | KYOTO UNIVERSITY |
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Principal Investigator |
MORI Takahide Dept.of Gynecology and Obstetrics, Faculty of Medicine, Professor, 医学研究科, 教授 (90026865)
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| Co-Investigator(Kenkyū-buntansha) |
FUJIWARA Hiroshi Dept.of Gyn/Ob, Faculty of Medicine, Associate Professor, 医学研究科, 講師 (30252456)
今井 公俊 京都大学, 医学研究科, 助手 (90252436)
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥6,800,000 (Direct Cost: ¥6,800,000)
Fiscal Year 1996: ¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1995: ¥3,800,000 (Direct Cost: ¥3,800,000)
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| Keywords | monoclonal antibody / corppus luteum / luteal cells / differenttiation / gonadotropin / cytokine / integrin / extracellular matrix / 分化抗原 / 抗原精製 / アミノ酸シークエンス |
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| Research Abstract |
Summary of Research Results
Corpus luteum (CL) has important physiological functions in the female reproduction. It is generally accepted that corpus luteum is essential for successful pregnancy. Luteal dysfunction is assumed to be one of causes of infertility and/or habitual abortion.In addition, it is suggested that luteal insufficiency may cause endometrial hyperplasia and cancer. Furthermore, during the luteal phase, luteal cells show morphological and functional changes. During the CL formation, follicular cells differentiate to luteal cells, and steroidogenic enzymes are induced to produce progesterone and so on. During the CL regression, luteal cells demonstrate apoptotic changes. Therefore, luteal cells are useful materials for analysis of cell differentiation. However, differentiation of luteal cells are not understood, to date.
To investigate the differentiation pathways and regulatory mechanisms of differentiation of human luteal cells in the ovary, we raised murine monoclonal
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antibodies (mAbs) against human luteal cells, and analyzed the cell-lineage-and differentiation stage-specifically expressed molecules on cell surface. (1) We have obtained several mAbs that recognize granulosa cell lineage-specific or thecal cell lineage-specific cell surface molecules. From these data, we proposed the human granulosa cells differentiate to large luteal cells of the menstrual CL and also CL of early pregnancy, and that human theca interna cells differentiate to small luteal cells. (2) We have found expression profiles of several molecules are different between the menstrual CL and CL of pregnancy. This suggest that CL of pregnancy have different functions from CL of the cycle. (3) Though the study on the effect of gonadotropins and cytokines on the expression of the differentiation-related antigens on luteal cells, we have found that differentiation of luteal cells are regulated not only by gonadotropins but also by cytokines. This suggests that immunological factors are involved in the differentiation of menstrual CL to CL of pregnancy. (4) We have found that the interaction between integrins (cell adhesion molecules) and extracellular matrices are local regulator of the differentiation of luteal cells. Less
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