ELUCIDATION OF MAKING ATRETIC FOLLICLES VIA APOPTOSIS AND MECHANISM OF INTRACELLULAR APOPTOTIC SIGNALS
Project/Area Number |
11671595
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Obstetrics and gynecology
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Research Institution | YAMAGATA UNIVERSITY |
Principal Investigator |
NAKAHARA Kenji YAMAGATA UNIV., OB/GYN, ASSISTANT PROFESSOR, 医学部, 講師 (80250934)
|
Co-Investigator(Kenkyū-buntansha) |
TANAKA Eiichi YAMAGATA UNIV., OB/GYN, ASSISTANT, 医学部, 助手 (20322000)
|
Project Period (FY) |
1999 – 2000
|
Project Status |
Completed (Fiscal Year 2000)
|
Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2000: ¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1999: ¥1,700,000 (Direct Cost: ¥1,700,000)
|
Keywords | APOPTOSIS / OVARY / ATRESIA OF FOLLICLE / GRANULOSA CELL / INTRACELLULAR SIGNAL TRANSDUCTION |
Research Abstract |
Fas-Fas ligand which is a system of signal transduction of apoptosis was used for elucidation of apoptotic system in ovaries from preovulatory female mice (B6C3 strain). Fas antigen is on the surface of granulosa cell membrane. Intracellular signal transduction starts after Fas ligand combines to Fas antigen. Fas antigen was not found on the surface of oocyte even in the atretic follicle of mouse. Otherwhile Fas antigen and Fas ligand was found on the surface of granulosa cells. In situ hybridization showed that apoptotic granulosa cells producted Fas antigen and not Fas ligand. Fas ligands was producted in oocyte. Therefore oocytes hold the key to follicle development or atretic follicles. Protein C kinase mediates intracellular signal transduction of granulosa cells. Other signal transduction was suggested while blockage of intracellular transduction via protein C kinase was no use in follicle development. Further investigation is necessary for detection of all of intracellular signal transduction for apoptosis in atretic follicles.
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Report
(3 results)
Research Products
(12 results)