| Project/Area Number |
17K17690
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
General medical chemistry
Urology
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| Research Institution | Institute of Physical and Chemical Research (2018-2019)
Tokyo Medical and Dental University (2017) |
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Principal Investigator |
Takase Hinako M 国立研究開発法人理化学研究所, 生命機能科学研究センター, 研究員 (40754528)
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| Project Period (FY) |
2017-04-01 – 2020-03-31
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| Project Status |
Completed (Fiscal Year 2019)
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| Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2018: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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| Keywords | 精子形成 / Wntシグナル / 未分化型精原細胞 / Wnt / 精子幹細胞 / セルトリ細胞 / ライディッヒ細胞 / 発生・分化 / 生殖細胞 / Wntシグナル伝達経路 |
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| Outline of Final Research Achievements |
In this study, we tested the role of Sertoli and Leydig cell-derived Wnt in the regulation of undifferentiated spermatogonia. Genetically modified (Wls cKO) mice showed reduced testicular weight and abnormal spermatogenesis partially. In Wls cKO mice, no significant changes in undifferentiated spermatogonia were detected, while there was a reduction of differentiated spermatogonia. It is possible that Sertoli and Leidig cell-derived Wnt ligands may act on autocrine manner or myoid cells and to indirectly support spermatogenesis.
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| Academic Significance and Societal Importance of the Research Achievements |
精細管内唯一の体細胞であるセルトリ細胞は、全ての分化段階にある生殖細胞を物理的に支持すると同時に、未分化精原細胞の自己複製と分化を調節する。セルトリ細胞とライディッヒ細胞が産生するWntリガンドはが未分化精原細胞へ直接的に作用するという証拠は得られなかったが、その一方で、体細胞もしくは精巣網の機能維持に関与し、間接的に精子形成を支えることが示唆された。
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