The transport mechanism of the lactate transporter between Sertoli cells and spermatocytes and the role of seminolipid in it.
Project/Area Number |
16K08591
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General medical chemistry
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Research Institution | Kochi University |
Principal Investigator |
Honke Koichi 高知大学, その他部局等, 副学長 (80190263)
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Project Period (FY) |
2016-04-01 – 2019-03-31
|
Project Status |
Completed (Fiscal Year 2018)
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Budget Amount *help |
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2018: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2017: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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Keywords | 精子形成 / 精母細胞 / セルトリ細胞 / セミノリピド / 乳酸 / MCT4 / ベイシジン / 細胞外小胞 / 乳酸トランスポーター / 発生・分化 / 生体分子 / 糖鎖 / 脂質 |
Outline of Final Research Achievements |
We have elucidated the molecular function of seminolipid, which is the sulfated glycolipid specifically expressed in mammalian testes. Since the testis has the blood-testis barrier, spermatocytes utilize lactate that is produced from glucose in Sertoli cells as the energy source. We found that the lactate transporter on the plasm membrane of spermatocytes is MCT4 and it can function only after it forms assembly with basigin. After the MCT4 gene is transcribed and translated in Sertoli cells, MCT4 proteins are found to be secreted into the extracellular vesicles and transported to spermatocytes. We found that this secretion of the extracellular vesicles from Sertoli cells is stimulated by seminolipid.
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Academic Significance and Societal Importance of the Research Achievements |
男性不妊の多くは精子形成障害が原因である。哺乳動物の精子形成は精巣中で起こるが、精子形成細胞と支持細胞のセルトリ細胞の相互作用で進行する。精子形成細胞は2回減数分裂を行い、半数体の精子になる。セミノリピドを欠損したマウスは、第一減数分裂の途中で停止し不妊となることから、精子形成に必須の分子であることがわかっているが、その分子メカニズムは不明であった。本研究によってその分子メカニズムが明らかとなった。本研究により、セルトリ細胞と精子形成細胞間のコミュニケーションに細胞外小胞が使われていることが明らかとなった。正常の発生過程においても細胞外小胞の重要性が明確となった。
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Report
(3 results)
Research Products
(14 results)
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[Journal Article] Analysis of lipid raft molecules in the living brain slices2018
Author(s)
Kotani N, Nakano T, Ida Y, Ito R, Hashizume M, Yamaguchi A, Seo M, Araki T, Hojo Y, Honke K, Murakoshi T
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Journal Title
Neurochemistry International
Volume: 119
Pages: 140-150
DOI
Related Report
Peer Reviewed
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[Journal Article] ASC amino acid transporter 2, defined by enzyme-mediated activation of radical sources, enhances malignancy of GD2-positive small-cell lung cancer.2018
Author(s)
Nobutoshi Esaki, Yuki Ohkawa, Noboru Hashimoto, Yuhsuke Tsuda, Yuhsuke Ohmi, Robiul H. Bhuiyan, Norihiro Kotani, Koichi Honke, Atsushi Enomoto, Masahide Takahashi, Keiko Furukawa, Koichi Furukawa.
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Journal Title
Cancer Scienc
Volume: 109
Pages: 141-153
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] 1.Imamaki R. Ogawa K, Kizuka Y, Komi Y, Kojima S, Kotani N, Honke K, Honda T, Taniguchi N, and Kitazume S2018
Author(s)
1.Imamaki R. Ogawa K, Kizuka Y, Komi Y, Kojima S, Kotani N, Honke K, Honda T, Taniguchi N, and Kitazume S
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Journal Title
Oncogene
Volume: -
Pages: 4287-4299
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Ganglioside GD3 enhances invasiveness via Yes activation by forming a complex of GD3/PDGFRα/Yes in gliomas2016
Author(s)
Yuki Ohkawa, Hiroyuki Momota, Akira Kato, Noboru Hashimoto, Yuhsuke Tsuda, Norihiro Kotani, Koichi Honke, Akio Suzumura, Keiko Furukawa, Yuhsuke Ohmi, Atsushi Natsume, Toshihiko Wakabayashi and *Furukawa K
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Journal Title
Journal of Biological Chemistry
Volume: 290
Pages: 16043-16058
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
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