このアイテムのアクセス数: 105
このアイテムのファイル:
ファイル | 記述 | サイズ | フォーマット | |
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j.celrep.2021.109550.pdf | 5.56 MB | Adobe PDF | 見る/開く |
完全メタデータレコード
DCフィールド | 値 | 言語 |
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dc.contributor.author | Mori, Yoshifumi | en |
dc.contributor.author | Takashima, Seiji | en |
dc.contributor.author | Kanatsu-Shinohara, Mito | en |
dc.contributor.author | Yi, Zheng | en |
dc.contributor.author | Shinohara, Takashi | ja |
dc.contributor.alternative | 森, 圭史 | ja |
dc.contributor.alternative | 高島, 誠司 | ja |
dc.contributor.alternative | 篠原, 美都 | ja |
dc.contributor.alternative | 篠原, 隆司 | ja |
dc.date.accessioned | 2021-08-31T05:50:47Z | - |
dc.date.available | 2021-08-31T05:50:47Z | - |
dc.date.issued | 2021-08 | - |
dc.identifier.uri | http://hdl.handle.net/2433/265005 | - |
dc.description | 精子形成促進分子GDNFの制御機構の解明 --男性不妊治療への応用に期待--. 京都大学プレスリリース. 2021-08-19. | ja |
dc.description.abstract | Spermatogonial stem cells (SSCs) are maintained in a special microenvironment called a niche. However, much is unknown about components that constitute the niche. Here, we report that Cdc42 is essential for germline niche development. Sertoli cell-specific Cdc42-deficient mice showed normal premeiotic spermatogenesis. However, germ cells gradually disappeared during haploid cell formation and few germ cells remained in the mature testes. Spermatogonial transplantation experiments revealed a significant loss of SSCs in Cdc42-deficient testes. Moreover, Cdc42 deficiency in Sertoli cells downregulated GDNF, a critical factor for SSC maintenance. Cdc42-deficient Sertoli cells also exhibited lower nuclear MAPK1/3 staining. Inhibition of MAP2K1 or depletion of Pea15a scaffold protein downregulated GDNF expression. A screen of transcription factors revealed that Cdc42-deficient Sertoli cells downregulate DMRT1 and SOX9, both of which are critical for Sertoli cell development. These results indicate that Cdc42 is essential for niche function via MAPK1/3-dependent GDNF secretion. | en |
dc.language.iso | eng | - |
dc.publisher | Elsevier BV | en |
dc.rights | © 2021 The Author(s). | en |
dc.rights | This is an open access article under the Creative Commons Attribution 4.0 International. | en |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | CDC42 | en |
dc.subject | GDNF | en |
dc.subject | MAP2K1 | en |
dc.subject | DMRT1 | en |
dc.subject | SOX9 | en |
dc.subject | spermaogonial stem cells | en |
dc.subject | niche | en |
dc.title | Cdc42 is required for male germline niche development in mice | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Cell Reports | en |
dc.identifier.volume | 36 | - |
dc.identifier.issue | 7 | - |
dc.relation.doi | 10.1016/j.celrep.2021.109550 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | 109550 | - |
dc.address | Department of Molecular Genetics, Graduate School of Medicine, Kyoto University; Present address: Kyoen Cosmetic Surgery and Clinique | en |
dc.address | Department of Molecular Genetics, Graduate School of Medicine, Kyoto University; Present address: Department of Textile Science and Technology, Interdisciplinary Graduate School of Science and Technology, Shinshu University | en |
dc.address | Department of Molecular Genetics, Graduate School of Medicine, Kyoto University; AMED-CREST | en |
dc.address | Division of Experimental Hematology, Molecular Developmental Biology Graduate Program, Children’s Hospital Research Foundation, University of Cincinnati | en |
dc.address | Department of Molecular Genetics, Graduate School of Medicine, Kyoto University | en |
dc.identifier.pmid | 34407418 | - |
dc.relation.url | https://www.kyoto-u.ac.jp/ja/research-news/2021-08-19 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 19K22512 | - |
datacite.awardNumber | 19H05750 | - |
datacite.awardNumber | 19H04906 | - |
datacite.awardNumber | 18H04882 | - |
datacite.awardNumber | 18H05281 | - |
datacite.awardNumber | 18H02935 | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/ja/grant/KAKENHI-PROJECT-19K22512/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/ja/grant/KAKENHI-PLANNED-19H05750/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/ja/grant/KAKENHI-PUBLICLY-19H04906/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/ja/grant/KAKENHI-PUBLICLY-18H04882/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18H05281/ | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18H02935/ | - |
dc.identifier.pissn | 2211-1247 | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.awardTitle | ヒト精子幹細胞の機能解析および培養系確立 | ja |
jpcoar.awardTitle | 受精卵全能性を統御する遺伝子群の単離と機能解析 | ja |
jpcoar.awardTitle | 精子幹細胞に由来する子孫が行動様式に及ぼす影響 | ja |
jpcoar.awardTitle | 性決定に関わる抑制性ヒストン修飾の役割 | ja |
jpcoar.awardTitle | 精子幹細胞のアンチエイジング機構の解明 | ja |
jpcoar.awardTitle | ヒト精子幹細胞の長期培養系の確立 | ja |
出現コレクション: | 学術雑誌掲載論文等 |

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