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骨制御分子Runx2による中枢制御機構の解明
https://doi.org/10.24517/00050080
https://doi.org/10.24517/00050080fd85d76f-8cc4-4293-9e66-b345086c6f14
名前 / ファイル | ライセンス | アクション |
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PH-PR-TAKARADA-T-kaken 2013-4p.pdf (367.0 kB)
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Item type | 報告書 / Research Paper(1) | |||||
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公開日 | 2018-02-09 | |||||
タイトル | ||||||
タイトル | 骨制御分子Runx2による中枢制御機構の解明 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Regulatory mechanisms of central nervous system by Runx2 | |||||
言語 | ||||||
言語 | jpn | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_18ws | |||||
資源タイプ | research report | |||||
ID登録 | ||||||
ID登録 | 10.24517/00050080 | |||||
ID登録タイプ | JaLC | |||||
著者別表示 |
Takarada, Takeshi
× Takarada, Takeshi |
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提供者所属 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 金沢大学医薬保健研究域薬学系 | |||||
書誌情報 |
平成24(2012)年度 科学研究費補助金 基盤研究(C) 研究成果報告書 en : 2012 Fiscal Year Final Research Report 巻 2010-2012, p. 4p., 発行日 2013-05-23 |
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出版者 | ||||||
出版者 | 金沢大学医薬保健研究域薬学系 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | 我々は、骨芽細胞特異的表現型を特徴付けるRunt-related transcription factor 2(Runx2)分子が、中枢神経系にも機能的に発現する事実を報告した。本研究では、個体レベルでのRunx2の脳機能解析を実施する目的で、Cre/loxPシステムを利用したRunx2 conditional欠損マウスの作製に取り組み、Runx2遺伝子のexon 4をloxP配列にて挟んだRunx2^flox/+のマウス作製に成功した。 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | We have previously shown the functional expression of glutamatergic and GABAergic signaling machineries in different osseous cells including osteoblasts. Runt-related factor 2 (Runx2) is the master regulator of osteoblastic differentiation with ability to accelerate differentiation of mesenchymal stem cells into osteoblasts, while we have also demonstrated the expression of mRNA and corresponding protein for Runx2. In this study, we for the first time generated mice carrying a conditional Runx2 allele with exon 4, which encodes the Runt domain, flanked by loxP sites. These mice were crossed with α1(I)-collagen-Cre or α1(II)-collagen-Cre transgenic mice to obtain osteoblast- or chondrocyte-specific Runx2 deficient mice, respectively. In newborn α1(II)-Cre;Runx2^flox/flox mice, mineralization impairment was restricted to skeletal areas undergoing endochondral ossification including long bones and vertebrae. In contrast, no apparent skeletal abnormalities were seen in mutant embryo, newborn, and 3- to 6-week old-mice in which Runx2 had been deleted with the α1(I)-collagen-Cre driver. The Runx2 floxed allele established here is undoubtedly useful for investigating the role of Runx2 in particular cells. | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 研究課題/領域番号:22500330, 研究期間(年度):2010-2012 | |||||
内容記述 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 出典:研究課題「骨制御分子Runx2による中枢制御機構の解明」課題番号22500330 (KAKEN:科学研究費助成事業データベース(国立情報学研究所)) (https://kaken.nii.ac.jp/report/KAKENHI-PROJECT-22500330/22500330seika/)を加工して作成 |
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著者版フラグ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://kaken.nii.ac.jp/search/?qm=30377428 | |||||
関連名称 | https://kaken.nii.ac.jp/search/?qm=30377428 | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-22500330/ | |||||
関連名称 | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-22500330/ | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://kaken.nii.ac.jp/report/KAKENHI-PROJECT-22500330/22500330seika/ | |||||
関連名称 | https://kaken.nii.ac.jp/report/KAKENHI-PROJECT-22500330/22500330seika/ |