
| ID | 69761 |
| フルテキストURL | |
| 著者 |
Moriya, Takumi
Department of Oral Morphology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Surong, A.
Department of Neuroscience, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Tatsumi, Nanami
Department of Neuroscience, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Yamada, Hiroshi
Department of Neuroscience, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kaken ID
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Takemoto, Fumiko
Department of Orthodontics, Okayama University Hospital
Kamioka, Hiroshi
Department of Orthodontics, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kaken ID
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Okamura, Hirohiko
Department of Oral Morphology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
ORCID
Kaken ID
publons
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Ikegame, Mika
Department of Oral Morphology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University
Kaken ID
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| 抄録 | Objectives: Dynamin, a GTPase that regulates membrane dynamics, has recently been implicated in actin cytoskeletal remodeling. This study aimed to elucidate the role of dynamin in osteoblast migration by examining the effects of dynamin inhibition on the localization and organization of F-actin and dynamin 2 in MC3T3-E1 cells.
Methods: MC3T3-E1 cells were treated with dynamin inhibitors (Dyngo 4a and Dynole 34-2), and cell migration was assessed using a wound-healing assay. Fluorescent staining was performed to analyze the intracellular localization of F-actin and dynamin 2. Results: Dynamin inhibition significantly reduced the migration of MC3T3-E1 cells. Fluorescence analysis revealed a marked decrease in the accumulation and colocalization of F-actin and dynamin 2 at the protrusion edge. Additionally, dynamin inhibition suppressed the formation of lamellipodia and stress fibers while promoting the appearance of abnormal F-actin clusters in the cytoplasm. Conclusions: These findings suggest that dynamin plays an essential role in osteoblast migration by regulating actin cytoskeletal remodeling, particularly through the formation of lamellipodia and stress fibers. |
| キーワード | Dynamin
Cell migration
Osteoblasts
F-actin
|
| 発行日 | 2026-02
|
| 出版物タイトル |
Journal of Oral Biosciences
|
| 巻 | 68巻
|
| 号 | 1号
|
| 出版者 | Elsevier BV
|
| 開始ページ | 100720
|
| ISSN | 1349-0079
|
| NCID | AA11896386
|
| 資料タイプ |
学術雑誌論文
|
| 言語 |
英語
|
| OAI-PMH Set |
岡山大学
|
| 著作権者 | © 2025 Japanese Association for Oral Biology.
|
| 論文のバージョン | publisher
|
| DOI | |
| 関連URL | isVersionOf https://doi.org/10.1016/j.job.2025.100720
|
| ライセンス | http://creativecommons.org/licenses/by/4.0/
|
| 助成情報 |
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( 文部科学省 / Ministry of Education )
21K19644:
母子健康に理想的な口腔環境を探る~歯周病原菌の小胞による胎盤組織への障害性~
( 文部科学省 / Ministry of Education )
22H06790:
( 文部科学省 / Ministry of Education )
24K23553:
機械的刺激が骨芽細胞の移動方向を制御するメカニズムの解明
( 文部科学省 / Ministry of Education )
JPJS00420230010:
( 独立行政法人日本学術振興会 / Japan Society for the Promotion of Science )
|