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ID 69761
フルテキストURL
fulltext.pdf 5.02 MB
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 publons researchmap
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 publons researchmap
Okamura, Hirohiko Department of Oral Morphology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University ORCID Kaken ID publons researchmap
Ikegame, Mika Department of Oral Morphology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Kaken ID publons researchmap
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
68巻
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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22H03511: 歯周病が胎盤・胎児の成長発育を阻害する分子メカニズムの解明 ( 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 )