白血球は内皮膜のトンネルを使って血管系を外流させる
Werner J van der Meer1, Abraham C I van Steen2, Eike Mahlandt3
1Vascular Cell Biology Lab, Department of Medical Biochemistry, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands; Molecular Cell Biology Lab, Department of Molecular Hematology, Sanquin Research, and Landsteiner Laboratory, Amsterdam, the Netherlands.
Cell reports
|September 6, 2025
まとめ
内皮細胞は,中性粒子の放出時に膜のトンネルを形成し,切り離さない. 中性粒子はこれらのアクチン調節されたトンネルを利用し,白血球の転移のための新しい3Dアーキテクチャを明らかにします.
科学分野:
- 細胞生物学
- 免疫学
- バイオ物理学
背景:
- 白血球の放出は 免疫反応に不可欠です
- 以前は,転移時に内皮細胞の接続が完全に切断されると考えられていた.
研究 の 目的:
- 中性粒子の転移中の内皮細胞の3D構造を調査する.
- 白血球外流における内皮細胞の相互作用の役割を明らかにする.
主な方法:
- 高解像度3Dライブ画像
- 内皮細胞の結合ダイナミクスの分析
- アクチンポリメリゼーション,PECAM-1,およびVE-カデリンの役割を調査した.
主要な成果:
- 内皮細胞は,VE-カデリンを超えて部分的な膜の重なりを示します.
- アクチンポリメリゼーションはこれらの重複を調節し,PECAM-1またはVE-カデリンを必要としません.
- 中性粒子は,転移のために内皮細胞の重なりによって形成された膜のトンネルを作り,それを利用する.
結論:
- 内皮細胞は,中性粒子の通過を容易にするため,膜のトンネルを積極的に形成します.
- これは単純な内皮細胞の断絶という概念に 異議を唱えます
- パラセル移動のための新しい3D多細胞構造を定義します.
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