van der Meer Werner J, van Steen Abraham C I, Mahlandt Eike, Rolas Loïc, Wang Haitao, Arts Janine J G, Kempers Lanette, Grönloh Max L B, Schoon Rianne M, Driessen Amber, van Rijssel Jos, Klaassen Ingeborg, Schlingemann Reinier O, Manavski Yosif, Hoogenboezem Mark, Boon Reinier A, Khuon Satya, Wait Eric, Heddleston John, Chew Teng-Leong, Nolte Martijn A, Nourshargh Sussan, Goedhart Joachim, van Buul Jaap D
Vascular 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.
Molecular Cell Biology Lab, Department of Molecular Hematology, Sanquin Research, and Landsteiner Laboratory, Amsterdam, the Netherlands.
Cell Rep. 2025 Sep 23;44(9):116242. doi: 10.1016/j.celrep.2025.116242. Epub 2025 Sep 4.
Upon inflammation, leukocytes extravasate through endothelial cells. When they extravasate, it is generally accepted that neighboring endothelial cells disconnect. Careful examination of endothelial junctions showed a partial membrane overlap beyond VE-cadherin distribution. These overlaps are regulated by actin polymerization and, although marked by, do not require PECAM-1, nor VE-cadherin. Neutrophils prefer wider membrane overlaps as exit sites. Detailed 3D analysis of neutrophil transmigration in real time at high spatiotemporal resolution revealed that overlapping endothelial membranes form a tunnel during neutrophil transmigration. These tunnels are formed by the neutrophil lifting the membrane of the upper endothelial cell while indenting and crawling over the membrane of the underlying endothelial cell. Our work shows that endothelial cells do not simply retract upon the passage of neutrophils but provide membrane tunnels, allowing neutrophils to extravasate. This discovery defines the 3D multicellular architecture in which the paracellular transmigration of neutrophils occurs.
在炎症发生时,白细胞通过内皮细胞渗出。当它们渗出时,普遍认为相邻的内皮细胞会分离。对内皮连接的仔细检查显示,在血管内皮钙黏蛋白分布之外存在部分膜重叠。这些重叠由肌动蛋白聚合调节,并且虽然以血小板内皮细胞黏附分子-1(PECAM-1)或血管内皮钙黏蛋白为标记,但并不需要它们。中性粒细胞更喜欢更宽的膜重叠作为出口位点。在高时空分辨率下对中性粒细胞迁移进行详细的实时三维分析发现,重叠的内皮膜在中性粒细胞迁移过程中形成一条隧道。这些隧道是由中性粒细胞抬起上层内皮细胞的膜,同时在下层内皮细胞的膜上凹陷并爬行而形成的。我们的研究表明,内皮细胞并非在中性粒细胞通过时简单地回缩,而是提供膜隧道,使中性粒细胞能够渗出。这一发现定义了中性粒细胞发生跨细胞旁迁移的三维多细胞结构。