Pulmonary, Allergy and Critical Care Division, Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Cell Adh Migr. 2011 Jan-Feb;5(1):37-41. doi: 10.4161/cam.5.1.13575. Epub 2011 Jan 1.
Filopodia are an important feature of actively motile cells, probing the pericellular environment for chemotactic factors and other molecular cues that enable and direct the movement of the cell. They also act as points of attachment to the extracellular matrix for the cell, generating tension that may act to pull the cell forward and/or stabilize the cell as it moves. Endothelial cell motility is a critical aspect of angiogenesis, but only a limited number of molecules have been identified as specific regulators of endothelial cell filopodia. Recent reports, however, provide evidence for the involvement of PECAM-1, an endothelial cell adhesion and signaling molecule, in the formation of endothelial cell filopodia. This commentary will focus on these studies and their suggestion that at least two PECAM-1-regulated pathways are involved in the processes that enable filopodial protrusions by endothelial cells. Developing a more complete understanding of the role of PECAM-1 in mediating various endothelial cell activities, such as the extension of filopodia, will be essential for exploiting the therapeutic potential of targeting PECAM-1.
丝状伪足是活跃运动细胞的一个重要特征,它们可以探测细胞周围环境中的趋化因子和其他分子线索,从而使细胞能够移动并为其移动提供指导。它们还充当细胞与细胞外基质的附着点,产生的张力可以拉动细胞向前移动和/或稳定细胞在移动时的状态。内皮细胞的运动是血管生成的一个关键方面,但只有少数分子被确定为内皮细胞丝状伪足的特异性调节因子。然而,最近的报告提供了证据,表明内皮细胞黏附与信号分子PECAM-1参与了内皮细胞丝状伪足的形成。本评论将重点介绍这些研究及其表明至少有两种 PECAM-1 调节途径参与了使内皮细胞丝状伪足伸出的过程。更全面地了解 PECAM-1 在介导各种内皮细胞活动(如丝状伪足的延伸)中的作用,对于利用靶向 PECAM-1 的治疗潜力至关重要。