Ren Gang, Crampton Matthew S, Yap Alpha S
Institute for Molecular Bioscience, Division of Molecular Cell Biology, The University of Queensland, St. Lucia, Brisbane, Queensland, Australia 4072.
Cell Motil Cytoskeleton. 2009 Oct;66(10):865-73. doi: 10.1002/cm.20380.
It has long been recognized that adhesion receptors cooperate with the cytoskeleton during morphogenesis, tissue remodeling and homeostasis. But how this occurs is less well-understood. A host of cytoskeletal regulators have been reported to have functional and biochemical linkage with adhesion receptors. The challenge remains to find functionally-coherent patterns within this increasingly large corpus of molecular information. In this review we discuss one approach, to identify distinctive functional modules that contribute to different adhesive processes. We illustrate this by considering Arp2/3-driven surface protrusion, which is utilized at both integrin-based cell-matrix adhesions and cadherin-based cell-cell adhesions. We further argue that regulatory proteins, such as cortactin, serve to coordinate the molecular components of this protrusive apparatus into a cohesive module.
长期以来,人们已经认识到粘附受体在形态发生、组织重塑和体内平衡过程中与细胞骨架协同作用。但具体的发生机制尚不清楚。据报道,许多细胞骨架调节因子与粘附受体存在功能和生化联系。在这一数量日益庞大的分子信息库中,找出功能上连贯的模式仍是一项挑战。在本综述中,我们讨论了一种方法,即识别有助于不同粘附过程的独特功能模块。我们通过研究由Arp2/3驱动的表面突起来说明这一点,这种突起在基于整合素的细胞-基质粘附和基于钙粘蛋白的细胞-细胞粘附中均有应用。我们进一步认为,诸如皮层肌动蛋白等调节蛋白有助于将这种突出装置的分子成分协调成一个有凝聚力的模块。