Department of Pathology, School of Medical Sciences, University of New South Wales, Sydney, Australia.
Institut National de la Santé et de la Recherche Médicale U1170, Gustave Roussy Institute, Université Paris-Saclay, Villejuif, France.
J Cell Biol. 2019 Jul 1;218(7):2086-2095. doi: 10.1083/jcb.201811160. Epub 2019 Jun 17.
An understanding of the mechanisms whereby cell adhesion complexes (ACs) relay signals bidirectionally across the plasma membrane is necessary to interpret the role of adhesion in regulating migration, differentiation, and growth. A range of AC types has been defined, but to date all have similar compositions and are dependent on a connection to the actin cytoskeleton. Recently, a new class of AC has been reported that normally lacks association with both the cytoskeleton and integrin-associated adhesome components, but is rich in components of the clathrin-mediated endocytosis machinery. The characterization of this new type of adhesion structure, which is emphasized by mitotic cells and cells in long-term culture, identifies a hitherto underappreciated link between the adhesion machinery and clathrin structures at the plasma membrane. While this discovery has implications for how ACs are assembled and disassembled, it raises many other issues. Consequently, to increase awareness within the field, and stimulate research, we explore a number of the most significant questions below.
要理解细胞黏附复合物 (ACs) 如何在质膜两侧双向传递信号,就必须解释黏附在调节迁移、分化和生长中的作用。已经定义了一系列的 AC 类型,但迄今为止,它们都具有相似的组成,并依赖于与肌动蛋白细胞骨架的连接。最近,报道了一种新型的 AC,它通常与细胞骨架和整合素相关黏着斑成分都没有关联,但富含网格蛋白介导的内吞作用机制的成分。这种新型黏附结构的特征在有丝分裂细胞和长期培养的细胞中尤为明显,它在黏附机制和质膜网格蛋白结构之间建立了一个迄今为止尚未被充分认识的联系。虽然这一发现对 AC 的组装和拆卸方式有影响,但它也提出了许多其他问题。因此,为了提高该领域的认识,并激发研究,我们探讨了以下一些最重要的问题。