Löster K, Vossmeyer D, Hofmann W, Reutter W, Danker K
Institut für Molekularbiologie und Biochemie, Freie Universität Berlin, Arnimallee 22, D-14195 Berlin-Dahlem, Germany.
Biochem J. 2001 May 15;356(Pt 1):233-40. doi: 10.1042/0264-6021:3560233.
Integrins are heterodimeric adhesion receptors consisting of alpha- and beta-subunits capable of binding extracellular matrix molecules as well as other adhesion receptors on neighbouring cells. These interactions induce various signal transduction pathways in many cell types, leading to cytoskeletal reorganization, phosphorylation and induction of gene expression. Integrin ligation leads to cytoplasmic protein-protein interactions requiring both integrin cytoplasmic domains, and these domains are initiation points for focal adhesion formation and subsequent signal transduction cascades. In previous studies we have shown that the very short cytoplasmic alpha1 tail is required for post-ligand events, such as cell spreading as well as actin stress-fibre formation. In the present paper we report that cells lacking the cytoplasmic domain of the alpha1 integrin subunit are unable to form proper focal adhesions and that phosphorylation on tyrosine residues of focal adhesion components is reduced on alpha1beta1-specific substrates. The alpha1 cytoplasmic sequence is a specific recognition site for focal adhesion components like paxillin, talin, alpha-actinin and pp125FAK. It seems to account for alpha1-specific signalling, since when peptides that mimic the cytoplasmic domain of alpha1 are transferred into cells, they influence alpha1beta1-specific adhesion, presumably by competing for binding partners. For alpha1 integrin/protein binding, the conserved Lys-Ile-Gly-Phe-Phe-Lys-Arg motif and, in particular, the two lysine residues, are important.
整合素是由α亚基和β亚基组成的异二聚体黏附受体,能够结合细胞外基质分子以及相邻细胞上的其他黏附受体。这些相互作用在许多细胞类型中诱导各种信号转导途径,导致细胞骨架重组、磷酸化以及基因表达的诱导。整合素连接导致需要两个整合素胞质结构域的胞质蛋白-蛋白相互作用,并且这些结构域是粘着斑形成和随后信号转导级联反应的起始点。在先前的研究中,我们已经表明,非常短的胞质α1尾巴对于配体结合后的事件是必需的,例如细胞铺展以及肌动蛋白应力纤维的形成。在本文中,我们报道缺乏α1整合素亚基胞质结构域的细胞无法形成合适的粘着斑,并且在α1β1特异性底物上粘着斑成分酪氨酸残基的磷酸化减少。α1胞质序列是诸如桩蛋白、踝蛋白、α辅肌动蛋白和pp125FAK等粘着斑成分的特异性识别位点。它似乎解释了α1特异性信号传导,因为当模拟α1胞质结构域的肽转入细胞时,它们会影响α1β1特异性黏附,大概是通过竞争结合伴侣来实现的。对于α1整合素/蛋白结合,保守的赖氨酸-异亮氨酸-甘氨酸-苯丙氨酸-苯丙氨酸-赖氨酸-精氨酸基序,尤其是两个赖氨酸残基,是重要的。