Developmental Genetics Laboratory, London Research Institute, Cancer Research UK, 44 Lincoln's Inn Fields, London WC2A 4LY, UK.
Development. 2010 Nov;137(21):3591-601. doi: 10.1242/dev.050070. Epub 2010 Sep 28.
Integrins act at signalling crossroads, and their interactions with other signal transduction pathways are key to the regulation of normal and pathological cell cytoarchitecture and behaviour. Here, we describe a signalling cascade that acts during the formation of the defining segmental features of the vertebrate body - the somites - in which β1-integrin activity regulates epithelialisation by controlling downstream Wnt and Notch activity crucial for somite border formation. Using in vivo transcriptional inhibition in the developing chick embryo, we show that β1-integrin in the anterior presomitic mesoderm activates canonical Wnt signalling in a cell-autonomous, `outside-inside' manner. Signalling is mediated by integrin-linked kinase (ILK), leading to modulation of glycogen synthase kinase 3β (GSK3β) phosphorylation, and activates Notch signalling in the anterior presomitic mesoderm. The two signalling pathways then cooperate to promote somite formation via cMESO1/Mesp2. Our results show that β1-integrin can regulate cell shape and tissue morphogenesis indirectly, by regulation of downstream signalling cascades.
整合素在信号交汇点发挥作用,它们与其他信号转导途径的相互作用是调节正常和病理细胞细胞形态和行为的关键。在这里,我们描述了一个信号级联反应,它在形成脊椎动物身体的定义节段特征(体节)的过程中发挥作用,β1-整合素通过控制对体节边界形成至关重要的下游 Wnt 和 Notch 活性来调节上皮化。我们使用在发育中的鸡胚中的体内转录抑制,表明前体节中胚层中的β1-整合素以细胞自主的“外向内”方式激活经典 Wnt 信号。信号由整合素连接激酶 (ILK) 介导,导致糖原合酶激酶 3β (GSK3β) 磷酸化的调节,并在前体节中胚层中激活 Notch 信号。然后,这两个信号通路通过促进 cMESO1/Mesp2 的形成来共同促进体节形成。我们的结果表明,β1-整合素可以通过调节下游信号级联反应间接调节细胞形状和组织形态发生。