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Epidermal growth factor induction of front–rear polarity and migration in keratinocytes is mediated by integrin-linked kinase and ELMO2

机译:表皮生长因子诱导角质形成细胞的前后极性和迁移是由整合素连接的激酶和ELMO2介导的

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摘要

Epidermal growth factor (EGF) is a potent chemotactic and mitogenic factor for epidermal keratinocytes, and these properties are central for normal epidermal regeneration after injury. The involvement of mitogen-activated protein kinases as mediators of the proliferative effects of EGF is well established. However, the molecular mechanisms that mediate motogenic responses to this growth factor are not clearly understood. An obligatory step for forward cell migration is the development of front–rear polarity and formation of lamellipodia at the leading edge. We show that stimulation of epidermal keratinocytes with EGF, but not with other growth factors, induces development of front–rear polarity and directional migration through a pathway that requires integrin-linked kinase (ILK), Engulfment and Cell Motility-2 (ELMO2), integrin β1, and Rac1. Furthermore, EGF induction of front–rear polarity and chemotaxis require the tyrosine kinase activity of the EGF receptor and are mediated by complexes containing active RhoG, ELMO2, and ILK. Our findings reveal a novel link between EGF receptor stimulation, ILK-containing complexes, and activation of small Rho GTPases necessary for acquisition of front–rear polarity and forward movement.
机译:表皮生长因子(EGF)是表皮角质形成细胞的一种强大的趋化因子和促有丝分裂因子,这些特性对于损伤后正常的表皮再生至关重要。丝裂原活化的蛋白激酶作为EGF的增殖作用的介体的参与已得到充分证实。然而,尚不清楚介导对此生长因子的致机能性反应的分子机制。细胞向前迁移的必不可少的步骤是前后极性的发展以及在前缘形成片状脂膜。我们发现,用EGF刺激表皮角质形成细胞,而不是用其他生长因子刺激,会通过需要整合素连接激酶(ILK),吞噬和细胞运动2(ELMO2)的途径诱导前后极性和定向迁移的发展,整合素β1和Rac1。此外,EGF诱导前后极性和趋化性需要EGF受体的酪氨酸激酶活性,并由含有活性RhoG,ELMO2和ILK的复合物介导。我们的发现揭示了EGF受体刺激,含ILK的复合物与激活前后极性和向前运动所需的小Rho GTPases活化之间的新型联系。

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