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Two distinct mechanisms by which phospholipase C-γ1 mediates epidermal growth factor-induced keratinocyte migration and proliferation

机译:磷脂酶C-γ1介导表皮生长因子诱导的角质形成细胞迁移和增殖的两种不同机制

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摘要

Keratinocyte migration and proliferation are essential steps for re-epithelialization in wound repair, and stimulated by the members of epidermal growth factor (EGF) family [1,2]. The receptor for these ligands is the epidermal growth factor receptor (EGFR). Activation of EGFR leads to receptor tyrosine kinase activation and a series of downstream signaling pathways, one of which is mediated by phospholipase C-gammaI (PLC-gammaI) [3]. PLC-gammaI is ubiquitously expressed in human tissues and contains two Src homology 2 (SH_2), one Src homology 3 (SH_3), one pleckstrin homology (PH), and two catalytic domains.
机译:角质形成细胞的迁移和增殖是伤口修复中重新上皮形成的必要步骤,并受到表皮生长因子(EGF)家族成员的刺激[1,2]。这些配体的受体是表皮生长因子受体(EGFR)。 EGFR的激活导致受体酪氨酸激酶的激活和一系列下游信号通路,其中之一由磷脂酶C-γI(PLC-gammaI)介导[3]。 PLC-γI在人的组织中普遍表达,并包含两个Src同源物2(SH_2),一个Src同源物3(SH_3),一个pleckstrin同源物(PH)和两个催化域。

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