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首页> 外文期刊>Biochemical and Biophysical Research Communications >Tissue kallikrein induces SH-SY5Y cell proliferation via epidermal growth factor receptor and extracellular signal-regulated kinase1/2 pathway
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Tissue kallikrein induces SH-SY5Y cell proliferation via epidermal growth factor receptor and extracellular signal-regulated kinase1/2 pathway

机译:组织激肽释放酶通过表皮生长因子受体和细胞外信号调节激酶1/2途径诱导SH-SY5Y细胞增殖

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摘要

Tissue kallikrein (TK) is well known to take most of its biological functions through bradykinin receptors. In the present study, we found a novel signaling pathway mediated by TK through epidermal growth factor receptor (EGFR) in human SH-SY5Y cells. We discovered that TK facilitated the activation of EGFR, extracellular signal-regulated kinase (ERK) 1/2 and p38 cascade. Interestingly, not p38 but ERK1/2 phosphorylation was severely compromised in cells depleted of EGFR. Nevertheless, impairment of signaling of ERK1/2 seemed not to be restricted to EGFR phosphorylation. We also observed that TK stimulation could induce SH-SY5Y cell proliferation, which was reduced by EGFR down-regulation or ERK1/2 inhibitor. Overall, our findings provided convincing evidence that TK could mediate cell proliferation via EGFR and ERK1/2 pathway in vitro.
机译:组织激肽释放酶(TK)通过缓激肽受体发挥其大部分生物学功能。在本研究中,我们发现人SH-SY5Y细胞中由TK通过表皮生长因子受体(EGFR)介导的新型信号通路。我们发现TK促进了EGFR,细胞外信号调节激酶(ERK)1/2和p38级联的激活。有趣的是,在缺乏EGFR的细胞中,不是p38而是ERK1 / 2磷酸化严重受损。然而,ERK1 / 2信号转导的损伤似乎并不限于EGFR磷酸化。我们还观察到,TK刺激可以诱导SH-SY5Y细胞增殖,这被EGFR下调或ERK1 / 2抑制剂抑制。总体而言,我们的发现提供了令人信服的证据,表明TK可以在体外通过EGFR和ERK1 / 2途径介导细胞增殖。

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