Peus D, Meves A, Vasa R A, Beyerle A, O'Brien T, Pittelkow M R
Department of Dermatology, Mayo Clinic/Foundation, Rochester, MN, USA.
Free Radic Biol Med. 1999 Dec;27(11-12):1197-202. doi: 10.1016/s0891-5849(99)00198-7.
Ultraviolet radiation (UVR)-induced receptor phosphorylation is increasingly recognized as a widely occurring phenomenon. However, the mechanisms, mediators, and sequence of events involved in this process remain ill-defined. We have recently shown that exposure of human keratinocytes to physiologic doses of ultraviolet B radiation (UVB) activates epidermal growth factor receptor (EGFR)/extracellular-regulated kinase 1 and 2 (ERK1/2), and p38 signaling pathways via reactive oxygen species. Here we demonstrate that UVB exposure increased intra- and extracellular H2O2 production rapidly in a time-dependent manner. An EGFR-specific monoclonal antibody abrogated EGFR autophosphorylation and markedly decreased the phosphorylation of ERK1/2 whereas p38 activation was unaffected. Overexpression of catalase strongly inhibited UVB-induced EGFR/ERK1/2 pathway activation. These findings establish the sequence of events after UVB irradiation: (i) H2O2 generation, (ii) EGFR phosphorylation, and (iii) ERK activation. Our results identify UVB-induced H2O2 as a second messenger that is required for EGFR and dependent downstream signaling pathways activation.
紫外线辐射(UVR)诱导的受体磷酸化日益被认为是一种广泛存在的现象。然而,该过程中涉及的机制、介质和事件顺序仍不明确。我们最近发现,将人角质形成细胞暴露于生理剂量的紫外线B辐射(UVB)会通过活性氧激活表皮生长因子受体(EGFR)/细胞外调节激酶1和2(ERK1/2)以及p38信号通路。在此我们证明,UVB照射能迅速以时间依赖性方式增加细胞内和细胞外H2O2的产生。一种EGFR特异性单克隆抗体消除了EGFR自身磷酸化,并显著降低了ERK1/2的磷酸化,而p38的激活不受影响。过氧化氢酶的过表达强烈抑制了UVB诱导的EGFR/ERK1/2通路激活。这些发现确定了UVB照射后的事件顺序:(i)H2O2生成,(ii)EGFR磷酸化,以及(iii)ERK激活。我们的结果确定UVB诱导的H2O2作为一种第二信使,是EGFR及相关下游信号通路激活所必需的。