Ray Ramesh M, Bhattacharya Sujoy, Johnson Leonard R
Department of Physiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Cell Signal. 2007 Dec;19(12):2519-27. doi: 10.1016/j.cellsig.2007.08.001. Epub 2007 Aug 15.
Intracellular polyamine synthesis is regulated by the enzyme ornithine decarboxylase (ODC), and its inhibition by alpha-difluromethylornithine (DFMO), confers resistance to apoptosis. We have previously shown that DFMO leads to the inhibition of de novo polyamine synthesis, which in turn rapidly activates Src, STAT3 and NF-kappaB via integrin beta3 in intestinal epithelial cells. One mechanism to explain these effects involves the activation of upstream growth factor receptors, such as the epidermal growth factor receptor (EGFR). We therefore hypothesized that EGFR phosphorylation regulates the early response to polyamine depletion. DFMO increased EGFR phosphorylation on tyrosine residues 1173 (pY1173) and 845 (pY845) within 5 min. Phosphorylation declined after 10 min and was prevented by the addition of exogenous putrescine to DFMO containing medium. Phosphorylation of EGFR was concomitant with the activation of ERK1/2. Pretreatment with either DFMO or EGF for 1 h protected cells from TNF-alpha/CHX-induced apoptosis. Exogenous addition of polyamines prevented the protective effect of DFMO. In addition, inhibition of integrin beta3 activity (with RGDS), Src activity (with PP2), or EGFR kinase activity (with AG1478), increased basal apoptosis and prevented protection conferred by either DFMO or EGF. Polyamine depletion failed to protect B82L fibroblasts lacking the EGFR (PRN) and PRN cells expressing either a kinase dead EGFR (K721A) or an EGFR (Y845F) mutant lacking the Src phosphorylation site. Conversely, expression of WT-EGFR (WT) restored the protective effect of polyamine depletion. Fibronectin activated the EGFR, Src, ERKs and protected cells from apoptosis. Taken together, our data indicate an essential role of EGFR kinase activity in MEK/ERK-mediated protection, which synergizes with integrin beta3 leading to Src-mediated protective responses in polyamine depleted cells.
细胞内多胺合成受鸟氨酸脱羧酶(ODC)调控,α-二氟甲基鸟氨酸(DFMO)对其的抑制作用赋予细胞对凋亡的抗性。我们之前已表明,DFMO导致从头合成多胺受到抑制,进而通过肠上皮细胞中的整合素β3迅速激活Src、STAT3和NF-κB。解释这些效应的一种机制涉及上游生长因子受体的激活,如表皮生长因子受体(EGFR)。因此,我们推测EGFR磷酸化调节对多胺耗竭的早期反应。DFMO在5分钟内增加了酪氨酸残基1173(pY1173)和845(pY845)处的EGFR磷酸化。10分钟后磷酸化水平下降,向含DFMO的培养基中添加外源性腐胺可阻止这种下降。EGFR的磷酸化与ERK1/2的激活同时发生。用DFMO或EGF预处理1小时可保护细胞免受TNF-α/CHX诱导的凋亡。外源性添加多胺可消除DFMO的保护作用。此外,抑制整合素β3活性(用RGDS)、Src活性(用PP2)或EGFR激酶活性(用AG1478),会增加基础凋亡并阻止DFMO或EGF赋予的保护作用。多胺耗竭无法保护缺乏EGFR的B82L成纤维细胞(PRN)以及表达激酶失活的EGFR(K721A)或缺乏Src磷酸化位点的EGFR(Y845F)突变体的PRN细胞。相反,野生型EGFR(WT)的表达恢复了多胺耗竭的保护作用。纤连蛋白激活EGFR、Src、ERK并保护细胞免受凋亡。综上所述,我们的数据表明EGFR激酶活性在MEK/ERK介导的保护中起关键作用,它与整合素β3协同作用,在多胺耗竭的细胞中引发Src介导的保护反应。