色素上皮衍生因子通过激活培养的视网膜色素上皮细胞中的细胞外信号调节激酶来抑制氧化应激诱导的细胞死亡。

Pigment epithelium-derived factor inhibits oxidative stress-induced cell death by activation of extracellular signal-regulated kinases in cultured retinal pigment epithelial cells.

作者信息

Tsao Yeou-Ping, Ho Tsung-Chuan, Chen Show-Li, Cheng Huey-Chuan

机构信息

Department of Ophthalmology, Mackay Memorial Hospital, Taipei, Taiwan.

出版信息

Life Sci. 2006 Jul 4;79(6):545-50. doi: 10.1016/j.lfs.2006.01.041. Epub 2006 Feb 28.

Abstract

Oxidative stress-induced retinal pigment epithelial (RPE) cell death is involved in the pathogenesis of age-related macular degeneration (AMD). Pigment epithelium-derived factor (PEDF) is an anti-angiogenic/neurotropic dual functional factor, and recently it was also shown to mediate anti-oxidative action. In the present study, the influence of PEDF in hydrogen peroxide (H(2)O(2))-induced RPE cell death was investigated using nontransformed human RPE cell line (ARPE-19). The recombinant PEDF was purified from E. coli. The MTT cell viability assay showed that PEDF rescued ARPE-19 from H(2)O(2)-induced cell death in a dose- and time-dependent manner. Western blot analysis revealed that PEDF stimulated the extracellular signal-regulated kinases (ERK1/2) phosphorylation. The PEDF cytoprotective effect was significantly attenuated by the ERK1/2 inhibitor PD98059. In this study, we demonstrate that PEDF induces ERK1/2 phosphorylation and we further suggest that the ERK signal cascade contributes to RPE cell's cytoprotection against oxidative stress.

摘要

氧化应激诱导的视网膜色素上皮(RPE)细胞死亡参与年龄相关性黄斑变性(AMD)的发病机制。色素上皮衍生因子(PEDF)是一种具有抗血管生成/神经营养双重功能的因子,最近还显示其具有抗氧化作用。在本研究中,使用未转化的人RPE细胞系(ARPE-19)研究了PEDF对过氧化氢(H₂O₂)诱导的RPE细胞死亡的影响。重组PEDF从大肠杆菌中纯化得到。MTT细胞活力测定表明,PEDF以剂量和时间依赖性方式挽救ARPE-19细胞免受H₂O₂诱导的细胞死亡。蛋白质印迹分析显示,PEDF刺激细胞外信号调节激酶(ERK1/2)磷酸化。ERK1/2抑制剂PD98059可显著减弱PEDF的细胞保护作用。在本研究中,我们证明PEDF诱导ERK1/2磷酸化,并进一步表明ERK信号级联有助于RPE细胞抵抗氧化应激的细胞保护作用。

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