He Shikun, Yaung Jennifer, Kim Yeong Hoon, Barron Ernesto, Ryan Stephen J, Hinton David R
Department of Pathology, Keck School of Medicine of the University of Southern California, 2011 Zonal Ave., HMR 209, Los Angeles, CA 90033, USA.
Graefes Arch Clin Exp Ophthalmol. 2008 May;246(5):677-83. doi: 10.1007/s00417-008-0770-2. Epub 2008 Feb 16.
Induction of glucose-regulated protein (GRP)-78 in the endoplasmic reticulum (ER) is a protective mechanism cells use to adapt to ER stress. We evaluated the expression of GRP-78 and its regulation by an oxidant tert-butyl hydroperoxide (tBH) in human retinal pigment epithelium (RPE) cells.
We used a carboxy-H2-DCFDA staining method to detect tBH-induced accumulation of reactive oxygen species (ROS) in RPE cells, and analyzed the expression of GRP-78 in normal human fetal and adult retinas and in cultured human RPE cells by immunohistochemistry. The effects of tBH (10-100 microM) on GRP-78 and on growth arrest and DNA damage inducible genes 153 (GADD153) protein and mRNA expression were studied using Western blot and real-time polymerase chain reaction.
Sections of fetal retinas were negative for GRP-78. Adult retinas showed moderate cytoplasmic GRP-78 staining in the RPE and choroid. tBH-induced ROS accumulation in RPE cells showed partial colocalization with the ER. GRP-78 and GADD153 mRNA and protein expression in cultured RPE cells were significantly upregulated by treatment with tBH.
tBH increases oxidative stress, increases accumulation of ROS in the ER, and upregulates expression of GRP-78 and GADD153. This supports the connection between oxidative stress and ER stress, and suggests that GRP-78 may serve a protective role in the RPE response to oxidative stress.
内质网(ER)中葡萄糖调节蛋白(GRP)-78的诱导是细胞用于适应内质网应激的一种保护机制。我们评估了GRP-78在人视网膜色素上皮(RPE)细胞中的表达及其受氧化剂叔丁基过氧化氢(tBH)的调节。
我们使用羧基-H2-DCFDA染色法检测tBH诱导的RPE细胞中活性氧(ROS)的积累,并通过免疫组织化学分析GRP-78在正常人类胎儿和成人视网膜以及培养的人RPE细胞中的表达。使用蛋白质印迹法和实时聚合酶链反应研究了tBH(10-100 microM)对GRP-78以及生长停滞和DNA损伤诱导基因153(GADD153)蛋白和mRNA表达的影响。
胎儿视网膜切片GRP-78呈阴性。成人视网膜在RPE和脉络膜中显示出中等程度细胞质GRP-78染色。tBH诱导的RPE细胞中ROS积累与内质网部分共定位。tBH处理后,培养的RPE细胞中GRP-78和GADD153的mRNA及蛋白表达显著上调。
tBH增加氧化应激,增加内质网中ROS的积累,并上调GRP-78和GADD153的表达。这支持了氧化应激与内质网应激之间的联系,并表明GRP-78可能在RPE对氧化应激的反应中起保护作用。