Skip to main content
Erschienen in: Graefe's Archive for Clinical and Experimental Ophthalmology 5/2008

01.05.2008 | Basic Science

Endoplasmic reticulum stress induced by oxidative stress in retinal pigment epithelial cells

verfasst von: Shikun He, Jennifer Yaung, Yeong Hoon Kim, Ernesto Barron, Stephen J. Ryan, David R. Hinton

Erschienen in: Graefe's Archive for Clinical and Experimental Ophthalmology | Ausgabe 5/2008

Einloggen, um Zugang zu erhalten

Abstract

Background

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.

Methods

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 μM) 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.

Results

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.

Conclusion

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.
Literatur
1.
Zurück zum Zitat Barnes JA, Smoak IW (2000) Glucose-regulated protein 78 (GRP78) is elevated in embryonic mouse heart and induced following hypoglycemic stress. Anat Embryol (Berl) 202:67–74CrossRef Barnes JA, Smoak IW (2000) Glucose-regulated protein 78 (GRP78) is elevated in embryonic mouse heart and induced following hypoglycemic stress. Anat Embryol (Berl) 202:67–74CrossRef
2.
Zurück zum Zitat Brewster JL, Linseman DA, Bouchard RJ, Loucks FA, Precht TA, Esch EA, Heidenreich KA (2006) Endoplasmic reticulum stress and trophic factor withdrawal activate distinct signaling cascades that induce glycogen synthase kinase-3 beta and a caspase-9-dependent apoptosis in cerebellar granule neurons. Mol Cell Neurosci 32:242–253PubMedCrossRef Brewster JL, Linseman DA, Bouchard RJ, Loucks FA, Precht TA, Esch EA, Heidenreich KA (2006) Endoplasmic reticulum stress and trophic factor withdrawal activate distinct signaling cascades that induce glycogen synthase kinase-3 beta and a caspase-9-dependent apoptosis in cerebellar granule neurons. Mol Cell Neurosci 32:242–253PubMedCrossRef
3.
Zurück zum Zitat Chen L, Gao X (2002) Neuronal apoptosis induced by endoplasmic reticulum stress. Neurochem Res 27:891–898PubMedCrossRef Chen L, Gao X (2002) Neuronal apoptosis induced by endoplasmic reticulum stress. Neurochem Res 27:891–898PubMedCrossRef
4.
Zurück zum Zitat Dey A, Kessova IG, Cederbaum AI (2006) Decreased protein and mRNA expression of ER stress proteins GRP-78 and GRP94 in HepG2 cells over-expressing CYP2E1. Arch Biochem Biophys 447:155–166PubMedCrossRef Dey A, Kessova IG, Cederbaum AI (2006) Decreased protein and mRNA expression of ER stress proteins GRP-78 and GRP94 in HepG2 cells over-expressing CYP2E1. Arch Biochem Biophys 447:155–166PubMedCrossRef
5.
Zurück zum Zitat Forman MS, Lee VM, Trojanowski JQ (2003) “Unfolding” pathways in neurodegenerative disease. Trends Neurosci 26:407–410PubMedCrossRef Forman MS, Lee VM, Trojanowski JQ (2003) “Unfolding” pathways in neurodegenerative disease. Trends Neurosci 26:407–410PubMedCrossRef
6.
Zurück zum Zitat Ghribi O (2006) The role of the endoplasmic reticulum in the accumulation of beta-amyloid peptide in Alzheimer’s disease. Curr Mol Med 6:119–133PubMedCrossRef Ghribi O (2006) The role of the endoplasmic reticulum in the accumulation of beta-amyloid peptide in Alzheimer’s disease. Curr Mol Med 6:119–133PubMedCrossRef
7.
Zurück zum Zitat Ghribi O, Herman MM, DeWitt DA, Forbes MS, Savory J (2001) Abeta(1–42) and aluminum induce stress in the endoplasmic reticulum in rabbit hippocampus, involving nuclear translocation of GADD153 and NF-kappaB. Brain Res Mol Brain Res 96:30–38PubMedCrossRef Ghribi O, Herman MM, DeWitt DA, Forbes MS, Savory J (2001) Abeta(1–42) and aluminum induce stress in the endoplasmic reticulum in rabbit hippocampus, involving nuclear translocation of GADD153 and NF-kappaB. Brain Res Mol Brain Res 96:30–38PubMedCrossRef
8.
Zurück zum Zitat Ghribi O, Herman MM, Pramoonjago P, Spaulding NK, Savory J (2004) GDNF regulates the A beta-induced endoplasmic reticulum stress response in rabbit hippocampus by inhibiting the activation of GADD153 and the JNK and ERK kinases. Neurobiol Dis 16:417–427PubMedCrossRef Ghribi O, Herman MM, Pramoonjago P, Spaulding NK, Savory J (2004) GDNF regulates the A beta-induced endoplasmic reticulum stress response in rabbit hippocampus by inhibiting the activation of GADD153 and the JNK and ERK kinases. Neurobiol Dis 16:417–427PubMedCrossRef
9.
Zurück zum Zitat Gomer CJ, Ferrario A, Rucker N, Wong S, Lee AS (1991) Glucose regulated protein induction and cellular resistance to oxidative stress mediated by porphyrin photosensitization. Cancer Res 51:6574–6579PubMed Gomer CJ, Ferrario A, Rucker N, Wong S, Lee AS (1991) Glucose regulated protein induction and cellular resistance to oxidative stress mediated by porphyrin photosensitization. Cancer Res 51:6574–6579PubMed
10.
Zurück zum Zitat Guo ZH, Mattson MP (2000) In vivo 2-deoxyglucose administration preserves glucose and glutamate transport and mitochondrial function in cortical synaptic terminals after exposure to amyloid beta-peptide and iron: evidence for a stress response. Exp Neurol 166:173–179PubMedCrossRef Guo ZH, Mattson MP (2000) In vivo 2-deoxyglucose administration preserves glucose and glutamate transport and mitochondrial function in cortical synaptic terminals after exposure to amyloid beta-peptide and iron: evidence for a stress response. Exp Neurol 166:173–179PubMedCrossRef
11.
Zurück zum Zitat Guyton KZ, Xu Q, Holbrook NJ (1996) Induction of the mammalian stess response gene GADD153 by oxidative stress:role of AP-1 element. Biochem J 314:547–554PubMed Guyton KZ, Xu Q, Holbrook NJ (1996) Induction of the mammalian stess response gene GADD153 by oxidative stress:role of AP-1 element. Biochem J 314:547–554PubMed
12.
Zurück zum Zitat Ha KN, Chen Y, Cai J, Sternberg P Jr (2006) Increased glutathione synthesis through an ARE-Nrf2-dependent pathway by zinc in the RPE: implication for protection against oxidative stress. Invest Ophthalmol Vis Sci 47:2709–2715PubMedCrossRef Ha KN, Chen Y, Cai J, Sternberg P Jr (2006) Increased glutathione synthesis through an ARE-Nrf2-dependent pathway by zinc in the RPE: implication for protection against oxidative stress. Invest Ophthalmol Vis Sci 47:2709–2715PubMedCrossRef
13.
Zurück zum Zitat Hashimoto M, Rockenstein E, Crews L, Masliah E (2003) Role of protein aggregation in mitochondrial dysfunction and neurodegeneration in Alzheimer’s and Parkinson’s diseases. Neuromolecular Med 4:21–36PubMedCrossRef Hashimoto M, Rockenstein E, Crews L, Masliah E (2003) Role of protein aggregation in mitochondrial dysfunction and neurodegeneration in Alzheimer’s and Parkinson’s diseases. Neuromolecular Med 4:21–36PubMedCrossRef
14.
Zurück zum Zitat Hayashi T, Saito A, Okuno S, Ferrand-Drake M, Dodd RL, Chan PH (2005) Damage to the endoplasmic reticulum and activation of apoptotic machinery by oxidative stress in ischemic neurons. J Cereb Blood Flow Metab 25:41–53PubMedCrossRef Hayashi T, Saito A, Okuno S, Ferrand-Drake M, Dodd RL, Chan PH (2005) Damage to the endoplasmic reticulum and activation of apoptotic machinery by oxidative stress in ischemic neurons. J Cereb Blood Flow Metab 25:41–53PubMedCrossRef
15.
Zurück zum Zitat Imaizumi K, Miyoshi K, Katayama T, Yoneda T, Taniguchi M, Kudo T, Tohyama M (2001) The unfolded protein response and Alzheimer’s disease. Biochim Biophys Acta 1536:85–96PubMed Imaizumi K, Miyoshi K, Katayama T, Yoneda T, Taniguchi M, Kudo T, Tohyama M (2001) The unfolded protein response and Alzheimer’s disease. Biochim Biophys Acta 1536:85–96PubMed
16.
Zurück zum Zitat Jin M, Yaung J, Kannan R, He S, Ryan SJ, Hinton DR (2005) Hepatocyte growth factor protects RPE cells from apoptosis induced by glutathione depletion. Invest Ophthalmol Vis Sci 46:4311–4319PubMedCrossRef Jin M, Yaung J, Kannan R, He S, Ryan SJ, Hinton DR (2005) Hepatocyte growth factor protects RPE cells from apoptosis induced by glutathione depletion. Invest Ophthalmol Vis Sci 46:4311–4319PubMedCrossRef
17.
Zurück zum Zitat Kannan R, Jin M, Gamulescu MA, Hinton DR (2004) Ceramide-induced apoptosis: role of catalase and hepatocyte growth factor. Free Radic Biol Med 37:166–175PubMedCrossRef Kannan R, Jin M, Gamulescu MA, Hinton DR (2004) Ceramide-induced apoptosis: role of catalase and hepatocyte growth factor. Free Radic Biol Med 37:166–175PubMedCrossRef
18.
Zurück zum Zitat Kasahara E, Lin LR, Ho YS, Reddy VN (2005) SOD2 protects against oxidation-induced apoptosis in mouse retinal pigment epithelium: implications for age-related macular degeneration. Invest Ophthalmol Vis Sci 46:3426–3434PubMedCrossRef Kasahara E, Lin LR, Ho YS, Reddy VN (2005) SOD2 protects against oxidation-induced apoptosis in mouse retinal pigment epithelium: implications for age-related macular degeneration. Invest Ophthalmol Vis Sci 46:3426–3434PubMedCrossRef
19.
Zurück zum Zitat Katayama T, Imaizumi K, Manabe T, Hitomi J, Kudo T, Tohyama M (2004) Induction of neuronal death by ER stress in Alzheimer’s disease. J Chem Neuroanat 28:67–78PubMedCrossRef Katayama T, Imaizumi K, Manabe T, Hitomi J, Kudo T, Tohyama M (2004) Induction of neuronal death by ER stress in Alzheimer’s disease. J Chem Neuroanat 28:67–78PubMedCrossRef
20.
Zurück zum Zitat King A, Gottlieb E, Brooks DG, Murphy MP, Dunaief JL (2004) Mitochondria-derived reactive oxygen species mediate blue light-induced death of retinal pigment epithelial cells. Photochem Photobiol 79:470–475PubMedCrossRef King A, Gottlieb E, Brooks DG, Murphy MP, Dunaief JL (2004) Mitochondria-derived reactive oxygen species mediate blue light-induced death of retinal pigment epithelial cells. Photochem Photobiol 79:470–475PubMedCrossRef
21.
Zurück zum Zitat Kline CL, Schrufer TL, Jefferson LS, Kimball SR (2006) Glucosamine-induced phosphorylation of the alpha-subunit of eukaryotic initiation factor 2 is mediated by the protein kinase R-like endoplasmic-reticulum associated kinase. Int J Biochem Cell Biol 38:1004–1014PubMedCrossRef Kline CL, Schrufer TL, Jefferson LS, Kimball SR (2006) Glucosamine-induced phosphorylation of the alpha-subunit of eukaryotic initiation factor 2 is mediated by the protein kinase R-like endoplasmic-reticulum associated kinase. Int J Biochem Cell Biol 38:1004–1014PubMedCrossRef
22.
Zurück zum Zitat Kudo T, Okumura M, Imaizumi K, Araki W, Morihara T, Tanimukai H, Kamagata E, Tabuchi N, Kimura R, Kanayama D, Fukumori A, Tagami S, Okochi M, Kubo M, Tanii H, Tohyama M, Tabira T, Takeda M (2006) Altered localization of amyloid precursor protein under endoplasmic reticulum stress. Biochem Biophys Res Commun 344:525–530PubMedCrossRef Kudo T, Okumura M, Imaizumi K, Araki W, Morihara T, Tanimukai H, Kamagata E, Tabuchi N, Kimura R, Kanayama D, Fukumori A, Tagami S, Okochi M, Kubo M, Tanii H, Tohyama M, Tabira T, Takeda M (2006) Altered localization of amyloid precursor protein under endoplasmic reticulum stress. Biochem Biophys Res Commun 344:525–530PubMedCrossRef
23.
Zurück zum Zitat Kuznetsov G, Bush KT, Zhang PL, Nigam SK (1996) Perturbations in maturation of secretory proteins and their association with endoplasmic reticulum chaperones in a cell culture model for epithelial ischemia. Proc Natl Acad Sci USA 93:8584–8589PubMedCrossRef Kuznetsov G, Bush KT, Zhang PL, Nigam SK (1996) Perturbations in maturation of secretory proteins and their association with endoplasmic reticulum chaperones in a cell culture model for epithelial ischemia. Proc Natl Acad Sci USA 93:8584–8589PubMedCrossRef
24.
Zurück zum Zitat Lai MT, Huang KL, Chang WM, Lai YK (2003) Geldanamycin induction of GRP-78 requires activation of reactive oxygen species via ER stress responsive elements in 9 L rat brain tumour cells. Cell Signal 15:585–595PubMedCrossRef Lai MT, Huang KL, Chang WM, Lai YK (2003) Geldanamycin induction of GRP-78 requires activation of reactive oxygen species via ER stress responsive elements in 9 L rat brain tumour cells. Cell Signal 15:585–595PubMedCrossRef
25.
Zurück zum Zitat Le Bras M, Rouy I, Brenner C (2006) The modulation of inter-organelle cross-talk to control apoptosis. Med Chem 2:1–12PubMedCrossRef Le Bras M, Rouy I, Brenner C (2006) The modulation of inter-organelle cross-talk to control apoptosis. Med Chem 2:1–12PubMedCrossRef
26.
Zurück zum Zitat Gilmore WJ, Kirby GM (2004) Endoplasmic reticulum stress due to altered cellular redox status positively regulates murine hepatic CYP2A5 expression. J Pharmacol Exp Ther 308:600–608PubMedCrossRef Gilmore WJ, Kirby GM (2004) Endoplasmic reticulum stress due to altered cellular redox status positively regulates murine hepatic CYP2A5 expression. J Pharmacol Exp Ther 308:600–608PubMedCrossRef
27.
Zurück zum Zitat Lee AS (1992) Mammalian stress response: induction of the glucose-regulated protein family. Curr Opin Cell Biol 4:267–273PubMedCrossRef Lee AS (1992) Mammalian stress response: induction of the glucose-regulated protein family. Curr Opin Cell Biol 4:267–273PubMedCrossRef
28.
Zurück zum Zitat Lee AS (2001) The glucose-regulated proteins: stress induction and clinical applications. Trends Biochem Sci 26:504–510PubMedCrossRef Lee AS (2001) The glucose-regulated proteins: stress induction and clinical applications. Trends Biochem Sci 26:504–510PubMedCrossRef
29.
Zurück zum Zitat Li B, Chen YH (2003) [The expression of glucose-regulated protein 78 (GRP78) in mouse brain during early development]. Shi Yan Sheng Wu Xue Bao 36:137–144PubMed Li B, Chen YH (2003) [The expression of glucose-regulated protein 78 (GRP78) in mouse brain during early development]. Shi Yan Sheng Wu Xue Bao 36:137–144PubMed
30.
Zurück zum Zitat Liang FQ, Godley BF (2003) Oxidative stress-induced mitochondrial DNA damage in human retinal pigment epithelial cells: a possible mechanism for RPE aging and age-related macular degeneration. Exp Eye Res 76:397–403PubMedCrossRef Liang FQ, Godley BF (2003) Oxidative stress-induced mitochondrial DNA damage in human retinal pigment epithelial cells: a possible mechanism for RPE aging and age-related macular degeneration. Exp Eye Res 76:397–403PubMedCrossRef
31.
Zurück zum Zitat Liang FQ, Green L, Wang C, Alssadi R, Godley BF (2004) Melatonin protects human retinal pigment epithelial (RPE) cells against oxidative stress. Exp Eye Res 78:1069–1075PubMedCrossRef Liang FQ, Green L, Wang C, Alssadi R, Godley BF (2004) Melatonin protects human retinal pigment epithelial (RPE) cells against oxidative stress. Exp Eye Res 78:1069–1075PubMedCrossRef
32.
Zurück zum Zitat Lindholm D, Wootz H, Korhonen L (2006) ER stress and neurodegenerative diseases. Cell Death Differ 13:385–392PubMedCrossRef Lindholm D, Wootz H, Korhonen L (2006) ER stress and neurodegenerative diseases. Cell Death Differ 13:385–392PubMedCrossRef
33.
Zurück zum Zitat Lu L, Hackett SF, Mincey A, Lai H, Campochiaro PA (2006) Effects of different types of oxidative stress in RPE cells. J Cell Physiol 206:119–125PubMedCrossRef Lu L, Hackett SF, Mincey A, Lai H, Campochiaro PA (2006) Effects of different types of oxidative stress in RPE cells. J Cell Physiol 206:119–125PubMedCrossRef
34.
Zurück zum Zitat Mattson MP (2006) Neuronal life-and-death signaling, apoptosis, and neurodegenerative disorders. Antioxid Redox Signal 8:1997–2006PubMedCrossRef Mattson MP (2006) Neuronal life-and-death signaling, apoptosis, and neurodegenerative disorders. Antioxid Redox Signal 8:1997–2006PubMedCrossRef
35.
Zurück zum Zitat Miceli MV, Liles MR, Newsome DA (1994) Evaluation of oxidative processes in human pigment epithelial cells associated with retinal outer segment phagocytosis. Exp Cell Res 214:242–249PubMedCrossRef Miceli MV, Liles MR, Newsome DA (1994) Evaluation of oxidative processes in human pigment epithelial cells associated with retinal outer segment phagocytosis. Exp Cell Res 214:242–249PubMedCrossRef
36.
Zurück zum Zitat Onoue S, Kumon Y, Igase K, Ohnishi T, Sakanaka M (2005) Growth arrest and DNA damage-inducible gene 153 increases transiently in the thalamus following focal cerebral infarction. Brain Res Mol Brain Res 134:189–197PubMedCrossRef Onoue S, Kumon Y, Igase K, Ohnishi T, Sakanaka M (2005) Growth arrest and DNA damage-inducible gene 153 increases transiently in the thalamus following focal cerebral infarction. Brain Res Mol Brain Res 134:189–197PubMedCrossRef
37.
Zurück zum Zitat Paschen W, Mengesdorf T, Althausen S, Hotop S (2001) Peroxidative stress selectively down-regulates the neuronal stress response activated under conditions of endoplasmic reticulum dysfunction. J Neurochem 76:1916–1924PubMedCrossRef Paschen W, Mengesdorf T, Althausen S, Hotop S (2001) Peroxidative stress selectively down-regulates the neuronal stress response activated under conditions of endoplasmic reticulum dysfunction. J Neurochem 76:1916–1924PubMedCrossRef
38.
Zurück zum Zitat Paz Gavilan M, Vela J, Castano A, Ramos B, del Rio JC, Vitorica J, Ruano D (2006) Cellular environment facilitates protein accumulation in aged rat hippocampus. Neurobiol Aging 27:973–982PubMedCrossRef Paz Gavilan M, Vela J, Castano A, Ramos B, del Rio JC, Vitorica J, Ruano D (2006) Cellular environment facilitates protein accumulation in aged rat hippocampus. Neurobiol Aging 27:973–982PubMedCrossRef
39.
Zurück zum Zitat Price BD, Mannheim-Rodman LA, Calderwood SK (1992) Brefeldin A, thapsigargin, and AIF4- stimulate the accumulation of GRP-78 mRNA in a cycloheximide dependent manner, whilst induction by hypoxia is independent of protein synthesis. J Cell Physiol 152:545–552PubMedCrossRef Price BD, Mannheim-Rodman LA, Calderwood SK (1992) Brefeldin A, thapsigargin, and AIF4- stimulate the accumulation of GRP-78 mRNA in a cycloheximide dependent manner, whilst induction by hypoxia is independent of protein synthesis. J Cell Physiol 152:545–552PubMedCrossRef
40.
Zurück zum Zitat Rao RV, Peel A, Logvinova A, del Rio G, Hermel E, Yokota T, Goldsmith PC, Ellerby LM, Ellerby HM, Bredesen DE (2002) Coupling endoplasmic reticulum stress to the cell death program: role of the ER chaperone GRP-78. FEBS Lett 514:122–128PubMed Rao RV, Peel A, Logvinova A, del Rio G, Hermel E, Yokota T, Goldsmith PC, Ellerby LM, Ellerby HM, Bredesen DE (2002) Coupling endoplasmic reticulum stress to the cell death program: role of the ER chaperone GRP-78. FEBS Lett 514:122–128PubMed
41.
Zurück zum Zitat Reddy RK, Mao C, Baumeister P, Austin RC, Kaufman RJ, Lee AS (2003) Endoplasmic reticulum chaperone protein GRP-78 protects cells from apoptosis induced by topoisomerase inhibitors: role of ATP binding site in suppression of caspase-7 activation. J Biol Chem 278:20915–20924PubMedCrossRef Reddy RK, Mao C, Baumeister P, Austin RC, Kaufman RJ, Lee AS (2003) Endoplasmic reticulum chaperone protein GRP-78 protects cells from apoptosis induced by topoisomerase inhibitors: role of ATP binding site in suppression of caspase-7 activation. J Biol Chem 278:20915–20924PubMedCrossRef
42.
Zurück zum Zitat Roth F, Bindewald A, Holz FG (2004) Keypathophysiologic pathways in age-related macular disease. Graefes Arch Clin Exp Ophthalmol 242:710–716PubMedCrossRef Roth F, Bindewald A, Holz FG (2004) Keypathophysiologic pathways in age-related macular disease. Graefes Arch Clin Exp Ophthalmol 242:710–716PubMedCrossRef
43.
Zurück zum Zitat Roybal CN, Marmorstein LY, Vander Jagt DL, Abcouwer SF (2005) Aberrant accumulation of fibulin-3 in the endoplasmic reticulum leads to activation of the unfolded protein response and VEGF expression. Invest Ophthalmol Vis Sci 46:3973–3979PubMedCrossRef Roybal CN, Marmorstein LY, Vander Jagt DL, Abcouwer SF (2005) Aberrant accumulation of fibulin-3 in the endoplasmic reticulum leads to activation of the unfolded protein response and VEGF expression. Invest Ophthalmol Vis Sci 46:3973–3979PubMedCrossRef
44.
Zurück zum Zitat Ryu EJ, Harding HP, Angelastro JM, Vitolo OV, Ron D, Greene LA (2002) Endoplasmic reticulum stress and the unfolded protein response in cellular models of Parkinson’s disease. J Neurosci 22:10690–10698PubMed Ryu EJ, Harding HP, Angelastro JM, Vitolo OV, Ron D, Greene LA (2002) Endoplasmic reticulum stress and the unfolded protein response in cellular models of Parkinson’s disease. J Neurosci 22:10690–10698PubMed
45.
Zurück zum Zitat Sanges D, Marigo V (2006) Cross-talk between two apoptotic pathways activated by endoplasmic reticulum stress: differential contribution of caspase-12 and AIF. Apoptosis 11:1629–1641PubMedCrossRef Sanges D, Marigo V (2006) Cross-talk between two apoptotic pathways activated by endoplasmic reticulum stress: differential contribution of caspase-12 and AIF. Apoptosis 11:1629–1641PubMedCrossRef
46.
Zurück zum Zitat Takuma K, Yan SS, Stern DM, Yamada K (2005) Mitochondrial dysfunction, endoplasmic reticulum stress, and apoptosis in Alzheimer’s disease. J Pharmacol Sci 97:312–316PubMedCrossRef Takuma K, Yan SS, Stern DM, Yamada K (2005) Mitochondrial dysfunction, endoplasmic reticulum stress, and apoptosis in Alzheimer’s disease. J Pharmacol Sci 97:312–316PubMedCrossRef
47.
Zurück zum Zitat Tang J-R, Nakamura M, Okura T, Takata Y, Watanabe S, Yang Z-H, Liu J, Kitami Y, Hiwada K (2002) Mechanism of oxidative stress-induced GADD153 gene expression in vascular smooth muscle cells. Biochem Biophys Res Commun 290:1255–1259PubMedCrossRef Tang J-R, Nakamura M, Okura T, Takata Y, Watanabe S, Yang Z-H, Liu J, Kitami Y, Hiwada K (2002) Mechanism of oxidative stress-induced GADD153 gene expression in vascular smooth muscle cells. Biochem Biophys Res Commun 290:1255–1259PubMedCrossRef
48.
Zurück zum Zitat Walter L, Hajnoczky G (2005) Mitochondria and endoplasmic reticulum: the lethal interorganelle cross-talk. J Bioenerg Biomembr 37:191–206PubMedCrossRef Walter L, Hajnoczky G (2005) Mitochondria and endoplasmic reticulum: the lethal interorganelle cross-talk. J Bioenerg Biomembr 37:191–206PubMedCrossRef
49.
Zurück zum Zitat Wang X, Wang B, Fan Z, Shi X, Ke ZJ, Luo J (20067) Thiamine deficiency induces endoplasmic reticulum stress in neurons. Neuroscience 135:1129–1139 Wang X, Wang B, Fan Z, Shi X, Ke ZJ, Luo J (20067) Thiamine deficiency induces endoplasmic reticulum stress in neurons. Neuroscience 135:1129–1139
50.
Zurück zum Zitat Wassell J, Boulton M (1997) A role for vitamin A in the formation of ocular lipofuscin. Br J Ophthalmol 81:911–918PubMedCrossRef Wassell J, Boulton M (1997) A role for vitamin A in the formation of ocular lipofuscin. Br J Ophthalmol 81:911–918PubMedCrossRef
51.
Zurück zum Zitat Yan SD, Schmidt AM, Stern D (2001) Alzheimer’s disease: inside, outside, upside down. Biochem Soc Symp 67:15–22PubMed Yan SD, Schmidt AM, Stern D (2001) Alzheimer’s disease: inside, outside, upside down. Biochem Soc Symp 67:15–22PubMed
52.
Zurück zum Zitat Yu Z, Luo H, Fu W, Mattson MP (1999) The endoplasmic reticulum stress-responsive protein GRP-78 protects neurons against excitotoxicity and apoptosis: suppression of oxidative stress and stabilization of calcium homeostasis. Exp Neurol 155:302–314PubMedCrossRef Yu Z, Luo H, Fu W, Mattson MP (1999) The endoplasmic reticulum stress-responsive protein GRP-78 protects neurons against excitotoxicity and apoptosis: suppression of oxidative stress and stabilization of calcium homeostasis. Exp Neurol 155:302–314PubMedCrossRef
53.
Zurück zum Zitat Zarbin MA (2004) Current concepts in the pathogenesis of age-related macular degeneration. Arch Ophthalmol 122:598–614PubMedCrossRef Zarbin MA (2004) Current concepts in the pathogenesis of age-related macular degeneration. Arch Ophthalmol 122:598–614PubMedCrossRef
Metadaten
Titel
Endoplasmic reticulum stress induced by oxidative stress in retinal pigment epithelial cells
verfasst von
Shikun He
Jennifer Yaung
Yeong Hoon Kim
Ernesto Barron
Stephen J. Ryan
David R. Hinton
Publikationsdatum
01.05.2008
Verlag
Springer-Verlag
Erschienen in
Graefe's Archive for Clinical and Experimental Ophthalmology / Ausgabe 5/2008
Print ISSN: 0721-832X
Elektronische ISSN: 1435-702X
DOI
https://doi.org/10.1007/s00417-008-0770-2

Weitere Artikel der Ausgabe 5/2008

Graefe's Archive for Clinical and Experimental Ophthalmology 5/2008 Zur Ausgabe

Neu im Fachgebiet Augenheilkunde

Ophthalmika in der Schwangerschaft

Die Verwendung von Ophthalmika in der Schwangerschaft und Stillzeit stellt immer eine Off-label-Anwendung dar. Ein Einsatz von Arzneimitteln muss daher besonders sorgfältig auf sein Risiko-Nutzen-Verhältnis bewertet werden. In der vorliegenden …

Operative Therapie und Keimnachweis bei endogener Endophthalmitis

Vitrektomie Originalie

Die endogene Endophthalmitis ist eine hämatogen fortgeleitete, bakterielle oder fungale Infektion, die über choroidale oder retinale Gefäße in den Augapfel eingeschwemmt wird [ 1 – 3 ]. Von dort infiltrieren die Keime in die Netzhaut, den …

Bakterielle endogene Endophthalmitis

Vitrektomie Leitthema

Eine endogene Endophthalmitis stellt einen ophthalmologischen Notfall dar, der umgehender Diagnostik und Therapie bedarf. Es sollte mit geeigneten Methoden, wie beispielsweise dem Freiburger Endophthalmitis-Set, ein Keimnachweis erfolgen. Bei der …

So erreichen Sie eine bestmögliche Wundheilung der Kornea

Die bestmögliche Wundheilung der Kornea, insbesondere ohne die Ausbildung von lichtstreuenden Narben, ist oberstes Gebot, um einer dauerhaften Schädigung der Hornhaut frühzeitig entgegenzuwirken und die Funktion des Auges zu erhalten.   

Update Augenheilkunde

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.