The Effect of A2E on the Ca2+-PKC Signaling Pathway in Human RPE Cells Exposed to Blue Light

被引:4
作者
Luo, Maomei [1 ,2 ,3 ]
Wang, Shu [1 ,3 ]
Tang, Yun [3 ]
Zeng, Chun [1 ,3 ]
Cai, Shanjun [1 ,3 ]
机构
[1] Zunyi Med Univ, Guizhou Eye Hosp, Dept Ophthalmol, Affiliated Hosp, Zunyi, Guizhou, Peoples R China
[2] Dazhou Cent Hosp, Dept Ophthalmol, Dazhou, Sichuan, Peoples R China
[3] Zunyi Med Univ, Zunyi, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
RETINAL-PIGMENT EPITHELIUM; DYSREGULATION; LIPOFUSCIN; INTEGRITY; LYSOSOME; DAMAGE;
D O I
10.1155/2022/2233223
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Aims. In a model of blue light-induced damage in N-retinylidene-N-retinylethanolamine (A2E)-loaded human retinal pigment epithelial (RPE) cells, we examined the effect of A2E on the calcium (Ca2+)-protein kinase C (PKC) signaling pathway. Methods. Primary human RPE cells were cultured, and the cells in the 4th-6th passages were used in this study. The cells were divided into 5 groups: control cells (no A2E, no blue light), blue light-treated cells, blue light + chloroquine-treated cells, blue light + A2E-treated cells, and blue light + A2E + chloroquine-treated cells. The cells were first treated with chloroquine (15 mu M for 12 h) and then loaded with A2E (25 mu M for 2 h).The blue light intensity was 2000 & PLUSMN; 500 lux, and the duration was 6 h. After blue light exposure, the cells were cultured for 24 h. Fluo-3/AM staining was used to determine the level of cytoplasmic Ca2+, and the cells were photographed using a laser scanning confocal microscope to analyze the fluorescence intensity. The intracellular levels of inositol triphosphate (IP3) and diacylglycerol (DAG) were measured by enzyme-linked immunosorbent assay (ELISA). Intracellular PKC activity was measured with a nonradioactive nuclide assay. Results. Among all cell groups, the levels of Ca2+, DAG, and IP3 were lowest in the control cells (P < 0.05). The Ca2+, DAG, and IP3 levels in the blue light + A2E-treated cells and blue light + chloroquine-treated cells were higher than those in the blue light-treated cells (P < 0.05). The Ca2+, DAG, and IP3 levels were highest in the blue light + A2E + chloroquine-treated group (P < 0.05). PKC activity was lowest in the control cells (P < 0.05). The PKC activity of the blue light + A2E-treated cells and blue light + chloroquine-treated cells was higher than that of the blue light-treated cells (P < 0.05), and the PKC activity of the blue light + A2E + chloroquine-treated cells was the highest (P < 0.05). Conclusion. Blue light and A2E increased the levels of Ca2+, IP3, and DAG in human RPE cells and enhanced PKC activity, and blue light and A2E had a synergistic effect. Chloroquine further increased the levels of Ca2+, IP3, and DAG and PKC activity in RPE cells or A2E-loaded RPE cells exposed to blue light.
引用
收藏
页数:7
相关论文
共 49 条
[21]   RAR Inhibitors Display Photo-Protective and Anti-Inflammatory Effects in A2E Stimulated RPE Cells In Vitro through Non-Specific Modulation of PPAR or RXR Transactivation [J].
Fontaine, Valerie ;
Boumedine, Thinhinane ;
Monteiro, Elodie ;
Fournie, Mylene ;
Gersende, Gendre ;
Sahel, Jose-Alain ;
Picaud, Serge ;
Veillet, Stanislas ;
Lafont, Rene ;
Latil, Mathilde ;
Dilda, Pierre J. ;
Camelo, Serge .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (05)
[22]   Comparative study of the dark and light-induced toxicity of lipofuscin granules from human retinal pigment epithelium and their chromophore A2E on the cardiolipin liposome model [J].
Dontsov, A. E. ;
Sakina, N. L. ;
Ostrovsky, M. A. .
RUSSIAN CHEMICAL BULLETIN, 2012, 61 (02) :442-448
[23]   Luteolin protects human ARPE-19 retinal pigment epithelium cells from blue light-induced phototoxicity through activation of Nrf2/Keap1 signaling [J].
Hayakawa, Ryo ;
Ishii, Takeshi ;
Fushimi, Taiki ;
Kamei, Yuki ;
Yamaguchi, Ai ;
Sugimoto, Kenji ;
Ashida, Hitoshi ;
Akagawa, Mitsugu .
FREE RADICAL RESEARCH, 2025, 59 (04) :356-368
[24]   The Effect of Shikonin on U87 Cells Through Notch2 Signaling Pathway and Its Mechanism [J].
Yuan, Lei ;
Zhang, Ting ;
Pan, Hong ;
Wang, Fei .
JOURNAL OF BIOMATERIALS AND TISSUE ENGINEERING, 2021, 11 (02) :290-294
[25]   Anti-apoptotic effects of Curcuma longa L. extract and its curcuminoids against blue light-induced cytotoxicity in A2E-laden human retinal pigment epithelial cells [J].
Park, Sang-il ;
Lee, Eun Hye ;
Kim, So Ra ;
Jang, Young Pyo .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2017, 69 (03) :334-340
[26]   Bis-Retinoid A2E Induces an Increase of Basic Fibroblast Growth Factor via Inhibition of Extracellular Signal-Regulated Kinases 1/2 Pathway in Retinal Pigment Epithelium Cells and Facilitates Phagocytosis.2 [J].
Balmer, Delphine ;
Bapst-Wicht, Linda ;
Pyakurel, Aswin ;
Emery, Martine ;
Nanchen, Natacha ;
Bochet, Christian G. ;
Roduit, Raphael .
FRONTIERS IN AGING NEUROSCIENCE, 2017, 9
[27]   Toxic effects of A2E in human ARPE-19 cells were prevented by resveratrol: a potential nutritional bioactive for age-related macular degeneration treatment [J].
Alaimo, Agustina ;
Carolina Di Santo, Mariana ;
Dominguez Rubio, Ana Paula ;
Chaufan, Gabriela ;
Garcia Linares, Guadalupe ;
Edgardo Perez, Oscar .
ARCHIVES OF TOXICOLOGY, 2020, 94 (02) :553-572
[28]   Protective Effects of Dipterocarpus tuberculatus in Blue Light-Induced Macular Degeneration in A2E-Laden ARPE19 Cells and Retina of Balb/c Mice [J].
Lee, Su Jin ;
Roh, Yu Jeong ;
Kim, Ji Eun ;
Jin, You Jeong ;
Song, Hee Jin ;
Seol, Ayun ;
Park, So Hae ;
Douangdeuane, Bounleuane ;
Souliya, Onevilay ;
Choi, Sun Il ;
Hwang, Dae Youn .
ANTIOXIDANTS, 2023, 12 (02)
[29]   A novel fluorescence-based assay for measuring A2E removal from human retinal pigment epithelial cells to screen for age-related macular degeneration inhibitors [J].
Jin, Hong Lan ;
Lee, Sung-Chan ;
Kwon, Yong Sam ;
Choung, Se-Young ;
Jeong, Kwang Won .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2016, 117 :560-567
[30]   Fucoidan protects ARPE-19 cells from oxidative stress via normalization of reactive oxygen species generation through the Ca2+-dependent ERK signaling pathway [J].
Li, Xiaoxia ;
Zhao, Haiyan ;
Wang, Qingfa ;
Liang, Hongyan ;
Jiang, Xiaofeng .
MOLECULAR MEDICINE REPORTS, 2015, 11 (05) :3746-3752