Resveratrol as Inducer of Autophagy, Pro-Survival, and Anti-Inflammatory Stimuli in Cultured Human RPE Cells.

Purpose: To investigate the mechanism by which resveratrol acts upon retinal pigment epithelial (RPE) cells and to characterize its effect upon autophagy, survival, and inflammation, with consequent implications to treatment for age-related macular degeneration (AMD).Cultured ARPE-19 cells were expo...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Josifovska Natasha
Albert Réka
Nagymihály Richárd
Lytvynchuk Lyubomyr
Moe Morten C.
Kaarniranta Kai
Veréb Zoltán
Petrovski Goran
Dokumentumtípus: Cikk
Megjelent: 2020
Sorozat:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 21 No. 3
doi:10.3390/ijms21030813

mtmt:31181119
Online Access:http://publicatio.bibl.u-szeged.hu/18312
LEADER 03090nab a2200289 i 4500
001 publ18312
005 20200228092846.0
008 200228s2020 hu o 0|| zxx d
022 |a 1661-6596 
024 7 |a 10.3390/ijms21030813  |2 doi 
024 7 |a 31181119  |2 mtmt 
040 |a SZTE Publicatio Repozitórium  |b hun 
041 |a zxx 
100 1 |a Josifovska Natasha 
245 1 0 |a Resveratrol as Inducer of Autophagy, Pro-Survival, and Anti-Inflammatory Stimuli in Cultured Human RPE Cells.  |h [elektronikus dokumentum] /  |c  Josifovska Natasha 
260 |c 2020 
300 |a Azonosító: 813-Terjedelem: 12 p 
490 0 |a INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES  |v 21 No. 3 
520 3 |a Purpose: To investigate the mechanism by which resveratrol acts upon retinal pigment epithelial (RPE) cells and to characterize its effect upon autophagy, survival, and inflammation, with consequent implications to treatment for age-related macular degeneration (AMD).Cultured ARPE-19 cells were exposed to 10 and 50 μM resveratrol. Cell survival/death was determined by annexin-FITC/propidium iodide using flow cytometry, while autophagy was studied by detecting autophagic vacuoles formation (acridine orange and transmission electron microscopy), as well as LC3II/I ratio and p62 expression by Western blot. In addition, time-lapse confocal microscopy of a pDENDRA-LC3 expression vector was performed to detect autophagy in transfected ARPE-19 cells under the different treatment conditions. Inhibition of proteasomal and autophagy-lysosomal fusion was carried out by MG-132 and chloroquine, respectively, while induction of autophagy was achieved by rapamycin treatment. Detection of secreted cytokines by ARPE-19 cells using Human XL Cytokine Array was performed under oxidative stress (H2O2) and resveratrol treatments, respectively.Resveratrol induced autophagy in ARPE-19 cells as determined by augmented presence of autophagic vacuoles, increased LC3II/I ratio and decreased p62 expression, as well as time-lapse confocal microscopy using pDENDRA-LC3 expression vector. Resveratrol acted similarly to proteasomal inhibition and downstream of mammalian target of rapamycin (mTOR), since upstream inhibition of autophagy by 3-methyladenine could not inhibit autophagy in ARPE-19 cells. Co-treatmeant by rapamycin and/or proteasome inhibition showed no additive effect upon autophagy induction. ARPE-19 cells treated by resveratrol showed lower cell death rate compared to untreated controls. Resveratrol induced a specific anti-inflammatory response in ARPE-19 cells.Resveratrol can induce autophagy, pro-survival, and anti-inflammatory stimuli in ARPE-19 cells, properties which could be plausible to formulate future treatment modalities for AMD. 
700 0 1 |a Albert Réka  |e aut 
700 0 1 |a Nagymihály Richárd  |e aut 
700 0 1 |a Lytvynchuk Lyubomyr  |e aut 
700 0 1 |a Moe Morten C.  |e aut 
700 0 1 |a Kaarniranta Kai  |e aut 
700 0 1 |a Veréb Zoltán  |e aut 
700 0 1 |a Petrovski Goran  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/18312/1/ijms-21-00813-v21.pdf  |z Dokumentum-elérés