Age-related distribution and potential role of SNCB in topographically different retinal areas of the common marmoset Callithrix jacchus, including the macula.
Aging
/ physiology
Animals
Apoptosis
Callithrix
Cell Line
Cells, Cultured
Dose-Response Relationship, Drug
Female
Gene Expression Regulation
/ physiology
Heme Oxygenase (Decyclizing)
/ metabolism
Humans
Male
NADPH Oxidase 4
/ metabolism
Oxidative Stress
Paraffin Embedding
Proto-Oncogene Proteins c-mdm2
/ genetics
RNA, Messenger
/ genetics
Real-Time Polymerase Chain Reaction
Retina
/ drug effects
Retinal Pigment Epithelium
/ drug effects
Signal Transduction
Sus scrofa
Tumor Suppressor Protein p53
/ genetics
beta-Synuclein
/ metabolism
Age-related macular degeneration
Aging
Beta-synuclein
Callithrix jacchus
RPE
Journal
Experimental eye research
ISSN: 1096-0007
Titre abrégé: Exp Eye Res
Pays: England
ID NLM: 0370707
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
07
12
2018
revised:
08
04
2019
accepted:
21
05
2019
pubmed:
28
5
2019
medline:
15
2
2020
entrez:
26
5
2019
Statut:
ppublish
Résumé
Evidence of an age-related increase of β-synuclein (SNCB) in several parts of the visual system including the retina has been reported. SNCB is thought to function as an antagonist of α-synuclein in neurodegenerative diseases, but the exact role of SNCB remains unclear. The presented work studies two different aspects of the onset and role of SNCB in the retinal pigment epithelium (RPE). First, the topographical and intracellular distributions of SNCB in the RPE of non-human marmoset monkey (Callithrix jacchus) were evaluated in paraffin-embedded eyes and RPE whole mounts from different developmental stages (neonatal, adolescent, and adult). Thus, revealed distinct lifetime-related alterations of the topographical and intracellular distributions of SNCB in the primate macula compared to the retinal periphery. Furthermore, the function and influences of SNCB on ARPE-19 cells and primary porcine RPE (ppRPE) cells were characterized by exposing these cells with recombinant SNCB (rSNCB) at different concentrations. Moreover, apoptosis, protein- and mRNA-expression levels of factors of the p53/MDM2 signaling cascade and inflammation- and oxidation-related genes were investigated. The observed dose-depended decreased apoptosis rates together with the PLD2 mediated activation of the p53 pathway promotes senescence-related processes in SNCB exposed common ARPE-19 cells from human origin. Further, increased HMOX1 and NOX4 levels indicate increased oxidative stress and inflammatory responses triggered by SNCB. The obtained differences in the distribution of SNCB in primate RPE together with alterations of cellular functions in rSNCB-exposed RPE cells (e.g., ARPE-19, ppRPE) support SNCB-related effects like inflammatory response and stress-related properties on RPE over lifetime. The possible functional relevance of SNCB in physiological aging converting into a pathophysiological condition should be investigated in further studies.
Identifiants
pubmed: 31128101
pii: S0014-4835(18)30897-2
doi: 10.1016/j.exer.2019.05.016
pii:
doi:
Substances chimiques
RNA, Messenger
0
Tumor Suppressor Protein p53
0
beta-Synuclein
0
Heme Oxygenase (Decyclizing)
EC 1.14.14.18
NADPH Oxidase 4
EC 1.6.3.-
Proto-Oncogene Proteins c-mdm2
EC 2.3.2.27
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
107676Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.