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Nrf‐2 and PGC 1‐alpha deletion affects ultrastructural changes in retinal pigmented epithelium associated with the changes of oxidative stress and autophagy markers expression pattern in compound null mice
Author(s) -
Kivinen N.,
Viiri J.,
Koskela A.,
Kettunen M.,
Koistinen A.,
Winiarczyk M.,
Kauppinen A.,
Kaarniranta K.,
Felszeghy S.
Publication year - 2017
Publication title -
acta ophthalmologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.534
H-Index - 87
eISSN - 1755-3768
pISSN - 1755-375X
DOI - 10.1111/j.1755-3768.2017.0t002
Subject(s) - autophagy , retinal pigment epithelium , oxidative stress , retinal , biology , downregulation and upregulation , microbiology and biotechnology , pathology , ex vivo , retinal degeneration , in vivo , endocrinology , medicine , apoptosis , genetics , biochemistry , gene
Purpose There is increasing evidence that NF ‐E2‐related factor 2 (Nrf‐2) and peroxisome proliferator‐activated receptor‐gamma coactivator 1‐alpha ( PGC ‐1 α ) participate in age‐related retinal degeneration process. Our study aimed to provide de novo, in and ex vivo high‐resolution imaging of eyes from different degenerative mouse models mimicking cellular changes observed in aged retinal pigmented epithelium ( RPE ). Methods The gross morphological alterations of eyes were analyzed by in vivo micro MRI . Oxidative stress marker (4‐ HNE ) and the autophagy regulators (p62/ SQSTM 1, Beclin‐1, LC 3, Ubiquitin) were examined on thin wax sections by highly specific immunohistochemistry using semi‐quantitative computer aided image analysis. Moreover accurate transmission electron microscopy ultrastructural assay was carried out to monitor the organelle changes in the RPE obtained from Nrf‐2/ PGC ‐1 α knockout mice. Results Collectively, age‐related autophagy decline and mitochondrial dysfunction was recorded in the RPE joined with upregulation of stress related biomarkers. Conclusions Taken together, our experimental data highlight for the first time that common deletion of Nrf‐2 and PGC ‐1 α might appear to have potential and broad applicability for retinal aging research.