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Protection of Retina by Mini-αA in NaIO(3)-Induced Retinal Pigment Epithelium Degeneration Mice

Background: Studies have shown that mini-αA can protect retinal pigment epithelium (RPE) cells from apoptosis. However, no in vivo study concerning the anti-apoptotic function of mini-αA has been conducted yet. Methods: MTT assay, HE staining and TUNEL assay were used to assess levels of cells, and...

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Detalles Bibliográficos
Autores principales: Zhang, Jinglin, Zhao, Xiujuan, Cai, Yu, Li, Yonghao, Yu, Xiling, Lu, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307325/
https://www.ncbi.nlm.nih.gov/pubmed/25588217
http://dx.doi.org/10.3390/ijms16011644
Descripción
Sumario:Background: Studies have shown that mini-αA can protect retinal pigment epithelium (RPE) cells from apoptosis. However, no in vivo study concerning the anti-apoptotic function of mini-αA has been conducted yet. Methods: MTT assay, HE staining and TUNEL assay were used to assess levels of cells, and an animal model was established to examine the protective effects of mini-αA against NaIO(3)-induced RPE cell apoptosis. Western blot analysis and RT-qPCR were performed to explore the possible mechanism of mini-αA’s protective function against NaIO(3)-induced RPE cell apoptosis. Results: Results from in vivo and animal experiments showed that mini-αA antagonized NaIO(3)-induced RPE cell apoptosis. Further investigation into how mini-αA provided protection against NaIO(3)-induced RPE cell apoptosis showed that mini-αA reduced NaIO(3)-induced RPE cell apoptosis and autophagy. In addition, unfolded protein response was also involved in the protective effects of mini-αA against NaIO(3)-induced RPE cell apoptosis. Conclusions: mini-αA can antagonize RPE cell apoptosis induced by NaIO(3). A possible mechanism is by inhibition of apoptosis by repressing autophagy and endoplasmic reticulum stress.