Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
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. |
---|