Retinal cell death caused by sodium iodate involves multiple caspase-dependent and caspase-independent cell-death pathways

14Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

© 2015 by the authors; licensee MDPI, Basel, Switzerland.Herein, we have investigated retinal cell-death pathways in response to the retina toxin sodium iodate (NaIO<inf>3</inf>) both in vivo and in vitro. C57/BL6 mice were treated with a single intravenous injection of NaIO<inf>3</inf> (35 mg/kg). Morphological changes in the retina post NaIO<inf>3</inf> injection in comparison to untreated controls were assessed using electron microscopy. Cell death was determined by TdT-mediated dUTP-biotin nick end labeling (TUNEL) staining. The activation of caspases and calpain was measured using immunohistochemistry. Additionally, cytotoxicity and apoptosis in retinal pigment epithelial (RPE) cells, primary retinal cells, and the cone photoreceptor (PRC) cell line 661W were assessed in vitro after NaIO<inf>3</inf> treatment using the ApoToxGlo™ assay. The 7-AAD/Annexin-V staining was performed and necrostatin (Nec-1) was administered to the NaIO<inf>3</inf>-treated cells to confirm the results. In vivo, degenerating RPE cells displayed a rounded shape and retracted microvilli, whereas PRCs featured apoptotic nuclei. Caspase and calpain activity was significantly upregulated in retinal sections and protein samples from NaIO<inf>3</inf>-treated animals. In vitro, NaIO<inf>3</inf> induced necrosis in RPE cells and apoptosis in PRCs. Furthermore, Nec-1 significantly decreased NaIO<inf>3</inf>-induced RPE cell death, but had no rescue effect on treated PRCs. In summary, several different cell-death pathways are activated in retinal cells as a result of NaIO<inf>3</inf>.

Cite

CITATION STYLE

APA

Balmer, J., Zulliger, R., Roberti, S., & Enzmann, V. (2015). Retinal cell death caused by sodium iodate involves multiple caspase-dependent and caspase-independent cell-death pathways. International Journal of Molecular Sciences, 16(7), 15086–15103. https://doi.org/10.3390/ijms160715086

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free