Depletion of the Receptor-Interacting Protein Kinase 3 (RIP3) Decreases Photoreceptor Cell Death During the Early Stages of Ocular Murine Cytomegalovirus Infection

Invest Ophthalmol Vis Sci. 2018 May 1;59(6):2445-2458. doi: 10.1167/iovs.18-24086.

Abstract

Purpose: The purpose of this study was to determine if the receptor-interacting protein kinase 3 (RIP3) plays a significant role in innate immune responses and death of bystander retinal neurons during murine cytomegalovirus (MCMV) retinal infection, by comparing the innate immune response and cell death in RIP3-depleted mice (Rip3-/-) and Rip3+/+ control mice.

Methods: Rip3-/- and Rip3+/+ mice were immunosuppressed (IS) and inoculated with MCMV via the supraciliary route. Virus-injected and mock-injected control eyes were removed at days 4, 7, and 10 post infection (p.i.) and markers of innate immunity and cell death were analyzed.

Results: Compared to Rip3+/+ mice, significantly more MCMV was recovered and more MCMV-infected RPE cells were observed in injected eyes of Rip3-/- mice at days 4 and 7 p.i. In contrast, fewer TUNEL-stained photoreceptors were observed in Rip3-/- eyes than in Rip3+/+ eyes at these times. Electron microscopy showed that significantly more apoptotic photoreceptor cells were present in Rip3+/+ mice than in Rip3-/- mice. Immunohistochemistry showed that the majority of TUNEL-stained photoreceptors died via mitochondrial flavoprotein apoptosis-inducing factor (AIF)-mediated, caspase 3-independent apoptosis. The majority of RIP3-expressing cells in infected eyes were RPE cells, microglia/macrophages, and glia, whereas retinal neurons contained much lower amounts of RIP3. Western blots showed significantly higher levels of activated nuclear factor-κB and caspase 1 were present in Rip3+/+ eyes compared to Rip3-/- eyes.

Conclusions: Our results suggest that RIP3 enhances innate immune responses against ocular MCMV infection via activation of the inflammasome and nuclear factor-κB, which also leads to inflammation and death of bystander cells by multiple pathways including apoptosis and necroptosis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis*
  • Biomarkers / metabolism
  • Blotting, Western
  • Cell Survival / physiology
  • Eye Infections, Viral / metabolism
  • Eye Infections, Viral / pathology*
  • Eye Infections, Viral / virology
  • Female
  • Fluorescent Antibody Technique, Indirect
  • Herpesviridae Infections / metabolism
  • Herpesviridae Infections / pathology*
  • Herpesviridae Infections / virology
  • Immunity, Innate / physiology
  • In Situ Nick-End Labeling
  • Inflammasomes / immunology
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Microscopy, Electron
  • Muromegalovirus / isolation & purification*
  • NF-kappa B / metabolism
  • Photoreceptor Cells, Vertebrate / pathology*
  • Receptor-Interacting Protein Serine-Threonine Kinases / physiology*
  • Retinal Diseases / metabolism
  • Retinal Diseases / pathology*
  • Retinal Diseases / virology
  • Retinal Pigment Epithelium / virology

Substances

  • Biomarkers
  • Inflammasomes
  • NF-kappa B
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Ripk3 protein, mouse