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Autophagy protects against retinal cell death in mouse model of cytomegalovirus retinitis
Juan Mo1,2, Sally S Atherton3, Liya Wang4
1Henan Eye Institute, Henan Eye Hospital, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, Henan Province, 450003, People's Republic of China. mojuan52@gmail.com.
Background:
Extensive death of uninfected bystander neuronal cells is an important component of the pathogenesis of cytomegalovirus retinitis (CMV). Our previous results have shown that there is a functional relationship between autophagy and apoptosis during MCMV infection of retinal pigment epithelium (RPE). The purpose of this study was to determine whether autophagy plays a significant role in the death of retinal cells during MCMV retinitis.
Methods:
The retinas of adult BALB/c mice were infected with MCMV via supraciliary injection. Rapamycin, a mTOR inhibitor, was injected to MCMV-infected BALB/c mice intraperitoneally. Immunohistochemistry and western blot were performed to observe the spread pattern of virus in retinas and the levels of targeted proteins. Plaque assay was performed to determine the virus titer in different groups. Since Atg5 is a key gene regulating autophagy, we bred Atg5flox/flox; Nestin-Cre mice to deeply elucidate the role of autophagy during MCMV retinitis. Atg5flox/flox; Nestin-Cre mice were genotyped and infected with MCMV. Immunohistochemistry was performed to observe the type of virus-infected cells and apoptosis in retinas during MCMV retinitis.
Results:
In MCMV mouse model, MCMV infection in outer nuclear layer (ONL) and inner nuclear layer (INL) in the retinas caused cleaved caspase 3 positive apoptosis, which is not co-localized with early antigen (EA) positive virus infected cells in rapamycin treated group. Rapamycin treatment increased the levels of LC3B-II by inhibiting mTOR and decreased the levels of cleaved caspase-3 during MCMV retinitis. However, virus propagation was not affected by rapamycin. In Atg5flox/flox; Nestin-Cre mice, RPE and glial cells were the main targets of viral infection, and number of EA positive retinal cells and TUNEL positive retinal cells was significantly increased compared to Atg5flox/+; Nestin-Cre mice though there was no difference of virus propagation between Atg5flox/flox; Nestin-Cre mice and Atg5flox/+; Nestin-Cre mice.
Conclusions:
Autophagy protects retinal cells from MCMV infection induced apoptosis through mTOR-mediated signaling pathway.
Insights
Autophagy protects retinal cells from cytomegalovirus retinitis (CMV) by reducing apoptosis. Inhibiting mTOR with rapamycin decreased cell death, while blocking autophagy increased it, highlighting autophagy's protective role in CMV infection.
Area of Science:
- Ophthalmology
- Virology
- Cell Biology
Background:
- Cytomegalovirus retinitis (CMV) causes significant death of uninfected bystander retinal cells.
- Previous studies indicated a link between autophagy and apoptosis in cytomegalovirus-infected retinal pigment epithelium (RPE).
Purpose of the Study:
- To investigate the role of autophagy in retinal cell death during cytomegalovirus retinitis (CMV).
Main Methods:
- Murine cytomegalovirus (MCMV) infection model in BALB/c mice.
- Administration of rapamycin (mTOR inhibitor) and genetic manipulation of autophagy-related gene 5 (Atg5).
- Immunohistochemistry, Western blot, and plaque assays to assess viral spread, protein levels, and cell apoptosis.
Main Results:
- Rapamycin treatment inhibited mTOR, increased autophagy marker LC3B-II, and reduced apoptosis (cleaved caspase-3) without affecting viral propagation.
- In mice with Atg5 deletion, retinal pigment epithelium and glial cells showed increased viral and apoptotic markers, despite similar viral loads compared to control mice.
Conclusions:
- Autophagy plays a protective role against apoptosis induced by cytomegalovirus (CMV) infection in retinal cells.
- The mTOR-mediated signaling pathway is involved in regulating autophagy's protective effect during CMV retinitis.
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