4.7 Article

SARM1 Ablation Is Protective and Preserves Spatial Vision in an In Vivo Mouse Model of Retinal Ganglion Cell Degeneration

Journal

Publisher

MDPI
DOI: 10.3390/ijms23031606

Keywords

axon degeneration; sterile alpha and Toll; interleukin-1 receptor motif-containing 1 (SARM1); NAD plus; NADase; retinal degeneration

Ask authors/readers for more resources

The challenge of developing gene therapies for genetic forms of blindness is heightened by the heterogeneity of these conditions. However, mechanistic commonalities indicate key pathways that may be targeted in a gene-independent approach. This study explores the neuroprotective effect of SARM1 ablation in a mouse model of retinal ganglion cell loss and visual dysfunction induced by rotenone. The results show that Sarm1 knockout mice retain visual function after rotenone insult and have significantly higher optokinetic response measurements than wild type mice. The protection of spatial vision is sustained over time and is accompanied by increased RGC survival and preservation of axonal density in the optic nerves. Fibroblasts from Sarm1 knockout mice demonstrate increased mitochondrial bioenergetics. These findings suggest that SARM1 ablation can increase mitochondrial function and provide histological and functional protection against mitochondrial dysfunction in the mouse retina.
The challenge of developing gene therapies for genetic forms of blindness is heightened by the heterogeneity of these conditions. However, mechanistic commonalities indicate key pathways that may be targeted in a gene-independent approach. Mitochondrial dysfunction and axon degeneration are common features of many neurodegenerative conditions including retinal degenerations. Here we explore the neuroprotective effect afforded by the absence of sterile alpha and Toll/interleukin-1 receptor motif-containing 1 (SARM1), a prodegenerative NADase, in a rotenone-induced mouse model of retinal ganglion cell loss and visual dysfunction. Sarm1 knockout mice retain visual function after rotenone insult, displaying preservation of photopic negative response following rotenone treatment in addition to significantly higher optokinetic response measurements than wild type mice following rotenone. Protection of spatial vision is sustained over time in both sexes and is accompanied by increased RGC survival and additionally preservation of axonal density in optic nerves of Sarm1(-/-) mice insulted with rotenone. Primary fibroblasts extracted from Sarm1(-/-) mice demonstrate an increased oxygen consumption rate relative to those from wild type mice, with significantly higher basal, maximal and spare respiratory capacity. Collectively, our data indicate that Sarm1 ablation increases mitochondrial bioenergetics and confers histological and functional protection in vivo in the mouse retina against mitochondrial dysfunction, a hallmark of many neurodegenerative conditions including a variety of ocular disorders.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available