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KMID : 0620920210530111748
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Experimental & Molecular Medicine
2021 Volume.53 No. 11 p.1748 ~ p.1758
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Muller glial responses compensate for degenerating photoreceptors in retinitis pigmentosa
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Tomita Yohei
Qiu Chenxi
Bull Edward
Allen William
Kotoda Yumi
Talukdar Saswata
Smith Lois E. H.
Fu Zhongjie
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Abstract
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Photoreceptor degeneration caused by genetic defects leads to retinitis pigmentosa, a rare disease typically diagnosed in adolescents and young adults. In most cases, rod loss occurs first, followed by cone loss as well as altered function in cells connected to photoreceptors directly or indirectly. There remains a gap in our understanding of retinal cellular responses to photoreceptor abnormalities. Here, we utilized single-cell transcriptomics to investigate cellular responses in each major retinal cell type in retinitis pigmentosa model (P23H) mice vs. wild-type littermate mice. We found a significant decrease in the expression of genes associated with phototransduction, the inner/outer segment, photoreceptor cell cilium, and photoreceptor development in both rod and cone clusters, in line with the structural changes seen with immunohistochemistry. Accompanying this loss was a significant decrease in the expression of genes involved in metabolic pathways and energy production in both rods and cones. We found that in the Muller glia/astrocyte cluster, there was a significant increase in gene expression in pathways involving photoreceptor maintenance, while concomitant decreases were observed in rods and cones. Additionally, the expression of genes involved in mitochondrial localization and transport was increased in the Muller glia/astrocyte cluster. The Muller glial compensatory increase in the expression of genes downregulated in photoreceptors suggests that Muller glia adapt their transcriptome to support photoreceptors and could be thought of as general therapeutic targets to protect against retinal degeneration.
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KEYWORD
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Experimental models of disease, Retina
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