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Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress

Photoreceptor death is the ultimate cause of vision loss in many retinal degenerative conditions. Identifying novel therapeutic avenues for prolonging photoreceptor health and function has the potential to improve vision and quality of life for patients suffering from degenerative retinal disorders....

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Autores principales: Weh, Eric, Lutrzykowska, Zuzanna, Smith, Andrew, Hager, Heather, Pawar, Mercy, Wubben, Thomas J., Besirli, Cagri G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272456/
https://www.ncbi.nlm.nih.gov/pubmed/32499533
http://dx.doi.org/10.1038/s41419-020-2638-2
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author Weh, Eric
Lutrzykowska, Zuzanna
Smith, Andrew
Hager, Heather
Pawar, Mercy
Wubben, Thomas J.
Besirli, Cagri G.
author_facet Weh, Eric
Lutrzykowska, Zuzanna
Smith, Andrew
Hager, Heather
Pawar, Mercy
Wubben, Thomas J.
Besirli, Cagri G.
author_sort Weh, Eric
collection PubMed
description Photoreceptor death is the ultimate cause of vision loss in many retinal degenerative conditions. Identifying novel therapeutic avenues for prolonging photoreceptor health and function has the potential to improve vision and quality of life for patients suffering from degenerative retinal disorders. Photoreceptors are metabolically unique among other neurons in that they process the majority of their glucose via aerobic glycolysis. One of the main regulators of aerobic glycolysis is hexokinase 2 (HK2). Beyond its enzymatic function of phosphorylating glucose to glucose-6-phosphate, HK2 has additional non-enzymatic roles, including the regulation of apoptotic signaling via AKT signaling. Determining the role of HK2 in photoreceptor homeostasis may identify novel signaling pathways that can be targeted with neuroprotective agents to boost photoreceptor survival during metabolic stress. Here we show that following experimental retinal detachment, p-AKT is upregulated and HK2 translocates to mitochondria. Inhibition of AKT phosphorylation in 661W photoreceptor-like cells results in translocation of mitochondrial HK2 to the cytoplasm, increased caspase activity, and decreased cell viability. Rod-photoreceptors lacking HK2 upregulate HK1 and appear to develop normally. Interestingly, we found that HK2-deficient photoreceptors are more susceptible to acute nutrient deprivation in the experimental retinal detachment model. Additionally, HK2 appears to be important for preserving photoreceptors during aging. We show that retinal glucose metabolism is largely unchanged after HK2 deletion, suggesting that the non-enzymatic role of HK2 is important for maintaining photoreceptor health. These results suggest that HK2 expression is critical for preserving photoreceptors during acute nutrient stress and aging. More specifically, p-AKT mediated translocation of HK2 to the mitochondrial surface may be critical for protecting photoreceptors from acute and chronic stress.
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spelling pubmed-72724562020-06-15 Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress Weh, Eric Lutrzykowska, Zuzanna Smith, Andrew Hager, Heather Pawar, Mercy Wubben, Thomas J. Besirli, Cagri G. Cell Death Dis Article Photoreceptor death is the ultimate cause of vision loss in many retinal degenerative conditions. Identifying novel therapeutic avenues for prolonging photoreceptor health and function has the potential to improve vision and quality of life for patients suffering from degenerative retinal disorders. Photoreceptors are metabolically unique among other neurons in that they process the majority of their glucose via aerobic glycolysis. One of the main regulators of aerobic glycolysis is hexokinase 2 (HK2). Beyond its enzymatic function of phosphorylating glucose to glucose-6-phosphate, HK2 has additional non-enzymatic roles, including the regulation of apoptotic signaling via AKT signaling. Determining the role of HK2 in photoreceptor homeostasis may identify novel signaling pathways that can be targeted with neuroprotective agents to boost photoreceptor survival during metabolic stress. Here we show that following experimental retinal detachment, p-AKT is upregulated and HK2 translocates to mitochondria. Inhibition of AKT phosphorylation in 661W photoreceptor-like cells results in translocation of mitochondrial HK2 to the cytoplasm, increased caspase activity, and decreased cell viability. Rod-photoreceptors lacking HK2 upregulate HK1 and appear to develop normally. Interestingly, we found that HK2-deficient photoreceptors are more susceptible to acute nutrient deprivation in the experimental retinal detachment model. Additionally, HK2 appears to be important for preserving photoreceptors during aging. We show that retinal glucose metabolism is largely unchanged after HK2 deletion, suggesting that the non-enzymatic role of HK2 is important for maintaining photoreceptor health. These results suggest that HK2 expression is critical for preserving photoreceptors during acute nutrient stress and aging. More specifically, p-AKT mediated translocation of HK2 to the mitochondrial surface may be critical for protecting photoreceptors from acute and chronic stress. Nature Publishing Group UK 2020-06-04 /pmc/articles/PMC7272456/ /pubmed/32499533 http://dx.doi.org/10.1038/s41419-020-2638-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Weh, Eric
Lutrzykowska, Zuzanna
Smith, Andrew
Hager, Heather
Pawar, Mercy
Wubben, Thomas J.
Besirli, Cagri G.
Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress
title Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress
title_full Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress
title_fullStr Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress
title_full_unstemmed Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress
title_short Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress
title_sort hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272456/
https://www.ncbi.nlm.nih.gov/pubmed/32499533
http://dx.doi.org/10.1038/s41419-020-2638-2
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