Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons

Metabolite profiling is an important tool that may better capture the multiple features of neurodegeneration. With the considerable parallels between mouse and human metabolism, the use of metabolomics in mouse models with neurodegenerative pathology provides mechanistic insight and ready translatio...

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Main Authors: Geiszler, Philippine C., Ugun-Klusek, Aslihan, Lawler, Karen, Pardon, Marie-Christine, Yuchun, Ding, Bai, Li, Daykin, Clare, Auer, Dorothee P., Bedford, Lynn
Format: Article
Language:English
Published: Nature Publishing Group 2018
Online Access:https://eprints.nottingham.ac.uk/50317/
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author Geiszler, Philippine C.
Ugun-Klusek, Aslihan
Lawler, Karen
Pardon, Marie-Christine
Yuchun, Ding
Bai, Li
Daykin, Clare
Auer, Dorothee P.
Bedford, Lynn
author_facet Geiszler, Philippine C.
Ugun-Klusek, Aslihan
Lawler, Karen
Pardon, Marie-Christine
Yuchun, Ding
Bai, Li
Daykin, Clare
Auer, Dorothee P.
Bedford, Lynn
author_sort Geiszler, Philippine C.
building Nottingham Research Data Repository
collection Online Access
description Metabolite profiling is an important tool that may better capture the multiple features of neurodegeneration. With the considerable parallels between mouse and human metabolism, the use of metabolomics in mouse models with neurodegenerative pathology provides mechanistic insight and ready translation into aspects of human disease. Using 400 MHz nuclear magnetic resonance spectroscopy we have carried out a temporal region-specific investigation of the metabolome of neuron-specific 26S proteasome knockout mice characterised by progressive neurodegeneration and Lewy-like inclusion formation in the forebrain. An early significant decrease in N-acetyl aspartate revealed evidence of neuronal dysfunction before cell death that may be associated with changes in brain neuroenergetics, underpinning the use of this metabolite to track neuronal health. Importantly, we show early and extensive activation of astrocytes and microglia in response to targeted neuronal dysfunction in this context, but only late changes in myo-inositol; the best established glial cell marker in magnetic resonance spectroscopy studies, supporting recent evidence that additional early neuroinflammatory markers are needed. Our results extend the limited understanding of metabolite changes associated with gliosis and provide evidence that changes in glutamate homeostasis and lactate may correlate with astrocyte activation and have biomarker potential for tracking neuroinflammation.
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spelling nottingham-503172020-05-08T09:30:11Z https://eprints.nottingham.ac.uk/50317/ Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons Geiszler, Philippine C. Ugun-Klusek, Aslihan Lawler, Karen Pardon, Marie-Christine Yuchun, Ding Bai, Li Daykin, Clare Auer, Dorothee P. Bedford, Lynn Metabolite profiling is an important tool that may better capture the multiple features of neurodegeneration. With the considerable parallels between mouse and human metabolism, the use of metabolomics in mouse models with neurodegenerative pathology provides mechanistic insight and ready translation into aspects of human disease. Using 400 MHz nuclear magnetic resonance spectroscopy we have carried out a temporal region-specific investigation of the metabolome of neuron-specific 26S proteasome knockout mice characterised by progressive neurodegeneration and Lewy-like inclusion formation in the forebrain. An early significant decrease in N-acetyl aspartate revealed evidence of neuronal dysfunction before cell death that may be associated with changes in brain neuroenergetics, underpinning the use of this metabolite to track neuronal health. Importantly, we show early and extensive activation of astrocytes and microglia in response to targeted neuronal dysfunction in this context, but only late changes in myo-inositol; the best established glial cell marker in magnetic resonance spectroscopy studies, supporting recent evidence that additional early neuroinflammatory markers are needed. Our results extend the limited understanding of metabolite changes associated with gliosis and provide evidence that changes in glutamate homeostasis and lactate may correlate with astrocyte activation and have biomarker potential for tracking neuroinflammation. Nature Publishing Group 2018-03-19 Article PeerReviewed application/pdf en cc_by https://eprints.nottingham.ac.uk/50317/8/Mouse%20s41598-018-23155-2.pdf Geiszler, Philippine C., Ugun-Klusek, Aslihan, Lawler, Karen, Pardon, Marie-Christine, Yuchun, Ding, Bai, Li, Daykin, Clare, Auer, Dorothee P. and Bedford, Lynn (2018) Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons. Scientific Reports, 8 . 4833/1-4833/13. ISSN 2045-2322 http://www.nature.com/articles/s41598-018-23155-2 doi:10.1038/s41598-018-23155-2 doi:10.1038/s41598-018-23155-2
spellingShingle Geiszler, Philippine C.
Ugun-Klusek, Aslihan
Lawler, Karen
Pardon, Marie-Christine
Yuchun, Ding
Bai, Li
Daykin, Clare
Auer, Dorothee P.
Bedford, Lynn
Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons
title Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons
title_full Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons
title_fullStr Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons
title_full_unstemmed Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons
title_short Dynamic metabolic patterns tracking neurodegeneration and gliosis following 26S proteasome dysfunction in mouse forebrain neurons
title_sort dynamic metabolic patterns tracking neurodegeneration and gliosis following 26s proteasome dysfunction in mouse forebrain neurons
url https://eprints.nottingham.ac.uk/50317/
https://eprints.nottingham.ac.uk/50317/
https://eprints.nottingham.ac.uk/50317/