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Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling
Astrocyte activation is a common feature of neurodegenerative diseases. However, the ways in which dying neurons influence the activity of astrocytes is poorly understood. RIPK3 signaling has recently been described as a key regulator of neuroinflammation, but whether this kinase mediates astrocytic...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401942/ https://www.ncbi.nlm.nih.gov/pubmed/37546744 http://dx.doi.org/10.1101/2023.07.21.550097 |
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author | Chang, Nydia P. DaPrano, Evan M. Evans, Wesley R. Nissenbaum, Marialaina McCourt, Micheal Alzate, Diego Lindman, Marissa Chou, Tsui-Wen Atkins, Colm Kusnecov, Alexander W. Huda, Rafiq Daniels, Brian P. |
author_facet | Chang, Nydia P. DaPrano, Evan M. Evans, Wesley R. Nissenbaum, Marialaina McCourt, Micheal Alzate, Diego Lindman, Marissa Chou, Tsui-Wen Atkins, Colm Kusnecov, Alexander W. Huda, Rafiq Daniels, Brian P. |
author_sort | Chang, Nydia P. |
collection | PubMed |
description | Astrocyte activation is a common feature of neurodegenerative diseases. However, the ways in which dying neurons influence the activity of astrocytes is poorly understood. RIPK3 signaling has recently been described as a key regulator of neuroinflammation, but whether this kinase mediates astrocytic responsiveness to neuronal death has not yet been studied. Here, we used the MPTP model of Parkinson’s disease to show that activation of astrocytic RIPK3 drives dopaminergic cell death and axon damage. Transcriptomic profiling revealed that astrocytic RIPK3 promoted gene expression associated with neuroinflammation and movement disorders, and this coincided with significant engagement of DAMP signaling. Using human cell culture systems, we show that factors released from dying neurons signal through RAGE to induce RIPK3-dependent astrocyte activation. These findings highlight a mechanism of neuron-glia crosstalk in which neuronal death perpetuates further neurodegeneration by engaging inflammatory astrocyte activation via RIPK3. |
format | Online Article Text |
id | pubmed-10401942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104019422023-08-05 Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling Chang, Nydia P. DaPrano, Evan M. Evans, Wesley R. Nissenbaum, Marialaina McCourt, Micheal Alzate, Diego Lindman, Marissa Chou, Tsui-Wen Atkins, Colm Kusnecov, Alexander W. Huda, Rafiq Daniels, Brian P. bioRxiv Article Astrocyte activation is a common feature of neurodegenerative diseases. However, the ways in which dying neurons influence the activity of astrocytes is poorly understood. RIPK3 signaling has recently been described as a key regulator of neuroinflammation, but whether this kinase mediates astrocytic responsiveness to neuronal death has not yet been studied. Here, we used the MPTP model of Parkinson’s disease to show that activation of astrocytic RIPK3 drives dopaminergic cell death and axon damage. Transcriptomic profiling revealed that astrocytic RIPK3 promoted gene expression associated with neuroinflammation and movement disorders, and this coincided with significant engagement of DAMP signaling. Using human cell culture systems, we show that factors released from dying neurons signal through RAGE to induce RIPK3-dependent astrocyte activation. These findings highlight a mechanism of neuron-glia crosstalk in which neuronal death perpetuates further neurodegeneration by engaging inflammatory astrocyte activation via RIPK3. Cold Spring Harbor Laboratory 2023-07-24 /pmc/articles/PMC10401942/ /pubmed/37546744 http://dx.doi.org/10.1101/2023.07.21.550097 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Chang, Nydia P. DaPrano, Evan M. Evans, Wesley R. Nissenbaum, Marialaina McCourt, Micheal Alzate, Diego Lindman, Marissa Chou, Tsui-Wen Atkins, Colm Kusnecov, Alexander W. Huda, Rafiq Daniels, Brian P. Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling |
title | Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling |
title_full | Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling |
title_fullStr | Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling |
title_full_unstemmed | Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling |
title_short | Neuronal DAMPs exacerbate neurodegeneration via astrocytic RIPK3 signaling |
title_sort | neuronal damps exacerbate neurodegeneration via astrocytic ripk3 signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401942/ https://www.ncbi.nlm.nih.gov/pubmed/37546744 http://dx.doi.org/10.1101/2023.07.21.550097 |
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