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Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission

Glia-mediated inflammatory processes are crucial in the pathogenesis of Parkinson’s disease (PD). As the most abundant cells of the brain and active participants in neuroinflammatory responses, astrocytes largely propagate inflammatory signals and amplify neuronal loss. Hence, intensive control of a...

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Autores principales: Song, Nanshan, Zhu, Hong, Xu, Rong, Liu, Jiaqi, Fang, Yinquan, Zhang, Jing, Ding, Jianhua, Hu, Gang, Lu, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876245/
https://www.ncbi.nlm.nih.gov/pubmed/33584303
http://dx.doi.org/10.3389/fphar.2020.618992
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author Song, Nanshan
Zhu, Hong
Xu, Rong
Liu, Jiaqi
Fang, Yinquan
Zhang, Jing
Ding, Jianhua
Hu, Gang
Lu, Ming
author_facet Song, Nanshan
Zhu, Hong
Xu, Rong
Liu, Jiaqi
Fang, Yinquan
Zhang, Jing
Ding, Jianhua
Hu, Gang
Lu, Ming
author_sort Song, Nanshan
collection PubMed
description Glia-mediated inflammatory processes are crucial in the pathogenesis of Parkinson’s disease (PD). As the most abundant cells of the brain and active participants in neuroinflammatory responses, astrocytes largely propagate inflammatory signals and amplify neuronal loss. Hence, intensive control of astrocytic activation is necessary to prevent neurodegeneration. In this study, we report that the astrocytic kir6.2, as a abnormal response after inflammatory stimuli, promotes the reactivity of A1 neurotoxic astrocytes. Using kir6.2 knockout (KO) mice, we find reversal effects of kir6.2 deficiency on A1-like astrocyte activation and death of dopaminergic neurons in lipopolysaccharide (LPS)-induced mouse models for PD. Further in vitro experiments show that aberrant kir6.2 expression induced by inflammatory irritants in astrocytes mediates the dynamin-related protein 1 (Drp1)-dependent excessive mitochondrial fragmentation and results in mitochondrial malfunctions. By deleting kir6.2, astrocytic activation is reduced and astrocytes-derived neuronal injury is prevented. We therefore conclude that astrocytic kir6.2 can potentially elucidate the pathology of PD and promote the development of therapeutic strategies for PD.
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spelling pubmed-78762452021-02-12 Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission Song, Nanshan Zhu, Hong Xu, Rong Liu, Jiaqi Fang, Yinquan Zhang, Jing Ding, Jianhua Hu, Gang Lu, Ming Front Pharmacol Pharmacology Glia-mediated inflammatory processes are crucial in the pathogenesis of Parkinson’s disease (PD). As the most abundant cells of the brain and active participants in neuroinflammatory responses, astrocytes largely propagate inflammatory signals and amplify neuronal loss. Hence, intensive control of astrocytic activation is necessary to prevent neurodegeneration. In this study, we report that the astrocytic kir6.2, as a abnormal response after inflammatory stimuli, promotes the reactivity of A1 neurotoxic astrocytes. Using kir6.2 knockout (KO) mice, we find reversal effects of kir6.2 deficiency on A1-like astrocyte activation and death of dopaminergic neurons in lipopolysaccharide (LPS)-induced mouse models for PD. Further in vitro experiments show that aberrant kir6.2 expression induced by inflammatory irritants in astrocytes mediates the dynamin-related protein 1 (Drp1)-dependent excessive mitochondrial fragmentation and results in mitochondrial malfunctions. By deleting kir6.2, astrocytic activation is reduced and astrocytes-derived neuronal injury is prevented. We therefore conclude that astrocytic kir6.2 can potentially elucidate the pathology of PD and promote the development of therapeutic strategies for PD. Frontiers Media S.A. 2021-01-28 /pmc/articles/PMC7876245/ /pubmed/33584303 http://dx.doi.org/10.3389/fphar.2020.618992 Text en Copyright © 2021 Song, Zhu, Xu, Liu, Fang, Zhang, Ding, Hu and Lu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Song, Nanshan
Zhu, Hong
Xu, Rong
Liu, Jiaqi
Fang, Yinquan
Zhang, Jing
Ding, Jianhua
Hu, Gang
Lu, Ming
Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission
title Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission
title_full Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission
title_fullStr Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission
title_full_unstemmed Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission
title_short Induced Expression of kir6.2 in A1 Astrocytes Propagates Inflammatory Neurodegeneration via Drp1-dependent Mitochondrial Fission
title_sort induced expression of kir6.2 in a1 astrocytes propagates inflammatory neurodegeneration via drp1-dependent mitochondrial fission
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876245/
https://www.ncbi.nlm.nih.gov/pubmed/33584303
http://dx.doi.org/10.3389/fphar.2020.618992
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