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LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting
Injury to the adult mammalian central nervous system induces compensatory plasticity of spared axons—referred to as collateral axon sprouting—that can facilitate neural recovery. The contribution of reactive astrocytes to axon sprouting remains elusive. Here, we sought to investigate the role of axo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520579/ https://www.ncbi.nlm.nih.gov/pubmed/36187291 http://dx.doi.org/10.3389/fncel.2022.969261 |
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author | Chen, Meifan Ingle, Laura Plautz, Erik J. Kong, Xiangmei Tang, Rui Ghosh, Neil Romprey, Megan K. Fenske, William K. Goldberg, Mark P. |
author_facet | Chen, Meifan Ingle, Laura Plautz, Erik J. Kong, Xiangmei Tang, Rui Ghosh, Neil Romprey, Megan K. Fenske, William K. Goldberg, Mark P. |
author_sort | Chen, Meifan |
collection | PubMed |
description | Injury to the adult mammalian central nervous system induces compensatory plasticity of spared axons—referred to as collateral axon sprouting—that can facilitate neural recovery. The contribution of reactive astrocytes to axon sprouting remains elusive. Here, we sought to investigate the role of axon degeneration-reactive astrocytes in the regulation of collateral axon sprouting that occurs in the mouse spinal cord after unilateral photothrombotic stroke of the primary motor cortex. We identified astrocytic leucine zipper-bearing kinase (LZK) as a positive regulator of astrocyte reactivity to corticospinal axon degeneration. Remarkably, genetic stimulation of astrocyte reactivity, via LZK overexpression in adult astrocytes, enhanced corticospinal axon sprouting. LZK promoted the production of astrocyte-derived ciliary neurotrophic factor (CNTF) that likely enhanced axon growth in mice with astrocytic LZK overexpression after injury. Our finding that LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting highlights the potential of engineering astrocytes to support injury-induced axon plasticity for neural repair. |
format | Online Article Text |
id | pubmed-9520579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95205792022-09-30 LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting Chen, Meifan Ingle, Laura Plautz, Erik J. Kong, Xiangmei Tang, Rui Ghosh, Neil Romprey, Megan K. Fenske, William K. Goldberg, Mark P. Front Cell Neurosci Neuroscience Injury to the adult mammalian central nervous system induces compensatory plasticity of spared axons—referred to as collateral axon sprouting—that can facilitate neural recovery. The contribution of reactive astrocytes to axon sprouting remains elusive. Here, we sought to investigate the role of axon degeneration-reactive astrocytes in the regulation of collateral axon sprouting that occurs in the mouse spinal cord after unilateral photothrombotic stroke of the primary motor cortex. We identified astrocytic leucine zipper-bearing kinase (LZK) as a positive regulator of astrocyte reactivity to corticospinal axon degeneration. Remarkably, genetic stimulation of astrocyte reactivity, via LZK overexpression in adult astrocytes, enhanced corticospinal axon sprouting. LZK promoted the production of astrocyte-derived ciliary neurotrophic factor (CNTF) that likely enhanced axon growth in mice with astrocytic LZK overexpression after injury. Our finding that LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting highlights the potential of engineering astrocytes to support injury-induced axon plasticity for neural repair. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9520579/ /pubmed/36187291 http://dx.doi.org/10.3389/fncel.2022.969261 Text en Copyright © 2022 Chen, Ingle, Plautz, Kong, Tang, Ghosh, Romprey, Fenske and Goldberg. 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 | Neuroscience Chen, Meifan Ingle, Laura Plautz, Erik J. Kong, Xiangmei Tang, Rui Ghosh, Neil Romprey, Megan K. Fenske, William K. Goldberg, Mark P. LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting |
title | LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting |
title_full | LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting |
title_fullStr | LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting |
title_full_unstemmed | LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting |
title_short | LZK-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting |
title_sort | lzk-dependent stimulation of astrocyte reactivity promotes corticospinal axon sprouting |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520579/ https://www.ncbi.nlm.nih.gov/pubmed/36187291 http://dx.doi.org/10.3389/fncel.2022.969261 |
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