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Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats

BACKGROUND: Peripheral nerve injury (PNI) is one of the most debilitating injuries, but therapies for PNI are still far from satisfactory. Pyroptosis, a recently identified form of cell death, has been demonstrated to participate in different diseases. However, the role of pyroptosis of Schwann cell...

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Autores principales: Wang, Jiayi, Lu, Shunyi, Yuan, Ya, Huang, Lei, Bian, Mengxuan, Yu, Jieqin, Zou, Jiapeng, Jiang, Libo, Meng, Dehua, Zhang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154099/
https://www.ncbi.nlm.nih.gov/pubmed/37144237
http://dx.doi.org/10.1155/2023/9721375
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author Wang, Jiayi
Lu, Shunyi
Yuan, Ya
Huang, Lei
Bian, Mengxuan
Yu, Jieqin
Zou, Jiapeng
Jiang, Libo
Meng, Dehua
Zhang, Jian
author_facet Wang, Jiayi
Lu, Shunyi
Yuan, Ya
Huang, Lei
Bian, Mengxuan
Yu, Jieqin
Zou, Jiapeng
Jiang, Libo
Meng, Dehua
Zhang, Jian
author_sort Wang, Jiayi
collection PubMed
description BACKGROUND: Peripheral nerve injury (PNI) is one of the most debilitating injuries, but therapies for PNI are still far from satisfactory. Pyroptosis, a recently identified form of cell death, has been demonstrated to participate in different diseases. However, the role of pyroptosis of Schwann cells in PNI remains unclear. METHODS: We established a rat PNI model, and western blotting, transmission electron microscopy, and immunofluorescence staining were used to confirm pyroptosis of Schwann cells in PNI in vivo. In vitro, pyroptosis of Schwann cells was induced by lipopolysaccharides (LPS)+adenosine triphosphate disodium (ATP). An irreversible inhibitor of pyroptosis, acetyl (Ac)-Tyr-Val-Ala-Asp-chloromethyl ketone (Ac-YVAD-cmk), was used to attenuate Schwann cell pyroptosis. Moreover, the influence of pyroptotic Schwann cells on the function of dorsal root ganglion neurons (DRGns) was analyzed by a coculture system. Finally, the rat PNI model was intraperitoneally treated with Ac-YVAD-cmk to observe the effect of pyroptosis on nerve regeneration and motor function. RESULTS: Schwann cell pyroptosis was notably observed in the injured sciatic nerve. LPS+ATP treatment effectively induced Schwann cell pyroptosis, which was largely attenuated by Ac-YVAD-cmk. Additionally, pyroptotic Schwann cells inhibited the function of DRGns by secreting inflammatory factors. A decrease in pyroptosis in Schwann cells promoted regeneration of the sciatic nerve and recovery of motor function in rats. CONCLUSION: Given the role of Schwann cell pyroptosis in PNI progression, inhibition of Schwann cell pyroptosis might be a potential therapeutic strategy for PNI in the future.
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spelling pubmed-101540992023-05-03 Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats Wang, Jiayi Lu, Shunyi Yuan, Ya Huang, Lei Bian, Mengxuan Yu, Jieqin Zou, Jiapeng Jiang, Libo Meng, Dehua Zhang, Jian Mediators Inflamm Research Article BACKGROUND: Peripheral nerve injury (PNI) is one of the most debilitating injuries, but therapies for PNI are still far from satisfactory. Pyroptosis, a recently identified form of cell death, has been demonstrated to participate in different diseases. However, the role of pyroptosis of Schwann cells in PNI remains unclear. METHODS: We established a rat PNI model, and western blotting, transmission electron microscopy, and immunofluorescence staining were used to confirm pyroptosis of Schwann cells in PNI in vivo. In vitro, pyroptosis of Schwann cells was induced by lipopolysaccharides (LPS)+adenosine triphosphate disodium (ATP). An irreversible inhibitor of pyroptosis, acetyl (Ac)-Tyr-Val-Ala-Asp-chloromethyl ketone (Ac-YVAD-cmk), was used to attenuate Schwann cell pyroptosis. Moreover, the influence of pyroptotic Schwann cells on the function of dorsal root ganglion neurons (DRGns) was analyzed by a coculture system. Finally, the rat PNI model was intraperitoneally treated with Ac-YVAD-cmk to observe the effect of pyroptosis on nerve regeneration and motor function. RESULTS: Schwann cell pyroptosis was notably observed in the injured sciatic nerve. LPS+ATP treatment effectively induced Schwann cell pyroptosis, which was largely attenuated by Ac-YVAD-cmk. Additionally, pyroptotic Schwann cells inhibited the function of DRGns by secreting inflammatory factors. A decrease in pyroptosis in Schwann cells promoted regeneration of the sciatic nerve and recovery of motor function in rats. CONCLUSION: Given the role of Schwann cell pyroptosis in PNI progression, inhibition of Schwann cell pyroptosis might be a potential therapeutic strategy for PNI in the future. Hindawi 2023-04-25 /pmc/articles/PMC10154099/ /pubmed/37144237 http://dx.doi.org/10.1155/2023/9721375 Text en Copyright © 2023 Jiayi Wang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Jiayi
Lu, Shunyi
Yuan, Ya
Huang, Lei
Bian, Mengxuan
Yu, Jieqin
Zou, Jiapeng
Jiang, Libo
Meng, Dehua
Zhang, Jian
Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats
title Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats
title_full Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats
title_fullStr Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats
title_full_unstemmed Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats
title_short Inhibition of Schwann Cell Pyroptosis Promotes Nerve Regeneration in Peripheral Nerve Injury in Rats
title_sort inhibition of schwann cell pyroptosis promotes nerve regeneration in peripheral nerve injury in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154099/
https://www.ncbi.nlm.nih.gov/pubmed/37144237
http://dx.doi.org/10.1155/2023/9721375
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