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Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury
AIMS: To investigate astrocyte‐related phagocytosis of synapses in the ipsilateral hippocampus after traumatic brain injury (TBI). METHODS: We performed controlled cortical impact to simulate TBI in mice. Seven days postinjury, we performed cognitive tests, synapse quantification, and examination of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493650/ https://www.ncbi.nlm.nih.gov/pubmed/37081759 http://dx.doi.org/10.1111/cns.14223 |
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author | Zhuang, Yuan Xu, Xiaojian Li, Hao Niu, Fei Yang, Mengshi Ge, Qianqian Lu, Shenghua Deng, Yu Wu, Hongbin Zhang, Bin Liu, Baiyun |
author_facet | Zhuang, Yuan Xu, Xiaojian Li, Hao Niu, Fei Yang, Mengshi Ge, Qianqian Lu, Shenghua Deng, Yu Wu, Hongbin Zhang, Bin Liu, Baiyun |
author_sort | Zhuang, Yuan |
collection | PubMed |
description | AIMS: To investigate astrocyte‐related phagocytosis of synapses in the ipsilateral hippocampus after traumatic brain injury (TBI). METHODS: We performed controlled cortical impact to simulate TBI in mice. Seven days postinjury, we performed cognitive tests, synapse quantification, and examination of astrocytic phagocytosis in association with Megf10 expression. RESULTS: During the subacute stage post‐TBI, we found a reduction in excitatory postsynaptic materials in the ipsilateral hippocampus, which was consistent with poor performance in the cognitive test. The transcriptome data suggested that robust phagocytosis was responsible for this process. Coincidently, we identified phagocytic astrocytes containing secondary lysosomes that were wrapped around the synapses in the ipsilateral hippocampus. Moreover, a significant increase in the co‐location of GFAP and PSD‐95 in the CA1 region suggested astrocytic engulfment of excitatory postsynaptic proteins. After examining the reported phagocytic pathways, we found that both the transcription level and protein expression of Megf10 were elevated. Co‐immunofluorescence of GFAP and Megf10 demonstrated that the expression of Megf10 was spatially upregulated in astrocytes, exclusively in the CA1 region, and was related to the astrocytic engulfment of PSD‐95. CONCLUSION: Our study elaborated that the Megf10‐related astrocytic engulfment of PSD‐95 in the CA1 region of the ipsilateral hippocampus aggravated cognitive dysfunction following severe TBI. |
format | Online Article Text |
id | pubmed-10493650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104936502023-09-12 Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury Zhuang, Yuan Xu, Xiaojian Li, Hao Niu, Fei Yang, Mengshi Ge, Qianqian Lu, Shenghua Deng, Yu Wu, Hongbin Zhang, Bin Liu, Baiyun CNS Neurosci Ther Original Articles AIMS: To investigate astrocyte‐related phagocytosis of synapses in the ipsilateral hippocampus after traumatic brain injury (TBI). METHODS: We performed controlled cortical impact to simulate TBI in mice. Seven days postinjury, we performed cognitive tests, synapse quantification, and examination of astrocytic phagocytosis in association with Megf10 expression. RESULTS: During the subacute stage post‐TBI, we found a reduction in excitatory postsynaptic materials in the ipsilateral hippocampus, which was consistent with poor performance in the cognitive test. The transcriptome data suggested that robust phagocytosis was responsible for this process. Coincidently, we identified phagocytic astrocytes containing secondary lysosomes that were wrapped around the synapses in the ipsilateral hippocampus. Moreover, a significant increase in the co‐location of GFAP and PSD‐95 in the CA1 region suggested astrocytic engulfment of excitatory postsynaptic proteins. After examining the reported phagocytic pathways, we found that both the transcription level and protein expression of Megf10 were elevated. Co‐immunofluorescence of GFAP and Megf10 demonstrated that the expression of Megf10 was spatially upregulated in astrocytes, exclusively in the CA1 region, and was related to the astrocytic engulfment of PSD‐95. CONCLUSION: Our study elaborated that the Megf10‐related astrocytic engulfment of PSD‐95 in the CA1 region of the ipsilateral hippocampus aggravated cognitive dysfunction following severe TBI. John Wiley and Sons Inc. 2023-04-20 /pmc/articles/PMC10493650/ /pubmed/37081759 http://dx.doi.org/10.1111/cns.14223 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Zhuang, Yuan Xu, Xiaojian Li, Hao Niu, Fei Yang, Mengshi Ge, Qianqian Lu, Shenghua Deng, Yu Wu, Hongbin Zhang, Bin Liu, Baiyun Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury |
title | Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury |
title_full | Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury |
title_fullStr | Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury |
title_full_unstemmed | Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury |
title_short | Megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury |
title_sort | megf10‐related engulfment of excitatory postsynapses by astrocytes following severe brain injury |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493650/ https://www.ncbi.nlm.nih.gov/pubmed/37081759 http://dx.doi.org/10.1111/cns.14223 |
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