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Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy
Sepsis-associated encephalopathy (SAE) is a severe and frequent complication of sepsis causing delirium, coma, and long-term cognitive dysfunction. We identified microglia and C1q complement activation in hippocampal autopsy tissue of patients with sepsis and increased C1q-mediated synaptic pruning...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219600/ https://www.ncbi.nlm.nih.gov/pubmed/37235660 http://dx.doi.org/10.1126/sciadv.abq7806 |
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author | Chung, Ha-Yeun Wickel, Jonathan Hahn, Nina Mein, Nils Schwarzbrunn, Meike Koch, Philipp Ceanga, Mihai Haselmann, Holger Baade-Büttner, Carolin von Stackelberg, Nikolai Hempel, Nina Schmidl, Lars Groth, Marco Andreas, Nico Götze, Juliane Coldewey, Sina M. Bauer, Michael Mawrin, Christian Dargvainiene, Justina Leypoldt, Frank Steinke, Stephan Wang, Zhao-Qi Hust, Michael Geis, Christian |
author_facet | Chung, Ha-Yeun Wickel, Jonathan Hahn, Nina Mein, Nils Schwarzbrunn, Meike Koch, Philipp Ceanga, Mihai Haselmann, Holger Baade-Büttner, Carolin von Stackelberg, Nikolai Hempel, Nina Schmidl, Lars Groth, Marco Andreas, Nico Götze, Juliane Coldewey, Sina M. Bauer, Michael Mawrin, Christian Dargvainiene, Justina Leypoldt, Frank Steinke, Stephan Wang, Zhao-Qi Hust, Michael Geis, Christian |
author_sort | Chung, Ha-Yeun |
collection | PubMed |
description | Sepsis-associated encephalopathy (SAE) is a severe and frequent complication of sepsis causing delirium, coma, and long-term cognitive dysfunction. We identified microglia and C1q complement activation in hippocampal autopsy tissue of patients with sepsis and increased C1q-mediated synaptic pruning in a murine polymicrobial sepsis model. Unbiased transcriptomics of hippocampal tissue and isolated microglia derived from septic mice revealed an involvement of the innate immune system, complement activation, and up-regulation of lysosomal pathways during SAE in parallel to neuronal and synaptic damage. Microglial engulfment of C1q-tagged synapses could be prevented by stereotactic intrahippocampal injection of a specific C1q-blocking antibody. Pharmacologically targeting microglia by PLX5622, a CSF1-R inhibitor, reduced C1q levels and the number of C1q-tagged synapses, protected from neuronal damage and synapse loss, and improved neurocognitive outcome. Thus, we identified complement-dependent synaptic pruning by microglia as a crucial pathomechanism for the development of neuronal defects during SAE. |
format | Online Article Text |
id | pubmed-10219600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-102196002023-05-27 Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy Chung, Ha-Yeun Wickel, Jonathan Hahn, Nina Mein, Nils Schwarzbrunn, Meike Koch, Philipp Ceanga, Mihai Haselmann, Holger Baade-Büttner, Carolin von Stackelberg, Nikolai Hempel, Nina Schmidl, Lars Groth, Marco Andreas, Nico Götze, Juliane Coldewey, Sina M. Bauer, Michael Mawrin, Christian Dargvainiene, Justina Leypoldt, Frank Steinke, Stephan Wang, Zhao-Qi Hust, Michael Geis, Christian Sci Adv Neuroscience Sepsis-associated encephalopathy (SAE) is a severe and frequent complication of sepsis causing delirium, coma, and long-term cognitive dysfunction. We identified microglia and C1q complement activation in hippocampal autopsy tissue of patients with sepsis and increased C1q-mediated synaptic pruning in a murine polymicrobial sepsis model. Unbiased transcriptomics of hippocampal tissue and isolated microglia derived from septic mice revealed an involvement of the innate immune system, complement activation, and up-regulation of lysosomal pathways during SAE in parallel to neuronal and synaptic damage. Microglial engulfment of C1q-tagged synapses could be prevented by stereotactic intrahippocampal injection of a specific C1q-blocking antibody. Pharmacologically targeting microglia by PLX5622, a CSF1-R inhibitor, reduced C1q levels and the number of C1q-tagged synapses, protected from neuronal damage and synapse loss, and improved neurocognitive outcome. Thus, we identified complement-dependent synaptic pruning by microglia as a crucial pathomechanism for the development of neuronal defects during SAE. American Association for the Advancement of Science 2023-05-26 /pmc/articles/PMC10219600/ /pubmed/37235660 http://dx.doi.org/10.1126/sciadv.abq7806 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience Chung, Ha-Yeun Wickel, Jonathan Hahn, Nina Mein, Nils Schwarzbrunn, Meike Koch, Philipp Ceanga, Mihai Haselmann, Holger Baade-Büttner, Carolin von Stackelberg, Nikolai Hempel, Nina Schmidl, Lars Groth, Marco Andreas, Nico Götze, Juliane Coldewey, Sina M. Bauer, Michael Mawrin, Christian Dargvainiene, Justina Leypoldt, Frank Steinke, Stephan Wang, Zhao-Qi Hust, Michael Geis, Christian Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy |
title | Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy |
title_full | Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy |
title_fullStr | Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy |
title_full_unstemmed | Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy |
title_short | Microglia mediate neurocognitive deficits by eliminating C1q-tagged synapses in sepsis-associated encephalopathy |
title_sort | microglia mediate neurocognitive deficits by eliminating c1q-tagged synapses in sepsis-associated encephalopathy |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219600/ https://www.ncbi.nlm.nih.gov/pubmed/37235660 http://dx.doi.org/10.1126/sciadv.abq7806 |
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