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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
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.
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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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