Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation

Abstract Background Inflammation-sensitized hypoxic-ischemic brain injury significantly contributes to neonatal mortality as affected neonates do not benefit from standard cooling treatments. To get further insight into inflammatory responses involved, we experimentally investigated the immune respo...

Full description

Saved in:
Bibliographic Details
Main Authors: Anna-Sophie Bremer, Nico Henschel, Hannah Burkard, Maria Eugenia Bernis, Thomas Ulas, Hemmen Sabir
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Journal of Neuroinflammation
Subjects:
Online Access:https://doi.org/10.1186/s12974-025-03516-1
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849234585682968576
author Anna-Sophie Bremer
Nico Henschel
Hannah Burkard
Maria Eugenia Bernis
Thomas Ulas
Hemmen Sabir
author_facet Anna-Sophie Bremer
Nico Henschel
Hannah Burkard
Maria Eugenia Bernis
Thomas Ulas
Hemmen Sabir
author_sort Anna-Sophie Bremer
collection DOAJ
description Abstract Background Inflammation-sensitized hypoxic-ischemic brain injury significantly contributes to neonatal mortality as affected neonates do not benefit from standard cooling treatments. To get further insight into inflammatory responses involved, we experimentally investigated the immune response of microglia in an inflammation-sensitized neonatal hypoxia-ischemia (HI) model. Results Transcriptomic analysis of microglia isolated from brains following inflammation-sensitized HI brain injury revealed a strong upregulation of leukocyte recruitment and pro-inflammatory markers. Specifically, markers associated with neutrophil-mediated immune responses and chemotaxis were upregulated in the inflammation-sensitized HI group compared to the non-inflammation-sensitized HI and control groups. Serpine 1 and Selp could be identified as specifically upregulated markers indicating an acute inflammatory condition before HI injury. Conclusion Our study revealed preliminary data about a microglia population which is primed to recruit peripheral neutrophils to infiltrate the brain and mediate neutrophil immune response. We showed a contribution to neutrophil activation in case of inflammation following HI in the brain. Targeting microglia-mediated neutrophil recruitment can indicate a possible treatment approach in case of inflammation-sensitized HI brain injury.
format Article
id doaj-art-fcee4e7a6792443088d124a8ce3ea044
institution Kabale University
issn 1742-2094
language English
publishDate 2025-07-01
publisher BMC
record_format Article
series Journal of Neuroinflammation
spelling doaj-art-fcee4e7a6792443088d124a8ce3ea0442025-08-20T04:03:06ZengBMCJournal of Neuroinflammation1742-20942025-07-0122111310.1186/s12974-025-03516-1Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activationAnna-Sophie Bremer0Nico Henschel1Hannah Burkard2Maria Eugenia Bernis3Thomas Ulas4Hemmen Sabir5Department of Neonatology and Pediatric Intensive Care, Children’s Hospital, University of BonnGerman Center for Neurodegenerative Disease (DZNE)Department of Neonatology and Pediatric Intensive Care, Children’s Hospital, University of BonnDepartment of Neonatology and Pediatric Intensive Care, Children’s Hospital, University of BonnGerman Center for Neurodegenerative Disease (DZNE)Department of Neonatology and Pediatric Intensive Care, Children’s Hospital, University of BonnAbstract Background Inflammation-sensitized hypoxic-ischemic brain injury significantly contributes to neonatal mortality as affected neonates do not benefit from standard cooling treatments. To get further insight into inflammatory responses involved, we experimentally investigated the immune response of microglia in an inflammation-sensitized neonatal hypoxia-ischemia (HI) model. Results Transcriptomic analysis of microglia isolated from brains following inflammation-sensitized HI brain injury revealed a strong upregulation of leukocyte recruitment and pro-inflammatory markers. Specifically, markers associated with neutrophil-mediated immune responses and chemotaxis were upregulated in the inflammation-sensitized HI group compared to the non-inflammation-sensitized HI and control groups. Serpine 1 and Selp could be identified as specifically upregulated markers indicating an acute inflammatory condition before HI injury. Conclusion Our study revealed preliminary data about a microglia population which is primed to recruit peripheral neutrophils to infiltrate the brain and mediate neutrophil immune response. We showed a contribution to neutrophil activation in case of inflammation following HI in the brain. Targeting microglia-mediated neutrophil recruitment can indicate a possible treatment approach in case of inflammation-sensitized HI brain injury.https://doi.org/10.1186/s12974-025-03516-1Neonatal Hypoxia-IschemiaBrain inflammationMicroglia primingNeutrophil recruitmentTranscriptomic analysis
spellingShingle Anna-Sophie Bremer
Nico Henschel
Hannah Burkard
Maria Eugenia Bernis
Thomas Ulas
Hemmen Sabir
Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation
Journal of Neuroinflammation
Neonatal Hypoxia-Ischemia
Brain inflammation
Microglia priming
Neutrophil recruitment
Transcriptomic analysis
title Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation
title_full Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation
title_fullStr Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation
title_full_unstemmed Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation
title_short Transcriptomic profile of microglia following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation
title_sort transcriptomic profile of microglia following inflammation sensitized hypoxic ischemic brain injury in neonatal rats suggests strong contribution to neutrophil chemotaxis and activation
topic Neonatal Hypoxia-Ischemia
Brain inflammation
Microglia priming
Neutrophil recruitment
Transcriptomic analysis
url https://doi.org/10.1186/s12974-025-03516-1
work_keys_str_mv AT annasophiebremer transcriptomicprofileofmicrogliafollowinginflammationsensitizedhypoxicischemicbraininjuryinneonatalratssuggestsstrongcontributiontoneutrophilchemotaxisandactivation
AT nicohenschel transcriptomicprofileofmicrogliafollowinginflammationsensitizedhypoxicischemicbraininjuryinneonatalratssuggestsstrongcontributiontoneutrophilchemotaxisandactivation
AT hannahburkard transcriptomicprofileofmicrogliafollowinginflammationsensitizedhypoxicischemicbraininjuryinneonatalratssuggestsstrongcontributiontoneutrophilchemotaxisandactivation
AT mariaeugeniabernis transcriptomicprofileofmicrogliafollowinginflammationsensitizedhypoxicischemicbraininjuryinneonatalratssuggestsstrongcontributiontoneutrophilchemotaxisandactivation
AT thomasulas transcriptomicprofileofmicrogliafollowinginflammationsensitizedhypoxicischemicbraininjuryinneonatalratssuggestsstrongcontributiontoneutrophilchemotaxisandactivation
AT hemmensabir transcriptomicprofileofmicrogliafollowinginflammationsensitizedhypoxicischemicbraininjuryinneonatalratssuggestsstrongcontributiontoneutrophilchemotaxisandactivation