Long-term cognitive deficits after traumatic brain injury associated with microglia activation

dc.contributor.authorSaba, Esber S.
dc.contributor.authorKarout, Mona
dc.contributor.authorNasralla, Leila
dc.contributor.authorKobeissy, Firas H.
dc.contributor.authorDarwish, Hala
dc.contributor.authorKhoury, Samia J.
dc.contributor.departmentExperimental Pathology, Microbiology, and Immunology
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.departmentNeurology
dc.contributor.departmentHSON
dc.contributor.departmentNehme and Therese Tohme Multiple Sclerosis (MS) Center
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.facultyRafic Hariri School of Nursing (HSON)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:39:09Z
dc.date.available2025-01-24T11:39:09Z
dc.date.issued2021
dc.description.abstractTraumatic Brain Injury (TBI) is the most prevalent of all head injuries. Microglia play an essential role in homeostasis and diseases of the central nervous system. We hypothesize that microglia may play a beneficial or detrimental role in TBI depending on their state of activation and duration. In this study, we evaluated whether TBI results in a spatiotemporal change in microglia phenotype and whether it affects sensory-motor or learning and memory functions in male C57BL/6 mice. We used a panel of neurological and behavioral tests and a multi-color flow cytometry-based data analysis followed by unsupervised clustering to evaluate isolated microglia from injured brain tissue. We characterized several microglial phenotypes and their association with cognitive deficits. TBI results in a spatiotemporal increase in activated microglia that correlated negatively with spatial learning and memory at 35 days post-injury. These observations could define therapeutic windows and accelerate translational research to improve patient outcomes. © 2021
dc.identifier.doihttps://doi.org/10.1016/j.clim.2021.108815
dc.identifier.eid2-s2.0-85111581370
dc.identifier.pmid34339843
dc.identifier.urihttp://hdl.handle.net/10938/29191
dc.language.isoen
dc.publisherAcademic Press Inc.
dc.relation.ispartofClinical Immunology
dc.sourceScopus
dc.subjectChronic inflammation
dc.subjectCognition
dc.subjectInfiltrating macrophages
dc.subjectMicroglia
dc.subjectSpatial memory
dc.subjectTraumatic brain injury
dc.subjectAnimals
dc.subjectBrain
dc.subjectBrain injuries, traumatic
dc.subjectCognitive dysfunction
dc.subjectDisease models, animal
dc.subjectFlow cytometry
dc.subjectMale
dc.subjectMaze learning
dc.subjectMice
dc.subjectMice, inbred c57bl
dc.subjectModels, neurological
dc.subjectModels, psychological
dc.subjectNonlinear dynamics
dc.subjectSpatial learning
dc.subjectSpatio-temporal analysis
dc.subjectTranslational medical research
dc.subjectAnimal
dc.subjectBiological model
dc.subjectC57bl mouse
dc.subjectClassification
dc.subjectCognitive defect
dc.subjectComplication
dc.subjectDisease model
dc.subjectMaze test
dc.subjectMouse
dc.subjectNonlinear system
dc.subjectPathology
dc.subjectPathophysiology
dc.subjectPhysiology
dc.subjectPsychological model
dc.subjectPsychology
dc.subjectSpatiotemporal analysis
dc.subjectTranslational research
dc.titleLong-term cognitive deficits after traumatic brain injury associated with microglia activation
dc.typeArticle

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