Sex-dependent temporal changes in astrocyte-vessel interactions following diffuse traumatic brain injury in rats.

aging with TBI blood-brain barrier cerebrovascular astrocytes chronic neurodegeneration diffuse axonal injury glial fibrillary acidic protein perivascular astrocytes

Journal

Frontiers in physiology
ISSN: 1664-042X
Titre abrégé: Front Physiol
Pays: Switzerland
ID NLM: 101549006

Informations de publication

Date de publication:
2024
Historique:
received: 23 07 2024
accepted: 11 09 2024
medline: 10 10 2024
pubmed: 10 10 2024
entrez: 10 10 2024
Statut: epublish

Résumé

Traumatic brain injury (TBI) is associated with diffuse axonal injury (DAI), a primary pathology linked to progressive neurodegeneration and neuroinflammation, including chronic astrogliosis, which influences long-term post-TBI recovery and morbidity. Sex-based differences in blood-brain barrier (BBB) permeability increases the risk of accelerated brain aging and early-onset neurodegeneration. However, few studies have evaluated chronic time course of astrocytic responses around cerebrovascular in the context of aging after TBI and sex dependence. We observed increased glial fibrillary acidic protein (GFAP)-labeled accessory processes branching near and connecting with GFAP-ensheathed cortical vessels, suggesting a critical nuance in astrocyte-vessel interactions after TBI. To quantify this observation, male and female Sprague Dawley rats (∼3 months old, n = 5-6/group) underwent either sham surgery or midline fluid percussion injury. Using immunohistochemical analysis, we quantified GFAP-labeled astrocyte primary and accessory processes that contacted GFAP-ensheathed vessels in the somatosensory barrel cortex at 7, 56, and 168 days post-injury (DPI). TBI significantly increased GFAP-positive primary processes at 7 DPI (

Identifiants

pubmed: 39387100
doi: 10.3389/fphys.2024.1469073
pii: 1469073
pmc: PMC11461938
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1469073

Informations de copyright

Copyright © 2024 Sabetta, Krishna, Curry-Koski, Lopez, Adelson and Thomas.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Zackary Sabetta (Z)

Department of Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, United States.
A.T. Still University Kirksville College of Osteopathic Medicine, Kirksville, MO, United States.

Gokul Krishna (G)

Department of Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, United States.
Translational Neurotrauma and Neurochemistry, Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, United States.

Tala Curry-Koski (T)

Department of Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, United States.
Translational Neurotrauma and Neurochemistry, Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, United States.

Mackenzie Lopez (M)

Department of Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, United States.

P David Adelson (PD)

West Virginia University School of Medicine, Rockefeller Neuroscience Institute, Morgantown, WV, United States.

Theresa Currier Thomas (TC)

Department of Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, United States.
Translational Neurotrauma and Neurochemistry, Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, AZ, United States.
Phoenix VA Healthcare System, Phoenix, AZ, United States.

Classifications MeSH