Time-dependent cytokine and chemokine changes in mouse cerebral cortex following a mild traumatic brain injury

Autor: Nigel H. Greig, Barry J. Hoffer, Edward J. Goetzl, Chaim G. Pick, Hanuma Kumar Karnati, David Tweedie, Roger J. Mullins, Dimitrios Kapogiannis
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
Chemokine
Pathology
Vascular Endothelial Growth Factor B
Mouse
medicine.medical_treatment
Cell Cycle Proteins
Mice
0302 clinical medicine
Immunology and Inflammation
Gene Regulatory Networks
Biology (General)
Cerebral Cortex
biology
General Neuroscience
Head injury
General Medicine
Extracellular vesicle
Cytokine
Cytokines
Medicine
medicine.symptom
Chemokines
protein marker
Research Article
medicine.medical_specialty
Traumatic brain injury
QH301-705.5
Science
Inflammation
GPI-Linked Proteins
General Biochemistry
Genetics and Molecular Biology

03 medical and health sciences
Extracellular Vesicles
mild traumatic brain injury
medicine
Animals
Pathological
CXCL16
Brain Concussion
General Immunology and Microbiology
business.industry
Chemokine CXCL16
medicine.disease
Disease Models
Animal

030104 developmental biology
Gene Ontology
inflammation
Brain Injuries
biology.protein
business
Transcriptome
030217 neurology & neurosurgery
Biomarkers
Neuroscience
Zdroj: eLife, Vol 9 (2020)
eLife
Popis: Traumatic brain injury (TBI) is a serious global health problem, many individuals live with TBI-related neurological dysfunction. A lack of biomarkers of TBI has impeded medication development. To identify new potential biomarkers, we time-dependently evaluated mouse brain tissue and neuronally derived plasma extracellular vesicle proteins in a mild model of TBI with parallels to concussive head injury. Mice (CD-1, 30–40 g) received a sham procedure or 30 g weight-drop and were euthanized 8, 24, 48, 72, 96 hr, 7, 14 and 30 days later. We quantified ipsilateral cortical proteins, many of which differed from sham by 8 hours post-mTBI, particularly GAS-1 and VEGF-B were increased while CXCL16 reduced, 23 proteins changed in 4 or more of the time points. Gene ontology pathways mapped from altered proteins over time related to pathological and physiological processes. Validation of proteins identified in this study may provide utility as treatment response biomarkers.
Databáze: OpenAIRE