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Extracellular vesicles released after cranial radiation: An insight into an early mechanism of brain injury

Cranial radiation is important for treating both primary brain tumors and brain metastases. A potential delayed side effect of cranial radiation is neurocognitive function decline. Early detection of CNS injury might prevent further neuronal damage. Extracellular vesicles (EVs) have emerged as a pot...

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Detalles Bibliográficos
Autores principales: Sukati, Suriyan, Ho, Jenni, Chaiswing, Luksana, Sompol, Pradoldej, Pandit, Harshul, Wei, Wendy, Izumi, Tadahide, Chen, Quan, Weiss, Heidi, Noel, Teresa, Bondada, Subbarao, Allan Butterfield, D., St. Clair, Daret K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918058/
https://www.ncbi.nlm.nih.gov/pubmed/35183524
http://dx.doi.org/10.1016/j.brainres.2022.147840
Descripción
Sumario:Cranial radiation is important for treating both primary brain tumors and brain metastases. A potential delayed side effect of cranial radiation is neurocognitive function decline. Early detection of CNS injury might prevent further neuronal damage. Extracellular vesicles (EVs) have emerged as a potential diagnostic tool because of their unique membranous characteristics and cargos. We investigated whether EVs can be an early indicator of CNS injury by giving C57BJ/6 mice 10 Gy cranial IR. EVs were isolated from sera to quantify: 1) number of EVs using nanoparticle tracking analysis (NTA); 2) Glial fibrillary acidic protein (GFAP), an astrocyte marker; and 3) protein-bound 4-hydroxy-2-nonenal (HNE) adducts, an oxidative damage marker. Brain tissues were prepared for immunohistochemistry staining and protein immunoblotting. The results demonstrate: 1) increased GFAP levels (p < 0.05) in EVs, but not brain tissue, in the IR group; and 2) increased HNE-bound protein adduction levels (p < 0.05). The results support using EVs as an early indicator of cancer therapy-induced neuronal injury.