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Proof-of concept that an acute trophic factors intervention after spinal cord injury provides an adequate niche for neuroprotection, recruitment of nestin-expressing progenitors and regeneration

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dc.contributor.author Krityakiarana W.
dc.contributor.author Zhao P.M.
dc.contributor.author Nguyen K.
dc.contributor.author Gomez-Pinilla F.
dc.contributor.author Kotchabhakdi N.
dc.contributor.author De Vellis J.
dc.contributor.author Espinosa-Jeffrey A.
dc.date.accessioned 2021-04-05T03:24:10Z
dc.date.available 2021-04-05T03:24:10Z
dc.date.issued 2016
dc.identifier.issn 3643190
dc.identifier.other 2-s2.0-84958751578
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/13474
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958751578&doi=10.1007%2fs11064-016-1850-z&partnerID=40&md5=8d3d558d572c97d4921f430836c45792
dc.description.abstract Trophic factor treatment has been shown to improve the recovery of brain and spinal cord injury (SCI). In this study, we examined the effects of TSC1 (a combination of insulin-like growth factor 1 and transferrin) 4 and 8 h after SCI at the thoracic segment level (T12) in nestin- GFP transgenic mice. TSC1 treatment for 4 and 8 h increased the number of nestin-expressing cells around the lesion site and prevented Wallerian degeneration. Treatment with TSC1 for 4 h significantly increased heat shock protein (HSP)-32 and HSP-70 expression 1 and 2 mm from lesion site (both, caudal and rostral). Conversely, the number of HSP-32 positive cells decreased after an 8-h TSC1 treatment, although it was still higher than in both, non-treated SCI and intact spinal cord animals. Furthermore, TSC1 increased NG2 expressing cell numbers and preserved most axons intact, facilitating remyelination and repair. These results support our hypothesis that TSC1 is an effective treatment for cell and tissue neuroprotection after SCI. An early intervention is crucial to prevent secondary damage of the injured SC and, in particular, to prevent Wallerian degeneration. © Springer Science+Business Media New York 2016.
dc.subject brain derived neurotrophic factor
dc.subject epidermal growth factor receptor
dc.subject glial cell line derived neurotrophic factor
dc.subject green fluorescent protein
dc.subject heat shock protein 70
dc.subject heme oxygenase 1
dc.subject hybrid protein
dc.subject intermediate filament protein
dc.subject nestin
dc.subject recombinant growth factor
dc.subject somatomedin C
dc.subject transferrin
dc.subject TSC1
dc.subject unclassified drug
dc.subject nestin
dc.subject neuroprotective agent
dc.subject animal cell
dc.subject animal experiment
dc.subject animal model
dc.subject animal tissue
dc.subject Article
dc.subject axon
dc.subject cell count
dc.subject cell regeneration
dc.subject controlled study
dc.subject cytoarchitecture
dc.subject demyelination
dc.subject early intervention
dc.subject gray matter
dc.subject immunohistochemistry
dc.subject mitochondrion
dc.subject motoneuron
dc.subject mouse
dc.subject neural stem cell
dc.subject neuroprotection
dc.subject nonhuman
dc.subject oxidative stress
dc.subject priority journal
dc.subject protein expression
dc.subject protein phosphorylation
dc.subject remyelinization
dc.subject spinal cord
dc.subject spinal cord injury
dc.subject stem cell niche
dc.subject Wallerian degeneration
dc.subject white matter
dc.subject animal
dc.subject metabolism
dc.subject pathophysiology
dc.subject spinal cord injury
dc.subject stem cell
dc.subject transgenic mouse
dc.subject Animals
dc.subject Mice
dc.subject Mice, Transgenic
dc.subject Nestin
dc.subject Neuroprotective Agents
dc.subject Spinal Cord Injuries
dc.subject Stem Cells
dc.title Proof-of concept that an acute trophic factors intervention after spinal cord injury provides an adequate niche for neuroprotection, recruitment of nestin-expressing progenitors and regeneration
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Neurochemical Research. Vol 41, (2016), p.431-449
dc.identifier.doi 10.1007/s11064-016-1850-z


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