Publication:
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.contributor.authorKrityakiarana W.
dc.contributor.authorZhao P.M.
dc.contributor.authorNguyen K.
dc.contributor.authorGomez-Pinilla F.
dc.contributor.authorKotchabhakdi N.
dc.contributor.authorDe Vellis J.
dc.contributor.authorEspinosa-Jeffrey A.
dc.date.accessioned2021-04-05T03:24:10Z
dc.date.available2021-04-05T03:24:10Z
dc.date.issued2016
dc.date.issuedBE2559
dc.description.abstractTrophic 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.format.mimetypeapplication/pdf
dc.identifier.citationNeurochemical Research. Vol 41, (2016), p.431-449
dc.identifier.doi10.1007/s11064-016-1850-z
dc.identifier.issn3643190
dc.identifier.other2-s2.0-84958751578
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5639
dc.rights.holderScopus
dc.subject.otherBrain derived neurotrophic factor
dc.subject.otherEpidermal growth factor receptor
dc.subject.otherGlial cell line derived neurotrophic factor
dc.subject.otherGreen fluorescent protein
dc.subject.otherHeat shock protein 70
dc.subject.otherHeme oxygenase 1
dc.subject.otherHybrid protein
dc.subject.otherIntermediate filament protein
dc.subject.otherNestin
dc.subject.otherRecombinant growth factor
dc.subject.otherSomatomedin C
dc.subject.otherTransferrin
dc.subject.otherTSC1
dc.subject.otherUnclassified drug
dc.subject.otherNestin
dc.subject.otherNeuroprotective agent
dc.subject.otherAnimal cell
dc.subject.otherAnimal experiment
dc.subject.otherAnimal model
dc.subject.otherAnimal tissue
dc.subject.otherArticle
dc.subject.otherAxon
dc.subject.otherCell count
dc.subject.otherCell regeneration
dc.subject.otherControlled study
dc.subject.otherCytoarchitecture
dc.subject.otherDemyelination
dc.subject.otherEarly intervention
dc.subject.otherGray matter
dc.subject.otherImmunohistochemistry
dc.subject.otherMitochondrion
dc.subject.otherMotoneuron
dc.subject.otherMouse
dc.subject.otherNeural stem cell
dc.subject.otherNeuroprotection
dc.subject.otherNonhuman
dc.subject.otherOxidative stress
dc.subject.otherPriority journal
dc.subject.otherProtein expression
dc.subject.otherProtein phosphorylation
dc.subject.otherRemyelinization
dc.subject.otherSpinal cord
dc.subject.otherSpinal cord injury
dc.subject.otherStem cell niche
dc.subject.otherWallerian degeneration
dc.subject.otherWhite matter
dc.subject.otherAnimal
dc.subject.otherMetabolism
dc.subject.otherPathophysiology
dc.subject.otherSpinal cord injury
dc.subject.otherStem cell
dc.subject.otherTransgenic mouse
dc.subject.otherAnimals
dc.subject.otherMice
dc.subject.otherMice, Transgenic
dc.subject.otherNestin
dc.subject.otherNeuroprotective Agents
dc.subject.otherSpinal Cord Injuries
dc.subject.otherStem Cells
dc.titleProof-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.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84958751578&doi=10.1007%2fs11064-016-1850-z&partnerID=40&md5=8d3d558d572c97d4921f430836c45792

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