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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

dc.contributor.authorWarin Krityakiaranaen_US
dc.contributor.authorPaul M. Zhaoen_US
dc.contributor.authorKevin Nguyenen_US
dc.contributor.authorFernando Gomez-Pinillaen_US
dc.contributor.authorNaiphinich Kotchabhakdien_US
dc.contributor.authorJean De Vellisen_US
dc.contributor.authorAraceli Espinosa-Jeffreyen_US
dc.contributor.otherJane & Terry Semel Institute for Neuroscience & Human Behavioren_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.contributor.otherUniversity of California, Los Angelesen_US
dc.contributor.otherUniversity of Tokyoen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.date.accessioned2018-12-11T02:19:25Z
dc.date.accessioned2019-03-14T08:04:10Z
dc.date.available2018-12-11T02:19:25Z
dc.date.available2019-03-14T08:04:10Z
dc.date.issued2016-02-17en_US
dc.description.abstract© Springer Science+Business Media New York 2016. 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.en_US
dc.identifier.citationNeurochemical Research. Vol.41, No.1-2 (2016), 431-449en_US
dc.identifier.doi10.1007/s11064-016-1850-zen_US
dc.identifier.issn15736903en_US
dc.identifier.issn03643190en_US
dc.identifier.other2-s2.0-84958751578en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/43101
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84958751578&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
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 regenerationen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84958751578&origin=inwarden_US

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