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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 |
Authors: | Krityakiarana W. Zhao P.M. Nguyen K. Gomez-Pinilla F. Kotchabhakdi N. De Vellis J. Espinosa-Jeffrey A. |
Keywords: | brain derived neurotrophic factor epidermal growth factor receptor glial cell line derived neurotrophic factor green fluorescent protein heat shock protein 70 heme oxygenase 1 hybrid protein intermediate filament protein nestin recombinant growth factor somatomedin C transferrin TSC1 unclassified drug nestin neuroprotective agent animal cell animal experiment animal model animal tissue Article axon cell count cell regeneration controlled study cytoarchitecture demyelination early intervention gray matter immunohistochemistry mitochondrion motoneuron mouse neural stem cell neuroprotection nonhuman oxidative stress priority journal protein expression protein phosphorylation remyelinization spinal cord spinal cord injury stem cell niche Wallerian degeneration white matter animal metabolism pathophysiology spinal cord injury stem cell transgenic mouse Animals Mice Mice, Transgenic Nestin Neuroprotective Agents Spinal Cord Injuries Stem Cells |
Issue Date: | 2016 |
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. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13474 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958751578&doi=10.1007%2fs11064-016-1850-z&partnerID=40&md5=8d3d558d572c97d4921f430836c45792 |
ISSN: | 3643190 |
Appears in Collections: | Scopus 1983-2021 |
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