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
© 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 s...
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th-mahidol.431012019-03-14T15:04:10Z 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 Warin Krityakiarana Paul M. Zhao Kevin Nguyen Fernando Gomez-Pinilla Naiphinich Kotchabhakdi Jean De Vellis Araceli Espinosa-Jeffrey Jane & Terry Semel Institute for Neuroscience & Human Behavior Srinakharinwirot University University of California, Los Angeles University of Tokyo The Institute of Science and Technology for Research and Development, Mahidol University Biochemistry, Genetics and Molecular Biology © 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. 2018-12-11T02:19:25Z 2019-03-14T08:04:10Z 2018-12-11T02:19:25Z 2019-03-14T08:04:10Z 2016-02-17 Article Neurochemical Research. Vol.41, No.1-2 (2016), 431-449 10.1007/s11064-016-1850-z 15736903 03643190 2-s2.0-84958751578 https://repository.li.mahidol.ac.th/handle/123456789/43101 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84958751578&origin=inward |
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Biochemistry, Genetics and Molecular Biology Warin Krityakiarana Paul M. Zhao Kevin Nguyen Fernando Gomez-Pinilla Naiphinich Kotchabhakdi Jean De Vellis Araceli Espinosa-Jeffrey 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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© 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. |
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Jane & Terry Semel Institute for Neuroscience & Human Behavior |
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Jane & Terry Semel Institute for Neuroscience & Human Behavior Warin Krityakiarana Paul M. Zhao Kevin Nguyen Fernando Gomez-Pinilla Naiphinich Kotchabhakdi Jean De Vellis Araceli Espinosa-Jeffrey |
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Article |
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Warin Krityakiarana Paul M. Zhao Kevin Nguyen Fernando Gomez-Pinilla Naiphinich Kotchabhakdi Jean De Vellis Araceli Espinosa-Jeffrey |
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Warin Krityakiarana |
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 |
title_short |
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 |
title_full |
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 |
title_fullStr |
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 |
title_full_unstemmed |
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 |
title_sort |
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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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/43101 |
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1763493568535592960 |