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Rapamycin promotes Schwann cell migration and nerve growth factor secretion

Rapamycin, similar to FK506, can promote neural regeneration in vitro. We assumed that the mechanisms of action of rapamycin and FK506 in promoting peripheral nerve regeneration were similar. This study compared the effects of different concentrations of rapamycin and FK506 on Schwann cells and inve...

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Autores principales: Liu, Fang, Zhang, Haiwei, Zhang, Kaiming, Wang, Xinyu, Li, Shipu, Yin, Yixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4146242/
https://www.ncbi.nlm.nih.gov/pubmed/25206862
http://dx.doi.org/10.4103/1673-5374.130101
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author Liu, Fang
Zhang, Haiwei
Zhang, Kaiming
Wang, Xinyu
Li, Shipu
Yin, Yixia
author_facet Liu, Fang
Zhang, Haiwei
Zhang, Kaiming
Wang, Xinyu
Li, Shipu
Yin, Yixia
author_sort Liu, Fang
collection PubMed
description Rapamycin, similar to FK506, can promote neural regeneration in vitro. We assumed that the mechanisms of action of rapamycin and FK506 in promoting peripheral nerve regeneration were similar. This study compared the effects of different concentrations of rapamycin and FK506 on Schwann cells and investigated effects and mechanisms of rapamycin on improving peripheral nerve regeneration. Results demonstrated that the lowest rapamycin concentration (1.53 nmol/L) more significantly promoted Schwann cell migration than the highest FK506 concentration (100μmol/L). Rapamycin promoted the secretion of nerve growth factors and upregulated growth-associated protein 43 expression in Schwann cells, but did not significantly affect Schwann cell proliferation. Therefore, rapamycin has potential application in peripheral nerve regeneration therapy.
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spelling pubmed-41462422014-09-09 Rapamycin promotes Schwann cell migration and nerve growth factor secretion Liu, Fang Zhang, Haiwei Zhang, Kaiming Wang, Xinyu Li, Shipu Yin, Yixia Neural Regen Res Research and Report Rapamycin, similar to FK506, can promote neural regeneration in vitro. We assumed that the mechanisms of action of rapamycin and FK506 in promoting peripheral nerve regeneration were similar. This study compared the effects of different concentrations of rapamycin and FK506 on Schwann cells and investigated effects and mechanisms of rapamycin on improving peripheral nerve regeneration. Results demonstrated that the lowest rapamycin concentration (1.53 nmol/L) more significantly promoted Schwann cell migration than the highest FK506 concentration (100μmol/L). Rapamycin promoted the secretion of nerve growth factors and upregulated growth-associated protein 43 expression in Schwann cells, but did not significantly affect Schwann cell proliferation. Therefore, rapamycin has potential application in peripheral nerve regeneration therapy. Medknow Publications & Media Pvt Ltd 2014-03-15 /pmc/articles/PMC4146242/ /pubmed/25206862 http://dx.doi.org/10.4103/1673-5374.130101 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research and Report
Liu, Fang
Zhang, Haiwei
Zhang, Kaiming
Wang, Xinyu
Li, Shipu
Yin, Yixia
Rapamycin promotes Schwann cell migration and nerve growth factor secretion
title Rapamycin promotes Schwann cell migration and nerve growth factor secretion
title_full Rapamycin promotes Schwann cell migration and nerve growth factor secretion
title_fullStr Rapamycin promotes Schwann cell migration and nerve growth factor secretion
title_full_unstemmed Rapamycin promotes Schwann cell migration and nerve growth factor secretion
title_short Rapamycin promotes Schwann cell migration and nerve growth factor secretion
title_sort rapamycin promotes schwann cell migration and nerve growth factor secretion
topic Research and Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4146242/
https://www.ncbi.nlm.nih.gov/pubmed/25206862
http://dx.doi.org/10.4103/1673-5374.130101
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