Local Delivery of Taxol From FGL-Functionalized Self-Assembling Peptide Nanofiber Scaffold Promotes Recovery After Spinal Cord Injury

Taxol has been clinically approved as an antitumor drug, and it exerts its antitumor effect through the excessive stabilization of microtubules in cancer cells. Recently, moderate microtubule stabilization by Taxol has been shown to efficiently promote neurite regeneration and functional recovery af...

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Published inFrontiers in cell and developmental biology Vol. 8; p. 820
Main Authors Xiao, Zhiyong, Yao, Yingtao, Wang, Zhiyu, Tian, Qing, Wang, Jiedong, Gu, Li, Li, Bo, Zheng, Qixin, Wu, Yongchao
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 21.08.2020
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Summary:Taxol has been clinically approved as an antitumor drug, and it exerts its antitumor effect through the excessive stabilization of microtubules in cancer cells. Recently, moderate microtubule stabilization by Taxol has been shown to efficiently promote neurite regeneration and functional recovery after spinal cord injury (SCI). However, the potential for the clinical translation of Taxol in treating SCI is limited by its side effects and low ability to cross the blood-spinal cord barrier (BSCB). Self-assembled peptide hydrogels have shown potential as drug carriers for the local delivery of therapeutic agents. We therefore hypothesized that the localized delivery of Taxol by a self-assembled peptide scaffold would promote axonal regeneration by stabilizing microtubules during the treatment of SCI. In the present study, the mechanistic functions of the Taxol-releasing system were clarified in vitro and in vivo using immunofluorescence labeling, histology and neurobehavioral analyses. Based on the findings from the in vitro study, Taxol released from a biological functionalized SAP nanofiber scaffold (FGLmx/Taxol) remained active and promoted neurite extension. In this study, we used a weight-drop contusion model to induce SCI at T9. The local delivery of Taxol from FGLmx/Taxol significantly decreased glial scarring and increased the number of nerve fibers compared with the use of FGLmx and 5% glucose. Furthermore, animals administered FGLmx/Taxol exhibited neurite preservation, smaller cavity dimensions, and decreased inflammation and demyelination. Thus, the local delivery of Taxol from FGLmx/Taxol was effective at promoting recovery after SCI and has potential as a new therapeutic strategy for SCI.
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This article was submitted to Cell Death and Survival, a section of the journal Frontiers in Cell and Developmental Biology
Edited by: Guangyong Peng, Saint Louis University, United States
These authors have contributed equally to this work
Present address: Zhiyong Xiao, Department of Orthopaedics, Wuhan Third Hospital, Tongren Hospital of Wuhan University, Wuhan, China
Reviewed by: Chunying Li, Georgia State University, United States; Jun Xu, Beijing Tiantan Hospital, Capital Medical University, China
ISSN:2296-634X
2296-634X
DOI:10.3389/fcell.2020.00820