Microfiber drug/gene delivery platform for study of myelination
Our ability to rescue functional deficits after demyelinating diseases or spinal cord injuries is limited by our lack of understanding of the complex remyelination process, which is crucial to functional recovery. In this study, we developed an electrospun suspended poly(ε-caprolactone) microfiber p...
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sg-ntu-dr.10356-898192020-11-01T04:44:13Z Microfiber drug/gene delivery platform for study of myelination Ong, William Lin, Junquan Bechler, Marie E. Wang, Kai Wang, Mingfeng ffrench-Constant, Charles Chew, Sing Yian School of Chemical and Biomedical Engineering Interdisciplinary Graduate School (IGS) Lee Kong Chian School of Medicine (LKCMedicine) Electrospinning RNA Interference DRNTU::Science::Medicine::Biomedical engineering Our ability to rescue functional deficits after demyelinating diseases or spinal cord injuries is limited by our lack of understanding of the complex remyelination process, which is crucial to functional recovery. In this study, we developed an electrospun suspended poly(ε-caprolactone) microfiber platform to enable the screening of therapeutics for remyelination. As a proof of concept, this platform employed scaffold-mediated non-viral delivery of a microRNA (miR) cocktail to promote oligodendrocyte precursor cells (OPCs) differentiation and myelination. We observed enhanced OPCs differentiation when the cells were transfected with miR-219 and miR-338 on the microfiber substrates. Moreover, miRs promoted the formation of MBP+ tubular extensions around the suspended fibers, which was indicative of myelination, instead of flat myelin membranes on 2D substrates. In addition, OPCs that were transfected with the cocktail of miRs formed significantly longer and larger amounts of MBP+ extensions. Taken together, these results demonstrate the efficacy of this functional screening platform for understanding myelination. MOE (Min. of Education, S’pore) NMRC (Natl Medical Research Council, S’pore) Accepted version 2018-10-29T01:45:48Z 2019-12-06T17:34:13Z 2018-10-29T01:45:48Z 2019-12-06T17:34:13Z 2018 Journal Article Ong, W., Lin, J., Bechler, M. E., Wang, K., Wang, M., ffrench-Constant, C., & Chew, S. Y. (2018). Microfiber drug/gene delivery platform for study of myelination. Acta Biomaterialia, 75152-160. doi:10.1016/j.actbio.2018.06.011 1742-7061 https://hdl.handle.net/10356/89819 http://hdl.handle.net/10220/46451 10.1016/j.actbio.2018.06.011 en Acta Biomaterialia © 2018 Elsevier. This is the author created version of a work that has been peer reviewed and accepted for publication by Acta Biomaterialia, Elsevier. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http:dx.doi.org/10.1016/j.actbio.2018.06.011]. 33 p. application/pdf |
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Electrospinning RNA Interference DRNTU::Science::Medicine::Biomedical engineering Ong, William Lin, Junquan Bechler, Marie E. Wang, Kai Wang, Mingfeng ffrench-Constant, Charles Chew, Sing Yian Microfiber drug/gene delivery platform for study of myelination |
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Our ability to rescue functional deficits after demyelinating diseases or spinal cord injuries is limited by our lack of understanding of the complex remyelination process, which is crucial to functional recovery. In this study, we developed an electrospun suspended poly(ε-caprolactone) microfiber platform to enable the screening of therapeutics for remyelination. As a proof of concept, this platform employed scaffold-mediated non-viral delivery of a microRNA (miR) cocktail to promote oligodendrocyte precursor cells (OPCs) differentiation and myelination. We observed enhanced OPCs differentiation when the cells were transfected with miR-219 and miR-338 on the microfiber substrates. Moreover, miRs promoted the formation of MBP+ tubular extensions around the suspended fibers, which was indicative of myelination, instead of flat myelin membranes on 2D substrates. In addition, OPCs that were transfected with the cocktail of miRs formed significantly longer and larger amounts of MBP+ extensions. Taken together, these results demonstrate the efficacy of this functional screening platform for understanding myelination. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Ong, William Lin, Junquan Bechler, Marie E. Wang, Kai Wang, Mingfeng ffrench-Constant, Charles Chew, Sing Yian |
format |
Article |
author |
Ong, William Lin, Junquan Bechler, Marie E. Wang, Kai Wang, Mingfeng ffrench-Constant, Charles Chew, Sing Yian |
author_sort |
Ong, William |
title |
Microfiber drug/gene delivery platform for study of myelination |
title_short |
Microfiber drug/gene delivery platform for study of myelination |
title_full |
Microfiber drug/gene delivery platform for study of myelination |
title_fullStr |
Microfiber drug/gene delivery platform for study of myelination |
title_full_unstemmed |
Microfiber drug/gene delivery platform for study of myelination |
title_sort |
microfiber drug/gene delivery platform for study of myelination |
publishDate |
2018 |
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https://hdl.handle.net/10356/89819 http://hdl.handle.net/10220/46451 |
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1683493175558144000 |