Bioinspired nanofiber scaffold for differentiating bone marrow-derived neural stem cells to oligodendrocyte-like cells : design, fabrication, and characterization |
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Author: | Boroojeni, Fatemeh Rasti1,2; Mashayekhan, Shohreh1; Abbaszadeh, Hojjat-Allah3,4; |
Organizations: |
1Department of Chemical and Petroleum Engineering, Sharif University of Technology, Tehran, Iran 2Division of Molecular Physics, Department of Physics, Chemistry and Biology, Linköping University, Linköping, Sweden 3Hearing Disorders Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
4Laser Application in Medical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
5Biocenter Oulu, Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland 6Sina Trauma and Surgery Research Center, Tehran University of Medical Sciences, Tehran, Iran |
Format: | article |
Version: | published version |
Access: | open |
Online Access: | PDF Full Text (PDF, 9.2 MB) |
Persistent link: | http://urn.fi/urn:nbn:fi-fe2020071047202 |
Language: | English |
Published: |
Dove Medical Press,
2020
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Publish Date: | 2020-07-10 |
Description: |
AbstractBackground: Researchers are trying to study the mechanism of neural stem cells (NSCs) differentiation to oligodendrocyte-like cells (OLCs) as well as to enhance the selective differentiation of NSCs to oligodendrocytes. However, the limitation in nerve tissue accessibility to isolate the NSCs as well as their differentiation toward oligodendrocytes is still challenging. Purpose: In the present study, a hybrid polycaprolactone (PCL)-gelatin nanofiber scaffold mimicking the native extracellular matrix and axon morphology to direct the differentiation of bone marrow-derived NSCs to OLCs was introduced. Materials and Methods: In order to achieve a sustained release of T3, this factor was encapsulated within chitosan nanoparticles and chitosan-loaded T3 was incorporated within PCL nanofibers. Polyaniline graphene (PAG) nanocomposite was incorporated within gelatin nanofibers to endow the scaffold with conductive properties, which resemble the conductive behavior of axons. Biodegradation, water contact angle measurements, and scanning electron microscopy (SEM) observations as well as conductivity tests were used to evaluate the properties of the prepared scaffold. The concentration of PAG and T3-loaded chitosan NPs in nanofibers were optimized by examining the proliferation of cultured bone marrow-derived mesenchymal stem cells (BMSCs) on the scaffolds. The differentiation of BMSCs-derived NSCs cultured on the fabricated scaffolds into OLCs was analyzed by evaluating the expression of oligodendrocyte markers using immunofluorescence (ICC), RT-PCR and flowcytometric assays. Results: Incorporating 2% PAG proved to have superior cell support and proliferation while guaranteeing electrical conductivity of 10.8 × 10− 5 S/cm. Moreover, the scaffold containing 2% of T3-loaded chitosan NPs was considered to be the most biocompatible samples. Result of ICC, RT-PCR and flow cytometry showed high expression of O4, Olig2, platelet-derived growth factor receptor-alpha (PDGFR-α), O1, myelin/oligodendrocyte glycoprotein (MOG) and myelin basic protein (MBP) high expressed but low expression of glial fibrillary acidic protein (GFAP). Conclusion: Considering surface topography, biocompatibility, electrical conductivity and gene expression, the hybrid PCL/gelatin scaffold with the controlled release of T3 may be considered as a promising candidate to be used as an in vitro model to study patient-derived oligodendrocytes by isolating patient’s BMSCs in pathological conditions such as diseases or injuries. Moreover, the resulted oligodendrocytes can be used as a desirable source for transplanting in patients. see all
See correctionRasti Boroojeni F, Mashayekhan S, Abbaszadeh HA, Ansarizadeh M, Khoramgah MS, Rahimi Movaghar V. Bioinspired Nanofiber Scaffold for Differentiating Bone Marrow-Derived Neural Stem Cells to Oligodendrocyte-Like Cells: Design, Fabrication, and Characterization [Corrigendum]. Int J Nanomedicine. 2020;15:6085-6088, https://doi.org/10.2147/IJN.S271954 see all
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Series: |
International journal of nanomedicine |
ISSN: | 1176-9114 |
ISSN-E: | 1178-2013 |
ISSN-L: | 1176-9114 |
Volume: | 15 |
Pages: | 3903 - 3920 |
DOI: | 10.2147/IJN.S248509 |
OADOI: | https://oadoi.org/10.2147/IJN.S248509 |
Type of Publication: |
A1 Journal article – refereed |
Field of Science: |
217 Medical engineering 221 Nanotechnology |
Subjects: | |
Copyright information: |
© 2020 Rasti Boroojeni et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License. By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms. |
https://creativecommons.org/licenses/by-nc/3.0/ |