Silk fibroin nanofibrous scaffolds incorporated with microRNA-222 loaded chitosan nanoparticles for enhanced neuronal differentiation of neural stem cells.

Carbohydr Polym

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, PR China; Biomedical Materials and Engineering Research Center of Hubei Province, Wuhan 430070, PR China. Electronic address:

Published: February 2022

AI Article Synopsis

  • Neural stem cells (NSCs) transplantation therapy shows potential for repairing neural tissue, but improving their differentiation into neurons remains a key challenge.
  • Researchers developed a method using microRNA-222 loaded chitosan nanoparticles (miR-222/CS NPs) combined with silk fibroin (SF) nanofibrous scaffolds to promote this differentiation.
  • The study found that these composite scaffolds effectively deliver miR-222 into NSCs and significantly enhance their neuronal development, indicating a promising strategy for neural tissue regeneration.

Article Abstract

Neural stem cells (NSCs) transplantation therapy is a promising method for neural tissue regeneration. How to enhance the neuronal differentiation of NSCs has been the most challenging aspect of NSCs application. Herein, the microRNA-222 loaded chitosan nanoparticles (miR-222/CS NPs) were incorporated with silk fibroin (SF) nanofibrous scaffolds to enhance neuronal differentiation of NSCs. The encapsulation efficiency of miR-222 in the miR-222/CS NPs was (96.4 ± 0.3) %. The results of the electrophoretic assay and cellular uptake assay confirmed that miR-222 was stable in the miR-222/CS NPs and can be effectively delivered into NSCs. The water contact angle decreased from (89 ± 3.05)° for the SF scaffolds to (14 ± 1.00)° for the composite scaffolds. The Western blot and RT-PCR results confirmed that the composite scaffolds could enhance neuronal differentiation of NSCs. In conclusion, the SF nanofibrous scaffolds in combination with miR-222/CS NPs are a promising approach for neural tissue regeneration.

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Source
http://dx.doi.org/10.1016/j.carbpol.2021.118791DOI Listing

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