Authors
Chao Han, Shuna Chen, Zihan Shi, Xin Guan, Wei Zou, Jing Liu
Published in
Neural regeneration research. Volume 21. Issue 7. Pages 3017-3025. Jul 01, 2026. Epub Jun 19, 2025.
Abstract
Stem cell therapy shows promise for treating brain injuries; neural stem cells in particular are capable of repairing damage by forming new nerve cells and supporting recovery. However, optimizing the implantation and functionality of these cells in damaged brain regions remains challenging. Silk fibroin, a natural protein derived from silkworm silk, is a biocompatible material with exceptional properties that are useful for tissue engineering. Its biodegradability, mechanical robustness, and ability to promote cell growth make it particularly valuable for biomedical applications. Silk fibroin nanomaterials, which comprise silk fibroin processed into nanostructures, offer enhanced surface area, improved loading capacity for bioactive molecules, and superior nanoscale interactions with cells compared with bulk silk fibroin materials. In this study, we first extracted human-derived neural stem cells from a 14-week-old human fetus. Then, neural stem cells were loaded with 1% silk fibroin nanomaterials, which was identified as the optimal concentration to support human-derived neural stem cell growth and release of neurotrophic factors. Finally, 1% silk fibroin nanomaterials were implanted into a rat model of hypoxic-ischemic brain injury. The results showed that, compared with the treatment with human-derived neural stem cells alone, silk fibroin hydrogel carrying human-derived neural stem cells was significantly more effective at alleviating brain tissue damage, increasing neurotrophic factor secretion in the brain microenvironment, and promoting motor and cognitive function recovery. These findings suggest that silk fibroin nanomaterials loaded with human-derived neural stem cells could be used to treat hypoxic-ischemic encephalopathy. However, the mechanisms and related signaling pathways by which hydrogels combined with cells exert their reparative effects still require further in-depth investigation.
PMID:
40537000
Bibliographic data and abstract were imported from PubMed on 13 Sep 2026.
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