Basic fibroblast growth factor promotes human dental pulp stem cells cultured in 3D porous chitosan scaffolds to neural differentiation. (3rd July 2021)

• Record Type: Journal Article
• Authors: Zheng, Ke; Feng, Guijuan; Zhang, Jinlong; Xing, Jing; Huang, Dan; Lian, Min; Zhang, Wei; Wu, Wenli; Hu, Yingzi; Lu, Xiaohui; Feng, Xingmei
• Is Part Of: International journal of neuroscience. Volume 131:Number 7(2021)
• Page Start: 625
• Page End: 633
• Publication Date: 2021-07-03
• Subjects: Dental pulp stem cells (DPSCs) -- bFGF -- chitosan scaffolds -- neural differentiation; Nervous system -- Periodicals; 612.805
• DOI: 10.1080/00207454.2020.1744592
• Languages: English
• ISSNs: 0020-7454

Abstract

Abstract: Aim/Purpose: Dental pulp stem cells (DPSCs) were widely used as seed cells in the field of tissue engineering and regenerative medicine, including spinal cord injury (SCI) repair and other neuronal degenerative diseases, due to their easy isolation, multiple differentiation potential, low immunogenicity and low rates of rejection during transplantation. Various studies have shown that bFGF can enhance peripheral nerve regeneration after injury, and phospho-ERK (p-ERK) activation as a major mediator may be involved in this process. Previous studies also have proved that a suitable biomaterial scaffold can carry and transport the therapeutic cells effectively to the recipient area. It has showed in our earlier experiments that 3D porous chitosan scaffolds exhibited a suitable circumstance for survival and neural differentiation of DPSCs in vitro . The purpose of the study was to evaluate the influence of chitosan scaffolds and bFGF on differentiation of DPSCs. Materials and methods: In current study, DPSCs were cultured in chitosan scaffolds and treated with neural differentiation medium for 7 days. The neural genes and protein markers were analyzed by western blot and immunofluorescence. Meanwhile, the relevant signaling pathway involved in this process was also tested. Results: Our study revealed that the viability of DPSCs was not influenced by co-culture with the chitosan scaffolds as well as bFGF. Compared with the control and DPSC/chitosan-scaffold groups, the levels of GFAP, S100β and β-tubulin III significantly increased in the DPSC/chitosan-scaffold+bFGF group. Conclusion: Chitosan scaffolds were non-cytotoxic to the survival of DPSCs, and chitosan scaffolds combined with bFGF facilitated the neural differentiation of DPSCs. The transplantation of DPSCs/chitosan-scaffold+bFGF might be a secure and effective method of treating SCI and other neuronal diseases.