Enhanced growth and differentiation of neural stem cells on alginate/collagen/reduced graphene oxide composite hydrogel incorporated with lithium chloride

被引:2
|
作者
Babaei, Azadeh [1 ]
Tiraihi, Taki [1 ]
Ai, Jajar [2 ]
Baheiraei, Nafiseh [1 ]
机构
[1] Tarbiat Modares Univ, Fac Med Sci, Dept Anat Sci, Tehran, Iran
[2] Univ Tehran Med Sci, Sch Adv Technol Med, Dept Tissue Engn & Appl Cell Sci, Tehran, Iran
关键词
Spinal cord injury; Alginate; Collagen; Reduced graphene oxide; Injectable hydrogel; Neural stem cell; SPINAL-CORD; PROGENITOR CELLS; IN-VITRO; NEURONAL DIFFERENTIATION; DRUG-DELIVERY; ALGINATE HYDROGELS; TRANSPLANTATION; TISSUE; BRAIN; PROLIFERATION;
D O I
10.34172/bi.2023.24266
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Cell transplantation with hydrogel-based carriers is one of the advanced therapeutics for challenging diseases, such as spinal cord injury. Electrically conductive hydrogel has received much attention for its effect on nerve outgrowth and differentiation. Besides, a load of neuroprotective substances, such as lithium chloride can promote the differentiation properties of the hydrogel. Methods: In this study, alginate/ collagen/reduced graphene oxide hydrogel loaded with lithium chloride (AL/CO/rGO Li+) was prepared as an injectable cell delivery system for neural tissue regeneration. After determining the lithium-ion release profile, an MTT assay was performed to check neural viability. In the next step, real-time PCR was performed to evaluate the expression of cell adhesion and neurogenic markers. Results: Our results showed that the combination of collagen fibers and rGO with alginates increased cell viability and the gene expression of collagen-binding receptor subunits such as integrin alpha 1, and beta 1. Further, rGO contributed to the controlled release of lithium-ion hydrogel in terms of its plenty of negatively charged functional groups. The continuous culture of NSCs on AL/CO/rGO Li+ hydrogel increased neurogenic genes' expressions of nestin (5.9 fold), NF200 (36.8 fold), and synaptophysin (13.2 fold), as well as protein expression of NF200 and synaptophysin after about 14 days. Conclusion: The simultaneous ability of electrical conduction and lithium-ion release of AL/CO/rGO Li+ hydrogel could provide a favorable microenvironment for NSCs by improving their survival, maintaining cell morphology, and expressing the neural marker. It may be potentially used as a therapeutic approach for stem cell transplantation in a spinal cord injury.
引用
收藏
页码:475 / 487
页数:13
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