| Literature DB >> 29744379 |
Martha I Betancur1, Hannah D Mason1, Melissa Alvarado-Velez2, Phillip V Holmes3, Ravi V Bellamkonda2, Lohitash Karumbaiah1.
Abstract
There are currently no effective treatments for moderate-to-severe traumatic brain injuries (TBIs). The paracrine functions of undifferentiated neural stem cells (NSCs) are believed to play a significant role in stimulating the repair and regeneration of injured brain tissue. We therefore hypothesized that fibroblast growth factor (FGF2) enriching chondroitin sulfate glycosaminoglycan (CS-GAG) matrices can maintain the undifferentiated state of neural stem cells (NSCs) and facilitate brain tissue repair subacutely post-TBI. Rats subjected to a controlled cortical impactor (CCI) induced TBI were intraparenchymally injected with CS-GAG matrices alone or with CS-GAG matrices containing PKH26GL labeled allogeneic NSCs. Nissl staining of brain tissue 4 weeks post-TBI demonstrated the significantly enhanced (p < 0.05) tissue protection in CS-GAG treated animals when compared to TBI only control, and NSC only treated animals. CS-GAG-NSC treated animals demonstrated significantly enhanced (p < 0.05) FGF2 retention, and maintenance of PKH26GL labeled NSCs as indicated by enhanced Sox1+ and Ki67+ cell presence over other differentiated cell types. Lastly, all treatment groups and sham controls exhibited a significantly (p < 0.05) attenuated GFAP+ reactive astrocyte presence in the lesion site when compared to TBI only controls.Entities:
Keywords: biomaterials; chondroitin sulfate glycosaminoglycan; hydrogels; neural stem cells; neuroprotection; traumatic brain injury
Year: 2017 PMID: 29744379 PMCID: PMC5937277 DOI: 10.1021/acsbiomaterials.6b00805
Source DB: PubMed Journal: ACS Biomater Sci Eng ISSN: 2373-9878