Activation of endogenous neurogenesis and angiogenesis by basic fibroblast growth factor-chitosan gel in an adult rat model of ischemic stroke
JOURNAL/nrgr/04.03/01300535-202402000-00035/inline-graphic1/v/2023-07-19T141749Z/r/image-tiff Attempts have been made to use cell transplantation and biomaterials to promote cell proliferation, differentiation, migration, and survival, as well as angiogenesis, in the context of brain injury. However...
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Summary: | JOURNAL/nrgr/04.03/01300535-202402000-00035/inline-graphic1/v/2023-07-19T141749Z/r/image-tiff
Attempts have been made to use cell transplantation and biomaterials to promote cell proliferation, differentiation, migration, and survival, as well as angiogenesis, in the context of brain injury. However, whether bioactive materials can repair the damage caused by ischemic stroke by activating endogenous neurogenesis and angiogenesis is still unknown. In this study, we applied chitosan gel loaded with basic fibroblast growth factor to the stroke cavity 7 days after ischemic stroke in rats. The gel slowly released basic fibroblast growth factor, which improved the local microenvironment, activated endogenous neural stem/progenitor cells, and recruited these cells to migrate toward the penumbra and stroke cavity and subsequently differentiate into neurons, while enhancing angiogenesis in the penumbra and stroke cavity and ultimately leading to partial functional recovery. This study revealed the mechanism by which bioactive materials repair ischemic strokes, thus providing a new strategy for the clinical application of bioactive materials in the treatment of ischemic stroke. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Both authors contributed equally to this article. Author contributions: XL, ZY, HD designed the study. XL, ZY, HD, SL, PH, FH, WZ, YG, XB and YG carried out experiments or provided critical reagents and protocols. HD, SL, HQ and YL analyzed the data and performed statistical analyses. ZY, HD, SL, KC, KFS and XL wrote the manuscript. All authors approved the final version of the manuscript. |
ISSN: | 1673-5374 1876-7958 |
DOI: | 10.4103/1673-5374.375344 |