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A protein composite neural scaffold modulates astrocyte migration and transcriptome profile
Shippy, Teresa D. ; Brice, Ryan ; Yao, Li
Shippy, Teresa D.
Brice, Ryan
Yao, Li
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Adobe PDF, 2.75 MB
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Issue Date
2022-01-11
Type
Article
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Preprint
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Keywords
Astrocyte,Cell motility,Chondroitin sulfate proteoglycans,Glutenin,Neural scaffolds
Subjects (LCSH)
Citation
Yao, L., Brice, R. and Shippy, T. (2022), A Protein Composite Neural Scaffold Modulates Astrocyte Migration and Transcriptome Profile. Macromol. Biosci. 2100406. https://doi.org/10.1002/mabi.202100406
Abstract
Bioscaffold implantation is a promising approach to facilitate the repair and regeneration of wounded neural tissue after injury to the spinal cord or peripheral nerves. However, such bioscaffold grafts currently result in only limited functional recovery. The generation of a neural scaffold using a combination of collagen and glutenin is reported. The conduit material and mechanical properties, as well as its effect on astrocyte behavior is tested. After neural injuries, astrocytes move into the lesion and participate in the process of remodeling the micro-architecture of the wounded neural tissue. In this study, human astrocytes grown on glutenin-collagen scaffolds show higher motility and a lower proliferation rate compared with those grown on collagen scaffolds. RNA sequencing reveals that astrocytes grown on the two types of scaffolds show differentially expressed genes in Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways such as actin cytoskeleton and focal adhesion that regulate astrocyte migration on scaffolds. The gene expression of aggrecan and versican, chondroitin sulfate proteoglycans that inhibit axonal growth, is down-regulated in astrocytes grown on glutenin-collagen scaffolds. These outcomes indicate that the implantation of glutenin-collagen scaffolds may promote astrocyte function in the neural regeneration process by enhanced cell migration and reduced glial scar formation.
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Preprint from publisher. Also available from publisher's website at DOI.
Publisher
John Wiley & Sons, Ltd
Journal
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Series
Macromolecular Bioscience;2022
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ISSN
1616-5187
1616-5195
1616-5195
