Recombinant collagen scaffolds as substrates for human neural stem/progenitor cells
Autor: | Szu-Wen Wang, Nancy A. Da Silva, Richard Que, Lisa A. Flanagan, Janahan Arulmoli |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Materials science Integrin alpha1 Integrin Biomedical Engineering Article Epitope Biomaterials 03 medical and health sciences 0302 clinical medicine Coated Materials Biocompatible Neural Stem Cells Laminin Cell Adhesion Humans Progenitor cell Cell adhesion Cell Proliferation Integrin binding Neurons Tissue Scaffolds biology Integrin beta1 Metals and Alloys Cell Differentiation Recombinant Proteins Neural stem cell Cell biology 030104 developmental biology Astrocytes Ceramics and Composites biology.protein Collagen Stem cell 030217 neurology & neurosurgery |
Zdroj: | Journal of Biomedical Materials Research Part A. 106:1363-1372 |
ISSN: | 1552-4965 1549-3296 |
Popis: | Adhesion to the microenvironment profoundly affects stem cell functions, including proliferation and differentiation, and understanding the interaction of stem cells with the microenvironment is important for controlling their behavior. In this study, we investigated the effects of the integrin binding epitopes GFOGER and IKVAV (natively present in collagen I and laminin, respectively) on human neural stem/progenitor cells (hNSPCs). To test the specificity of these epitopes, GFOGER or IKVAV were placed within the context of recombinant triple-helical collagen III engineered to be devoid of native integrin binding sites. HNSPCs adhered to collagen that presented GFOGER as the sole integrin-binding site, but not to IKVAV-containing collagen. For the GFOGER-containing collagens, antibodies against the β1 integrin subunit prevented cellular adhesion, antibodies against the α1 subunit reduced cell adhesion, and antibodies against α2 or α3 subunits had no significant effect. These results indicate that hNSPCs primarily interact with GFOGER through the α1β1 integrin heterodimer. These GFOGER-presenting collagen variants also supported differentiation of hNSPCs into neurons and astrocytes. Our findings show, for the first time, that hNSPCs can bind to the GFOGER sequence, and they provide motivation to develop hydrogels formed from recombinant collagen variants as a cell delivery scaffold. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 1363-1372, 2018. |
Databáze: | OpenAIRE |
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