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Prolonged survival of transplanted stem cells after ischaemic injury via the slow release of pro-survival peptides from a collagen matrix
- Lee, Andrew S;
- Inayathullah, Mohammed;
- Lijkwan, Maarten A;
- Zhao, Xin;
- Sun, Wenchao;
- Park, Sujin;
- Hong, Wan Xing;
- Parekh, Mansi B;
- Malkovskiy, Andrey V;
- Lau, Edward;
- Qin, Xulei;
- Pothineni, Venkata Raveendra;
- Sanchez-Freire, Verónica;
- Zhang, Wendy Y;
- Kooreman, Nigel G;
- Ebert, Antje D;
- Chan, Charles KF;
- Nguyen, Patricia K;
- Rajadas, Jayakumar;
- Wu, Joseph C
Published Web Location
https://doi.org/10.1038/s41551-018-0191-4Abstract
Stem-cell-based therapies hold considerable promise for regenerative medicine. However, acute donor-cell death within several weeks after cell delivery remains a critical hurdle for clinical translation. Co-transplantation of stem cells with pro-survival factors can improve cell engraftment, but this strategy has been hampered by the typically short half-lives of the factors and by the use of Matrigel and other scaffolds that are not chemically defined. Here, we report a collagen-dendrimer biomaterial crosslinked with pro-survival peptide analogues that adheres to the extracellular matrix and slowly releases the peptides, significantly prolonging stem cell survival in mouse models of ischaemic injury. The biomaterial can serve as a generic delivery system to improve functional outcomes in cell-replacement therapy.
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