4.6 Article

Prolonged survival of transplanted stem cells after ischaemic injury via the slow release of pro-survival peptides from a collagen matrix

Journal

NATURE BIOMEDICAL ENGINEERING
Volume 2, Issue 2, Pages 104-113

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41551-018-0191-4

Keywords

-

Funding

  1. Stanford Bio-X
  2. National Institutes of Health [HL133272, HL132875, 113006, EB009035, HL134830-01]
  3. California Institute of Regenerative Medicine (CIRM) [DR2-05394, RT3-07798]

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available