| Literature DB >> 29862136 |
Junnan Tang1,2,3, Teng Su1,2, Ke Huang1, Phuong-Uyen Dinh1, Zegen Wang4, Adam Vandergriff1,2, Michael T Hensley1,2, Jhon Cores1,2, Tyler Allen1, Taosheng Li5, Erin Sproul2, Emily Mihalko2, Leonard J Lobo6, Laura Ruterbories7, Alex Lynch7, Ashley Brown2, Thomas G Caranasos8, Deliang Shen1,2,3, George A Stouffer9, Zhen Gu2, Jinying Zhang3, Ke Cheng10,11,12,13.
Abstract
Stem cell transplantation, as used clinically, suffers from low retention and engraftment of the transplanted cells. Inspired by the ability of platelets to recruit stem cells to sites of injury on blood vessels, we hypothesized that platelets might enhance the vascular delivery of cardiac stem cells (CSCs) to sites of myocardial infarction injury. Here, we show that CSCs with platelet nanovesicles fused onto their surface membranes express platelet surface markers that are associated with platelet adhesion to injury sites. We also find that the modified CSCs selectively bind collagen-coated surfaces and endothelium-denuded rat aortas, and that in rat and porcine models of acute myocardial infarction the modified CSCs increase retention in the heart and reduce infarct size. Platelet-nanovesicle-fused CSCs thus possess the natural targeting and repairing ability of their parental cell types. This stem cell manipulation approach is fast, straightforward and safe, does not require genetic alteration of the cells, and should be generalizable to multiple cell types.Entities:
Year: 2018 PMID: 29862136 PMCID: PMC5976251 DOI: 10.1038/s41551-017-0182-x
Source DB: PubMed Journal: Nat Biomed Eng ISSN: 2157-846X Impact factor: 25.671