Tang Junnan, Su Teng, Huang Ke, Dinh Phuong-Uyen, Wang Zegen, Vandergriff Adam, Hensley Michael T, Cores Jhon, Allen Tyler, Li Taosheng, Sproul Erin, Mihalko Emily, Lobo Leonard J, Ruterbories Laura, Lynch Alex, Brown Ashley, Caranasos Thomas G, Shen Deliang, Stouffer George A, Gu Zhen, Zhang Jinying, Cheng Ke
Department of Molecular Biomedical Sciences and Comparative Medicine Institute, North Carolina State University, Raleigh, NC, USA.
Joint Department of Biomedical Engineering and Comparative Medicine Institute, University of North Carolina at Chapel Hill & North Carolina State University, Raleigh, NC, USA.
Nat Biomed Eng. 2018;2:17-26. doi: 10.1038/s41551-017-0182-x. Epub 2018 Jan 10.
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.
临床应用的干细胞移植存在移植细胞保留率低和植入率低的问题。受血小板将干细胞募集到血管损伤部位能力的启发,我们推测血小板可能会增强心脏干细胞(CSCs)向心肌梗死损伤部位的血管递送。在此,我们表明,表面膜融合有血小板纳米囊泡的CSCs表达与血小板粘附于损伤部位相关的血小板表面标志物。我们还发现,修饰后的CSCs选择性地结合胶原包被的表面和内皮剥脱的大鼠主动脉,并且在大鼠和猪急性心肌梗死模型中,修饰后的CSCs增加了在心脏中的保留率并减小了梗死面积。因此,血小板纳米囊泡融合的CSCs具有其亲代细胞类型的天然靶向和修复能力。这种干细胞操作方法快速、直接且安全,不需要对细胞进行基因改造,并且应该可以推广到多种细胞类型。