| Literature DB >> 27525311 |
Oscar Bartulos1,2, Zhen Wu Zhuang1, Yan Huang1, Nicole Mikush1, Carol Suh1,2, Alda Bregasi1, Lin Wang2,3, William Chang4, Diane S Krause2,3,5,6, Lawrence H Young1,7, Jordan S Pober6,8,9, Yibing Qyang1,2,6,9.
Abstract
Cardiovascular progenitor cells (CPCs) expressing the ISL1-LIM-homeodomain transcription factor contribute developmentally to cardiomyocytes in all 4 chambers of the heart. Here, we show that ISL1-CPCs can be applied to myocardial regeneration following injury. We used a rapid 3D methylcellulose approach to form murine and human ISL1-CPC spheroids that engrafted after myocardial infarction in murine hearts, where they differentiated into cardiomyocytes and endothelial cells, integrating into the myocardium and forming new blood vessels. ISL1-CPC spheroid-treated mice exhibited reduced infarct area and increased blood vessel formation compared with control animals. Moreover, left ventricular (LV) contractile function was significantly better in mice transplanted with ISL1-CPCs 4 weeks after injury than that in control animals. These results provide proof-of-concept of a cardiac repair strategy employing ISL1-CPCs that, based on our previous lineage-tracing studies, are committed to forming heart tissue, in combination with a robust methylcellulose spheroid-based delivery approach.Entities:
Year: 2016 PMID: 27525311 PMCID: PMC4982472 DOI: 10.1172/jci.insight.80920
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708