| Literature DB >> 31956039 |
Jiesi Luo1, Lingfeng Qin2, Liping Zhao3, Liqiong Gui3, Matthew W Ellis4, Yan Huang1, Mehmet H Kural3, J Alexander Clark5, Shun Ono6, Juan Wang3, Yifan Yuan3, Shang-Min Zhang7, Xiaoqiang Cong8, Guangxin Li9, Muhammad Riaz1, Colleen Lopez1, Akitsu Hotta10, Stuart Campbell5, George Tellides6, Alan Dardik6, Laura E Niklason11, Yibing Qyang12.
Abstract
Vascular smooth muscle cells (VSMCs) can be derived in large numbers from human induced pluripotent stem cells (hiPSCs) for producing tissue-engineered vascular grafts (TEVGs). However, hiPSC-derived TEVGs are hampered by low mechanical strength and significant radial dilation after implantation. Here, we report generation of hiPSC-derived TEVGs with mechanical strength comparable to native vessels used in arterial bypass grafts by utilizing biodegradable scaffolds, incremental pulsatile stretching, and optimal culture conditions. Following implantation into a rat aortic model, hiPSC-derived TEVGs show excellent patency without luminal dilation and effectively maintain mechanical and contractile function. This study provides a foundation for future production of non-immunogenic, cellularized hiPSC-derived TEVGs composed of allogenic vascular cells, potentially serving needs to a considerable number of patients whose dysfunctional vascular cells preclude TEVG generation via other methods.Entities:
Keywords: human induced pluripotent stem cells; tissue engineered vascular grafts; vascular smooth muscle cells
Mesh:
Year: 2020 PMID: 31956039 PMCID: PMC7021512 DOI: 10.1016/j.stem.2019.12.012
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633