Tissue-Engineered Vascular Grafts with Advanced Mechanical Strength from Human iPSCs

被引:113
作者
Luo, Jiesi [1 ,2 ]
Qin, Lingfeng [3 ]
Zhao, Liping [4 ,5 ]
Gui, Liqiong [4 ,5 ]
Ellis, Matthew W. [1 ,2 ,6 ]
Huang, Yan [1 ,2 ]
Kural, Mehmet H. [4 ,5 ]
Clark, J. Alexander [7 ]
Ono, Shun [3 ,4 ]
Wang, Juan [4 ,5 ]
Yuan, Yifan [4 ,5 ]
Zhang, Shang-Min [8 ]
Cong, Xiaoqiang [1 ,2 ,9 ]
Li, Guangxin [3 ,10 ]
Riaz, Muhammad [1 ,2 ]
Lopez, Colleen [1 ,2 ]
Hotta, Akitsu [11 ]
Campbell, Stuart [7 ]
Tellides, George [3 ,4 ]
Dardik, Alan [3 ,4 ]
Niklason, Laura E. [2 ,4 ,5 ,7 ]
Qyang, Yibing [1 ,2 ,4 ,8 ]
机构
[1] Yale Sch Med, Yale Cardiovasc Res Ctr, Dept Internal Med, Sect Cardiovasc Med, New Haven, CT 06511 USA
[2] Yale Stem Cell Ctr, New Haven, CT 06520 USA
[3] Yale Univ, Dept Surg, New Haven, CT 06520 USA
[4] Yale Univ, Vasc Biol & Therapeut Program, Sch Med, New Haven, CT 06520 USA
[5] Yale Univ, Dept Anesthesiol, New Haven, CT 06519 USA
[6] Yale Univ, Dept Cellular & Mol Physiol, New Haven, CT 06519 USA
[7] Yale Univ, Dept Biomed Engn, New Haven, CT 06519 USA
[8] Yale Sch Med, Dept Pathol, New Haven, CT 06520 USA
[9] Bethune First Hosp Jilin Univ, Dept Cardiol, Changchun 130021, Peoples R China
[10] China Med Univ, Dept Vasc Surg, Hosp 1, Shenyang 110122, Liaoning, Peoples R China
[11] Kyoto Univ, Ctr iPS Cell Res & Applicat CiRA, Kyoto 6068501, Japan
关键词
SMOOTH-MUSCLE-CELLS; PLURIPOTENT STEM-CELLS; BLOOD-VESSELS; GENERATION; COLLAGEN; ACCESS; BETA;
D O I
10.1016/j.stem.2019.12.012
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:251 / +
页数:19
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