Epicardial application of cardiac progenitor cells in a 3D-printed gelatin/hyaluronic acid patch preserves cardiac function after myocardial infarction

被引:220
|
作者
Gaetani, Roberto [1 ,2 ,3 ,4 ]
Feyen, Dries A. M. [1 ]
Verhage, Vera [1 ]
Slaats, Rolf [1 ]
Messina, Elisa [2 ]
Christman, Karen L. [3 ,4 ]
Giacomello, Alessandro [2 ]
Doevendans, Pieter A. F. M. [1 ,5 ]
Sluijter, Joost P. G. [1 ,5 ]
机构
[1] Univ Med Ctr Utrecht, Dept Cardiol, DH&L, NL-3508 GA Utrecht, Netherlands
[2] Univ Roma La Sapienza, Dept Mol Med, Cenci Bolognetti Fdn, Inst Pasteur, I-00185 Rome, Italy
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Sanford Consortium Regenerat Med, La Jolla, CA 92093 USA
[5] Interuniv Cardiol Inst Netherlands ICIN, Utrecht, Netherlands
关键词
Cardiac progenitor cells; Tissue printing; Cardiac tissue engineering; Cardiac regeneration; Heart failure; CARDIOSPHERE-DERIVED CELLS; REGENERATION; THERAPY; CARDIOMYOCYTES; INTRACORONARY; HYDROGELS; STIFFNESS; MODEL;
D O I
10.1016/j.biomaterials.2015.05.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cardiac cell therapy suffers from limitations related to poor engraftment and significant cell death after transplantation. In this regard, ex vivo tissue engineering is a tool that has been demonstrated to increase cell retention and survival. The aim of our study was to evaluate the therapeutic potential of a 3D-printed patch composed of human cardiac-derived progenitor cells (hCMPCs) in a hyaluronic acid/gelatin (HA/gel) based matrix. hCMPCs were printed in the HA/gel matrix (30 x 10(6) cells/ml) to form a biocomplex made of six perpendicularly printed layers with a surface of 2 x 2 cm and thickness of 400 um, in which they retained their viability, proliferation and differentiation capability. The printed biocomplex was transplanted in a mouse model of myocardial infarction (MI). The application of the patch led to a significant reduction in adverse remodeling and preservation of cardiac performance as was shown by both MRI and histology. Furthermore, the matrix supported the long-term in vivo survival and engraftment of hCMPCs, which exhibited a temporal increase in cardiac and vascular differentiation markers over the course of the 4 week follow-up period. Overall, we developed an effective and translational approach to enhance hCMPC delivery and action in the heart. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:339 / 348
页数:10
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