Engineered 3D bioimplants using elastomeric scaffold, self-assembling peptide hydrogel, and adipose tissue-derived progenitor cells for cardiac regeneration

被引:0
|
作者
Soler-Botija, Carolina [1 ]
Bago, Juli R. [2 ]
Llucia-Valldeperas, Aida [1 ]
Valles-Lluch, Ana [3 ]
Castells-Sala, Cristina [4 ]
Martinez-Ramos, Cristina [3 ]
Fernandez-Muinos, Teresa [4 ]
Chachques, Juan Carlos [5 ]
Monleon Pradas, Manuel [3 ]
Semino, Carlos E. [4 ]
Bayes-Genis, Antoni [1 ,6 ]
机构
[1] Hosp Badalona Germans Trias & Pujol, Serv Cardiol, Hlth Res Inst Germans Trias & Pujol IGTP, Heart Failure & Cardiac Regenerat ICREC Res Progr, Badalona 08916, Barcelona, Spain
[2] Univ N Carolina, UNC Eshelman Sch Pharm, Div Mol Pharmaceut, Chapel Hill, NC USA
[3] Univ Politecn Valencia, Ctr Biomat & Tissue Engn, E-46071 Valencia, Spain
[4] Ramon Llull Univ, IQS Sch Engn, Dept Bioengn, Barcelona, Spain
[5] Pompidou Hosp, Dept Cardiovasc Surg, Paris, France
[6] Autonomous Univ Barcelona, Dept Med, E-08193 Barcelona, Spain
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2014年 / 6卷 / 03期
关键词
Cardiac regeneration; subcutaneous ATDPCs; self-assembling peptide hydrogel; elastomeric membrane; RECATABI; ACUTE MYOCARDIAL-INFARCTION; MESENCHYMAL STEM-CELLS; CARDIOMYOCYTE RENEWAL; CONTROLLED-TRIAL; IN-VITRO; DIFFERENTIATION; TRANSPLANTATION; BIOMATERIALS; IMPROVEMENT; EXPANSION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Contractile restoration of myocardial scars remains a challenge with important clinical implications. Here, a combination of porous elastomeric membrane, peptide hydrogel, and subcutaneous adipose tissue-derived progenitor cells (subATDPCs) was designed and evaluated as a bioimplant for cardiac regeneration in a mouse model of myocardial infarction. SubATDPCs were doubly transduced with lentiviral vectors to express bioluminescent-fluorescent reporters driven by constitutively active, cardiac tissue-specific promoters. Cells were seeded into an engineered bioimplant consisting of a scaffold (polycaprolactone methacryloyloxyethyl ester) filled with a peptide hydrogel (PuraMatrix(TM)), and transplanted to cover injured myocardium. Bioluminescence and fluorescence quantifications showed de novo and progressive increases in promoter expression in bioactive implant-treated animals. The bioactive implant was well adapted to the heart, and fully functional vessels traversed the myocardium-bioactive implant interface. Treatment translated into a detectable positive effect on cardiac function, as revealed by echocardiography. Thus, this novel implant is a promising construct for supporting myocardial regeneration.
引用
收藏
页码:291 / 301
页数:11
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