TY - JOUR
T1 - Engineered 3D bioimplants using elastomeric scaffold, self-assembling peptide hydrogel, and adipose tissue-derived progenitor cells for cardiac regeneration
AU - Soler-Botija, Carolina
AU - Bagó, Juli R.
AU - Llucià-Valldeperas, Aida
AU - Vallés-Lluch, Ana
AU - Castells-Sala, Cristina
AU - Martínez-Ramos, Cristina
AU - Fernández-Muiños, Teresa
AU - Chachques, Juan Carlos
AU - Pradas, Manuel Monleón Pradas
AU - Semino, Carlos E.
AU - Bayes-Genis, Antoni
PY - 2014
Y1 - 2014
N2 - 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™), 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.
AB - 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™), 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.
KW - Cardiac regeneration
KW - Elastomeric membrane
KW - RECATABI
KW - Self-assembling peptide hydrogel
KW - Subcutaneous ATDPCs
UR - http://www.scopus.com/inward/record.url?scp=84901000464&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000338439400009&DestLinkType=FullRecord&DestApp=WOS_CPL
M3 - Article
C2 - 24936221
AN - SCOPUS:84901000464
SN - 1943-8141
VL - 6
SP - 291
EP - 301
JO - American Journal of Translational Research
JF - American Journal of Translational Research
IS - 3
ER -