Human adult heart harbors a population of resident progenitor cells that can be isolated by Sca-1 antibody and expanded in culture. These cells can differentiate into cardiomyocytes and vascular cells in vitro and contribute to cardiac regeneration in vivo. However, when directly injected as single cell suspension, the survival rate and retention is really poor, less than 1% of injected cells being detectable in the hosttissue within few weeks. The present study aimed at investigating the possibility to produce scaffoldless, thick cardiac progenitor cell-derived cardiac patches by thermo-responsive technology. Human cardiac progenitors obtained from the auricles of patients were cultured as scaffoldless engineered tissues fabricated using temperature-responsive surfaces obtained by poly-N-isopropylacrylamide (PNIPAAm) surface immobilization. In the engineered tissue, progenitor cells established proper three-dimensional intercellular relationships and produced abundant extracellular matrix, while preserving their phenotype and plasticity. Cell phenotype and viability within the 3D construct were followed for 1 week, showing that no significant differentiation or apoptotic events occurred within the construct. After engineered tissues were leant on visceral pericardium, a number of cells migrated into the myocardium and in the vascular walls, where they integrated in the respective textures. The study demonstrates the suitability of such approach to deliver stem cells.

Forte, G., Pietronave, S., Nardone, G., Zamperone, A., Pagliari, S., Pagliari, F., et al. (2012). Human cardiac progenitor cell sheets as a source of autologous contractile and vascular cells for cardiac repair. In 3rd TERMIS World Congress 2012, 5-8 September 2012, Vienna, Austria [10.1002/term.1586].

Human cardiac progenitor cell sheets as a source of autologous contractile and vascular cells for cardiac repair

MINIERI, MARILENA;DI NARDO, PAOLO
2012-09-03

Abstract

Human adult heart harbors a population of resident progenitor cells that can be isolated by Sca-1 antibody and expanded in culture. These cells can differentiate into cardiomyocytes and vascular cells in vitro and contribute to cardiac regeneration in vivo. However, when directly injected as single cell suspension, the survival rate and retention is really poor, less than 1% of injected cells being detectable in the hosttissue within few weeks. The present study aimed at investigating the possibility to produce scaffoldless, thick cardiac progenitor cell-derived cardiac patches by thermo-responsive technology. Human cardiac progenitors obtained from the auricles of patients were cultured as scaffoldless engineered tissues fabricated using temperature-responsive surfaces obtained by poly-N-isopropylacrylamide (PNIPAAm) surface immobilization. In the engineered tissue, progenitor cells established proper three-dimensional intercellular relationships and produced abundant extracellular matrix, while preserving their phenotype and plasticity. Cell phenotype and viability within the 3D construct were followed for 1 week, showing that no significant differentiation or apoptotic events occurred within the construct. After engineered tissues were leant on visceral pericardium, a number of cells migrated into the myocardium and in the vascular walls, where they integrated in the respective textures. The study demonstrates the suitability of such approach to deliver stem cells.
TERMIS World Congress
Vienna, Austria
2012
3rd
Rilevanza internazionale
contributo
3-set-2012
Settore BIO/10 - BIOCHIMICA
English
Intervento a convegno
Forte, G., Pietronave, S., Nardone, G., Zamperone, A., Pagliari, S., Pagliari, F., et al. (2012). Human cardiac progenitor cell sheets as a source of autologous contractile and vascular cells for cardiac repair. In 3rd TERMIS World Congress 2012, 5-8 September 2012, Vienna, Austria [10.1002/term.1586].
Forte, G; Pietronave, S; Nardone, G; Zamperone, A; Pagliari, S; Pagliari, F; Okano, T; Minieri, M; Prat, M; DI NARDO, P
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/101870
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact