IRIS – Institutional Research Information System
IRIS è il sistema di gestione della ricerca dell’Università degli Studi di Milano-Bicocca.Il repository BOA è il modulo del sistema dedicato alla raccolta e alla disseminazione della produzione scientifica di Ateneo. Le pubblicazioni sono ricercabili per parola chiave attraverso il box nella barra orizzontale in alto oppure, mediante il pulsante Sfoglia, per "Afferenza", "Autore", "Titolo", "Tipologia" o "Settore scientifico-disciplinare".
IRIS contiene inoltre alcuni moduli dedicati alla registrazione dei progetti e dei contratti, e alla reportistica avanzata per le attività di valutazione della ricerca
EnglishThe myocardium contains a resident progenitor cells, named cardiac progenitor cells, that maintain the heart homeostasis by replacing lost myocytes. The c-kit tyrosine kinase receptor is one of the principal markers defining cardiac progenitors in the adult mammalian heart, including human. C-kit+ cardiac progenitors have been recently identified as a multipotent cells population able to give rise to myocardial, endothelial and smooth muscle both in vitro and in vivo. The discovery of cardiac progenitors and the devise of culture systems to amplify these cells in culture without loosing their differentiation potency has opened new perspectives for clinical applications aimed at replacing myocardium lost as a consequence of acute or chronic ischemic disease. While cardiac progenitors have been deeply investigated for their stem cell activity, susceptibility to stress conditions and aging, and their ability to repair the infarcted heart, their origin, phenotype and biological features have been disclosed only in part. In the present study, we report that c-kit+ cardiac progenitors derived from the human heart express markers in common with mesenchymal stem cells. Our in vitro analyses revealed that, compared to bone marrow-derived mesenchymal cells, c-kit+ cardiac progenitors have a reduced ability to differentiate into canonical mesenchymal cellular derivatives such as osteoblasts and adipocytes; by contrast, under appropriate differentiation conditions, these cells gave rise to tubular-like structures at the same extent as endothelial cells, expressed smooth muscle cells markers, and expressed early and late myocardial markers. These findings suggest that ex-vivo amplified c-kit+ cardiac progenitors differentiate into mesenchymal cells having a preferentially myocardial commitment.
(2009). Isolation, characterization and ex vivo amplification of heart-derived c-kit progenitor cells for cellular therapy. (Tesi di dottorato, Università degli Studi di Milano-Bicocca, 2009).
| Autori: | ||
| Data di pubblicazione: | 26-nov-2009 | |
| Tutor esterno: | PESCE, MAURIZIO | |
| Titolo: | Isolation, characterization and ex vivo amplification of heart-derived c-kit progenitor cells for cellular therapy | |
| Settore Scientifico Disciplinare: | MED/11 - MALATTIE DELL'APPARATO CARDIOVASCOLARE | |
| Lingua: | English | |
| Scuola di dottorato: | Scuola di Dottorato in Medicina Traslazionale e Molecolare | |
| Corso di dottorato: | MEDICINA TRASLAZIONALE E MOLECOLARE (DIMET) - 45R | |
| Ciclo: | 22 | |
| Anno Accademico: | 2008/2009 | |
| Citazione: | (2009). Isolation, characterization and ex vivo amplification of heart-derived c-kit progenitor cells for cellular therapy. (Tesi di dottorato, Università degli Studi di Milano-Bicocca, 2009). | |
| Parole Chiave: | cardiac progenitor cells; Mesenchymal cells; cell culture; differentiation | |
| Appare nelle tipologie: | 07 - Tesi di dottorato Bicocca post 2009 |
File in questo prodotto:
| File | Descrizione | Tipologia | Licenza | |
|---|---|---|---|---|
| phd_unimib_031466.pdf | Doctoral thesis | Open Access Visualizza/Apri |
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