OPLA Scaffold, Collagen I, and Horse Serum Induce a Higher Degree of Myogenic Differentiation of Adult Rat Cardiac Stem Cells

被引:27
作者
Di Felice, Valentina [1 ]
Ardizzone, Nella Maria [1 ]
De Luca, Angela [1 ]
Marciano, Vito [1 ]
Gammazza, Antonella Marino [1 ]
Macaluso, Filippo [1 ,2 ]
Manente, Lucrezia [3 ]
Cappello, Francesco [1 ,4 ]
De Luca, Antonio [3 ]
Zummo, Giovanni [1 ]
机构
[1] Univ Palermo, Dept Expt Med, Human Anat Sect, I-90127 Palermo, Italy
[2] Univ Stellenbosch, Dept Physiol Sci, ZA-7600 Stellenbosch, South Africa
[3] Univ Naples 2, Dept Med & Publ Hlth, Human Anat Sect, Naples, Italy
[4] IEMEST, I-90139 Palermo, Italy
关键词
THERAPY POSITION STATEMENT; MUSCLE DIFFERENTIATION; INTERNATIONAL-SOCIETY; PROGENITOR CELLS; HEART; CARDIOMYOCYTES; REGENERATION; DEATH; TRANSPLANTATION; MULTIPOTENT;
D O I
10.1002/jcp.21912
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
In the last few years, a major goal of cardiac research has been to drive stem cell differentiation to replace damaged myocardium. Several research groups have attempted to differentiate potential cardiac stem cells (CSCs) using bi- or three-dimensional systems supplemented with growth factors or molecules acting as differentiating substances. We hypothesize that these systems failed to induce a complete differentiation because they lacked an architectural space. In the present study, we isolated a pool of small proliferating and fibroblast-like cells from adult rat myocardium. The phenotype of these cells was assessed and the characterized cells were cultured in a collagen I/OPLA scaffold with horse serum to obtain fine myocardial differentiation. C-Kit(POS)/Sca-1(POS) CSCs fully differentiated in vitro when an environment more similar to the CSC niche was created. These experiments demonstrated an important model for the study of the biology of CSCs and the biochemical pathways that lead to myocardial differentiation. The results pave the way for a new surgical approach. J. Cell. Physiol. 221: 729-739, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:729 / 739
页数:11
相关论文
共 40 条
[1]
Life and death of cardiac stem cells - A paradigm shift in cardiac biology [J].
Anversa, P ;
Kajstura, J ;
Leri, A ;
Bolli, R .
CIRCULATION, 2006, 113 (11) :1451-1463
[2]
Stem cells in adult skeletal muscle [J].
Asakura, A .
TRENDS IN CARDIOVASCULAR MEDICINE, 2003, 13 (03) :123-128
[3]
Adult cardiac stem cells are multipotent and support myocardial regeneration [J].
Beltrami, AP ;
Barlucchi, L ;
Torella, D ;
Baker, M ;
Limana, F ;
Chimenti, S ;
Kasahara, H ;
Rota, M ;
Musso, E ;
Urbanek, K ;
Leri, A ;
Kajstura, J ;
Nadal-Ginard, B ;
Anversa, P .
CELL, 2003, 114 (06) :763-776
[4]
Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart [J].
Cai, CL ;
Liang, XQ ;
Shi, YQ ;
Chu, PH ;
Pfaff, SL ;
Chen, J ;
Evans, S .
DEVELOPMENTAL CELL, 2003, 5 (06) :877-889
[5]
CARRASCO FH, 1981, BLOOD VESSELS, V18, P296
[6]
TISSUE ENGINEERING BY CELL TRANSPLANTATION USING DEGRADABLE POLYMER SUBSTRATES [J].
CIMA, LG ;
VACANTI, JP ;
VACANTI, C ;
INGBER, D ;
MOONEY, D ;
LANGER, R .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1991, 113 (02) :143-151
[7]
Pkn is a novel partner of cyclin T2a in muscle differentiation [J].
Cottone, G ;
Baldi, A ;
Palescandolo, E ;
Manente, L ;
Penta, R ;
Paggi, MG ;
De Luca, A .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 207 (01) :232-237
[8]
Cardiac stem cells delivered intravascularly traverse the vessel barrier, regenerate infarcted myocardium, and improve cardiac function [J].
Dawn, B ;
Stein, AB ;
Urbanek, K ;
Rota, M ;
Whang, B ;
Rastaldo, R ;
Torella, D ;
Tang, XL ;
Rezazadeh, A ;
Kajstura, J ;
Leri, A ;
Hunt, G ;
Varma, J ;
Prabhu, SD ;
Anversa, P ;
Bolli, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (10) :3766-3771
[9]
De Falco M, 2006, EUR J HISTOCHEM, V50, P19
[10]
HSP90 and eNOS partially co-localize and change cellular localization in relation to different ECM components in 2D and 3D cultures of adult rat cardiomyocytes [J].
Di Felice, Valentina ;
Cappello, Francesco ;
Montalbano, Antonella ;
Ardizzone, Nella Maria ;
De Luca, Angela ;
Macaluso, Filippo ;
Amelio, Daniela ;
Cerra, Maria Carmela ;
Zummo, Giovanni .
BIOLOGY OF THE CELL, 2007, 99 (12) :689-699