The effect of matrix composition of 3D constructs on embryonic stem cell differentiation

被引:184
作者
Battista, S
Guarnieri, D
Borselli, C
Zeppetelli, S
Borzacchiello, A
Mayol, L
Gerbasio, D
Keene, DR
Ambrosio, L
Netti, PA [1 ]
机构
[1] CNR, Inst Biomed & Composites Mat, I-80125 Naples, Italy
[2] Univ Naples Federico II, Dept Mat & Prod Engn, I-80125 Naples, Italy
[3] Univ Naples Federico II, CRIB, I-80125 Naples, Italy
[4] Shriners Hosp Children, Micro Imaging Ctr, Portland, OR 97239 USA
关键词
stem cell; collagen; fibronectin; laminin;
D O I
10.1016/j.biomaterials.2005.04.003
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The use of embryonic stem (ES) cells as unlimited cell source in tissue engineering has ignited the hope of regenerating any kind of tissue in vitro. However, the role of the material in control and guidance of their development and commitment into complex and viable three-dimensional (3D) tissues is still poorly understood. In this work, we investigate the role of material composition and structure on promoting ES cells growth and differentiation, by culturing mouse ES cell-derived embryoid bodies (EBs) in various semi-interpenetrating polymer networks (SIPNs), made of collagen, fibronectin (FN) and laminin (LM). We show that both composition and strength of the supportive matrix play an important role in EBs development. High collagen concentrations inhibit EBs cavitation and hence the following EBs differentiation, by inhibiting apoptosis. The presence of FN in 3D collagen constructs strongly stimulates endothelial cell differentiation and vascularization. Conversely, LM increases the ability of ES cells to differentiate into beating cardiomyocytes. Our data suggest that matrix composition has an important role in EBs development and that it is possible to influence stem cell differentiation toward preferential pattern, by modulating the physical and biochemical properties of the scaffold. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6194 / 6207
页数:14
相关论文
共 25 条
[1]   EMBRYONIC STEM-CELLS EXPRESS NEURONAL PROPERTIES IN-VITRO [J].
BAIN, G ;
KITCHENS, D ;
YAO, M ;
HUETTNER, JE ;
GOTTLIEB, DI .
DEVELOPMENTAL BIOLOGY, 1995, 168 (02) :342-357
[2]   Development of endothelial cell lines from embryonic stem cells - A tool for studying genetically manipulated endothelial cells in vitro [J].
Balconi, G ;
Spagnuolo, R ;
Dejana, E .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (06) :1443-1451
[3]   Loss of Hmga1 gene function affects embryonic stem cell lymphohematopoietic differentiation [J].
Battista, S ;
Pentimalli, F ;
Baldassarre, G ;
Fedele, M ;
Fidanza, V ;
Croce, CM ;
Fusco, A .
FASEB JOURNAL, 2003, 17 (09) :1496-+
[4]   APPROACHES TO STUDYING CELL-ADHESION MOLECULES IN ANGIOGENESIS [J].
BISCHOFF, J .
TRENDS IN CELL BIOLOGY, 1995, 5 (02) :69-74
[5]   SIGNALS FOR DEATH AND SURVIVAL - A 2-STEP MECHANISM FOR CAVITATION IN THE VERTEBRATE EMBRYO [J].
COUCOUVANIS, E ;
MARTIN, GR .
CELL, 1995, 83 (02) :279-287
[6]   Embryonic stem cell-derived adipogenesis [J].
Dani, C .
CELLS TISSUES ORGANS, 1999, 165 (3-4) :173-180
[7]  
DJABOUROV M, 1993, BIORHEOLOGY, V30, P191
[8]  
FERRY JD, 1970, VISCOELASTIC BEHAVIO, P33
[9]   Central roles of α5β1 integrin and fibronectin in vascular development in mouse embryos and embryoid bodies [J].
Francis, SE ;
Goh, KL ;
Hodivala-Dilke, K ;
Bader, BL ;
Stark, M ;
Davidson, D ;
Hynes, RO .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2002, 22 (06) :927-933
[10]  
GLUKHOVA MA, 1993, SEMIN CANCER BIOL, V4, P241