Wharton's Jelly Mesenchymal Stem Cell Response on Chitosan-graft-poly (ε -caprolactone) Copolymer for Myocardium Tissue Engineering

被引:13
作者
Chatzinikolaidou, Maria [1 ,3 ]
Kaliva, Maria [1 ,3 ]
Batsali, Aristea [2 ]
Pontikoglou, Charalampos [2 ]
Vamvakaki, Maria [1 ,3 ]
机构
[1] Univ Crete, Dept Mat Sci & Technol, Iraklion, Greece
[2] Univ Crete, Sch Med, Dept Hematol, Iraklion, Greece
[3] Fdn Res & Technol Hellas FORTH, Inst Elect Struct & Laser, Hellas, Greece
关键词
Wharton's jelly; chitosan grafted poly(epsilon-caprolactone); cell adhesion; viability; proliferation; myocardium regeneration; HUMAN UMBILICAL-CORD; HEART-FAILURE; IN-VITRO; INFARCTION; DIFFERENTIATION; TRANSPLANTATION; CARDIOMYOCYTES; SCAFFOLDS; HYDROGEL; OPTION;
D O I
10.2174/13816128113199990446
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Cell therapy and tissue engineering attract increasing attention as a potential approach for cardiac repair. Although a plethora of interesting concepts in the emerging field of cardiac stem cell-based tissue engineering are reported, there are still challenges that this field needs to overcome to achieve therapeutic translation into the clinical praxis. Engineering biomaterial scaffolds that facilitate stem cell engraftment, survival and homing are crucial for successful cellular cardiomyoplasty after myocardial infarction (MI). In this study we investigate for the first time the cellular response of Wharton's jelly (WJ) Mesenchymal Stem Cells (MSCs) on a copolymeric material comprising chitosan (CS) and poly(epsilon-caprolactone) (PCL). First we synthesize a copolymer consisting of poly(epsilon-caprolactone) grafted on a chemically modified chitosan-backbone (CS-g-PCL). Furthermore, we investigate the morphology, viability and proliferation of WJMSCs on material coatings and examine the cellular response from different donors. Our results show strong cell adhesion on the CS-g-PCL material surface from the first hours in culture, and a proliferation increase after 3 and 7 days. These findings support the potential use of our proposed cell-material combination in myocardium tissue engineering.
引用
收藏
页码:2030 / 2039
页数:10
相关论文
共 36 条
[1]
Breymann C, 2006, STEM CELL REV, V2, P87
[2]
A Facile Route for Regioselective Conjugation of Organo-Soluble Polymers onto Chitosan [J].
Cai, Guoqiang ;
Jiang, Hongliang ;
Tu, Kehua ;
Wang, Liqun ;
Zhu, Kangjie .
MACROMOLECULAR BIOSCIENCE, 2009, 9 (03) :256-261
[3]
Cardiomyoplasty: is it still a viable option in patients with end-stage heart failure? [J].
Chachques, Juan Carlos .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2009, 35 (02) :201-203
[4]
Stability of surface-enhanced ultrahydrophilic metals as a basis for bioactive rhBMP-2 surfaces [J].
Chatzinikolaidou, M ;
Zumbrink, T ;
Jennissen, HP .
MATERIALWISSENSCHAFT UND WERKSTOFFTECHNIK, 2003, 34 (12) :1106-1112
[5]
Endothelial differentiation of Wharton's jelly-derived mesenchymal stem cells in comparison with bone marrow-derived mesenchymal stem cells [J].
Chen, Ming-Yan ;
Lie, Pu-Chang ;
Li, Zhi-Ling ;
Wei, Xing .
EXPERIMENTAL HEMATOLOGY, 2009, 37 (05) :629-640
[6]
Biomaterials for the treatment of myocardial infarction [J].
Christman, Karen L. ;
Lee, Randall J. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 48 (05) :907-913
[7]
Conconi MT, 2006, INT J MOL MED, V18, P1089
[8]
Three-Dimensional Porous Scaffolds at the Crossroads of Tissue Engineering and Cell-Based Gene Therapy [J].
Coutu, Daniel L. ;
Yousefi, Azizeh-Mitra ;
Galipeau, Jacques .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 108 (03) :537-546
[9]
Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[10]
Cardiac tissue engineering [J].
Eschenhagen, T ;
Didié, M ;
Heubach, J ;
Ravens, U ;
Zimmermann, WH .
TRANSPLANT IMMUNOLOGY, 2002, 9 (2-4) :315-321