Polymer-based Scaffold Designs For In Situ Vascular Tissue Engineering: Controlling Recruitment and Differentiation Behavior of Endothelial Colony Forming Cells

被引:39
作者
Fioretta, Emanuela S. [1 ]
Fledderus, Joost O. [2 ]
Burakowska-Meise, Ewelina A. [1 ]
Baaijens, Frank P. T.
Verhaar, Marianne C. [2 ]
Bouten, Carlijn V. C.
机构
[1] Eindhoven Univ Technol, Dept Biomed Engn, Biol Chem Lab, NL-5600 MB Eindhoven, Netherlands
[2] Univ Med Ctr Utrecht, Dept Hypertens & Nephrol, NL-3584 CX Utrecht, Netherlands
关键词
biomaterials; endothelial colony forming cells; in situ tissue engineering; peptides; transdifferentiation; WALL SHEAR-STRESS; SMOOTH-MUSCLE-CELLS; PROGENITOR CELLS; EXTRACELLULAR-MATRIX; GROWTH-FACTOR; BONE-MARROW; BIODEGRADABLE POLYMER; MECHANICAL-PROPERTIES; ELASTOMERIC SCAFFOLD; FIBER DIAMETER;
D O I
10.1002/mabi.201100315
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In situ vascular tissue engineering has been proposed as a promising approach to fulfill the need for small-diameter blood vessel substitutes. The approach comprises the use of a cell-free instructive scaffold to guide and control cell recruitment, differentiation, and tissue formation at the locus of implantation. Here we review the design parameters for such scaffolds, with special emphasis on differentiation of recruited ECFCs into the different lineages that constitute the vessel wall. Next to defining the target properties of the vessel, we concentrate on the target cell source, the ECFCs, and on the environmental control of the fate of these cells within the scaffold. The prospects of the approach are discussed in the light of current technical and biological hurdles.
引用
收藏
页码:577 / 590
页数:14
相关论文
共 131 条
[1]
SURFACE MODIFICATION OF POLYMERIC BIOMATERIALS WITH POLY(ETHYLENE OXIDE), ALBUMIN, AND HEPARIN FOR REDUCED THROMBOGENICITY [J].
AMIJI, M ;
PARK, K .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1993, 4 (03) :217-234
[2]
[Anonymous], 2009, FACT SHEET 317 CARD
[3]
Endothelial progenitor cell capture by stents coated with antibody against CD34 - The HEALING-FIM (healthy endothelial accelerated lining inhibits neointimal growth-first in man) registry [J].
Aoki, J ;
Serruys, PW ;
van Beusekom, H ;
Ong, ATL ;
McFadden, EP ;
Sianos, G ;
van der Giessen, WJ ;
Regar, E ;
de Feyter, PJ ;
Davis, HR ;
Rowland, S ;
Kutryk, MJB .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 45 (10) :1574-1579
[4]
Argento G., 2011, P ASME 2011 SUMM BIO
[5]
Heart valve development - Endothelial cell signaling and differentiation [J].
Armstrong, EJ ;
Bischoff, J .
CIRCULATION RESEARCH, 2004, 95 (05) :459-470
[6]
Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[7]
Induction of EPC homing on biofunctionalized vascular grafts for rapid in vivo self-endothelialization - A review of current strategies [J].
Avci-Adali, Meltem ;
Ziemer, Gerhard ;
Wendel, Hans P. .
BIOTECHNOLOGY ADVANCES, 2010, 28 (01) :119-129
[8]
Tailoring Fiber Diameter in Electrospun Poly(ε-Caprolactone) Scaffolds for Optimal Cellular Infiltration in Cardiovascular Tissue Engineering [J].
Balguid, Angelique ;
Mol, Anita ;
van Marion, Mieke H. ;
Bank, Ruud A. ;
Bouten, Carlijn V. C. ;
Baaijens, Frank P. T. .
TISSUE ENGINEERING PART A, 2009, 15 (02) :437-444
[9]
Amino alcohol-based degradable poly(ester amide) elastomers [J].
Bettinger, Christopher J. ;
Bruggeman, Joost P. ;
Borenstein, Jeffrey T. ;
Langer, Robert S. .
BIOMATERIALS, 2008, 29 (15) :2315-2325
[10]
Enhancement of in vitro capillary tube formation by substrate nanotopography [J].
Bettinger, Christopher J. ;
Zhang, Zhitong ;
Gerecht, Sharon ;
Borenstein, Jeffrey T. ;
Langer, Robert .
ADVANCED MATERIALS, 2008, 20 (01) :99-+