Engineered spatial patterns of FGF-2 immobilized on fibrin direct cell organization

被引:113
作者
Campbell, PG
Miller, ED
Fisher, GW
Walker, LM
Weiss, LE
机构
[1] Carnegie Mellon Univ, Inst Complex Engn Syst, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Biomed Engn, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Mol Biosensor & Imaging Ctr, Pittsburgh, PA 15213 USA
[4] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
[5] Carnegie Mellon Univ, Inst Robot, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
tissue engineering inkjet technology; solid freeform fabrication; growth factor; printing technology; biological patterning;
D O I
10.1016/j.biomaterials.2005.04.032
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The purpose of this study was to initiate the exploration of cell behavioral responses to inkjet printed spatial patterns of hormones biologically immobilized on biomimetic Substrates. This approach was investigated using the example of preosteoblastic cell response in vitro to fibroblast growth factor-2 (FGF-2) printed oil fibrin films. Concentration modulated patterns of FGF-2. including continuous concentration gradients. were created by overprinting dilute FGF-2 bioinks with it custom inkjet printer. The immobilized, FGF-2 was biologically active and the printed patterns Persisted up to 10 days under Cell Culture Conditions. Cell numbers increased in register to printed patterns from in initial random uniform cell distribution across the patterned and nonpatterned fibrin substrate. Patterned immobilized FGF-2, not cell attachment directed cell organization because the librin substrate was homogeneous. The capability to engineer arbitrary and persistent hormone patterns is relevant to basic studies across various fields including developmental biology and tissue regeneration. Furthermore. since this hormone inkjet printing methodology is extensible to create complex three-dimensional structures. this methodology has potential it, create therapies for tissue engineering using spatial patterned delivery of exogenous hormones. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6762 / 6770
页数:9
相关论文
共 41 条
[1]   Temporal and spatial regulation of VEGF-A controls vascular patterning in the embryonic lung [J].
Akeson, AL ;
Greenberg, JM ;
Cameron, JE ;
Thompson, FY ;
Brooks, SK ;
Wiginton, D ;
Whitsett, JA .
DEVELOPMENTAL BIOLOGY, 2003, 264 (02) :443-455
[2]   Functions of cell surface heparan sulfate proteoglycans [J].
Bernfield, M ;
Götte, M ;
Park, PW ;
Reizes, O ;
Fitzgerald, ML ;
Lincecum, J ;
Zako, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :729-777
[3]   Biological roles of fibroblast growth factor-2 [J].
Bikfalvi, A ;
Klein, S ;
Pintucci, G ;
Rifkin, DB .
ENDOCRINE REVIEWS, 1997, 18 (01) :26-45
[5]   Insulin-like growth factor-binding protein-3 binds fibrinogen and fibrin [J].
Campbell, PG ;
Durham, SK ;
Hayes, JD ;
Suwanichkul, A ;
Powell, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (42) :30215-30221
[6]   Gradient micropattern immobilization of EGF to investigate the effect of artificial juxtacrine stimulation [J].
Chen, GP ;
Ito, YY .
BIOMATERIALS, 2001, 22 (18) :2453-2457
[7]  
Clark RAF, 2001, ANN NY ACAD SCI, V936, P355
[8]   Positive microcontact printing [J].
Delamarche, E ;
Geissler, M ;
Wolf, H ;
Michel, B .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (15) :3834-3835
[9]   THEORY OF BIOLOGICAL PATTERN FORMATION [J].
GIERER, A ;
MEINHARDT, H .
KYBERNETIK, 1972, 12 (01) :30-39
[10]   Morphogen gradient interpretation [J].
Gurdon, JB ;
Bourillot, PY .
NATURE, 2001, 413 (6858) :797-803