Molecular signaling in bioengineered tissue microenvironments

被引:65
作者
Bottaro, DP
Liebmann-Vinson, A
Heidaran, MA
机构
[1] EntreMed Inc, Rockville, MD 20850 USA
[2] BD Technol Inc, Res Triangle Pk, NC 27709 USA
来源
REPARATIVE MEDICINE: GROWING TISSUES AND ORGANS | 2002年 / 961卷
关键词
molecular signaling; biomimetic microenvironments; tissue scaffolds;
D O I
10.1111/j.1749-6632.2002.tb03068.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Biological tissues and organs consist of specialized living cells arrayed within a complex structural and functional framework known generally as the extracellular matrix (ECM). The great diversity observed in the morphology and composition of the ECM contributes enormously to the properties and function of each organ and tissue. For example, the ECM contributes to the rigidity and tensile strength of bone, the resilience of cartilage, the flexibility and hydrostatic strength of blood vessels, and the elasticity of skin. The ECM is also important during growth, development, and wound repair: its own dynamic composition acts as a reservoir for soluble signaling molecules and mediates signals from other sources to migrating, proliferating, and differentiating cells. Artificial three-dimensional substitutes for ECM, called tissue scaffolds, may consist of natural or synthetic polymers or a combination of both. Scaffolds have been used successfully alone and in combination with cells and soluble factors to induce tissue formation or promote tissue repair. Appropriate numbers of properly functioning living cells are central to many tissue-engineering strategies, and significant efforts have been made to identify and propagate pluripotent stem cells and lineage-restricted progenitor cells. The study of these and other living cells in artificial microenvironments, in turn, has led to the identifcation of signaling events important for their controlled proliferation, proper differentiation, and optimal function.
引用
收藏
页码:143 / 153
页数:11
相关论文
共 69 条
[1]   Biodegradable PLA-PGA polymers for tissue engineering in orthopaedics [J].
Agrawal, CM ;
Athanasiou, KA ;
Heckman, JD .
POROUS MATERIALS FOR TISSUE ENGINEERING, 1997, 250 :115-128
[2]  
[Anonymous], PRINCIPLES TISSUE EN
[3]   Tissue engineered cartilage [J].
Ashiku, SK ;
Randolph, MA ;
Vacanti, CA .
POROUS MATERIALS FOR TISSUE ENGINEERING, 1997, 250 :129-150
[4]   Anchorage-dependent cell cycle progression [J].
Assoian, RK .
JOURNAL OF CELL BIOLOGY, 1997, 136 (01) :1-4
[5]   NERVE-FIBER GROWTH ON DEFINED HYDROGEL SUBSTRATES [J].
CARBONETTO, ST ;
GRUVER, MM ;
TURNER, DC .
SCIENCE, 1982, 216 (4548) :897-899
[6]   Fabrication of PLGA-collagen hybrid sponge [J].
Chen, GP ;
Ushida, T ;
Tateishi, T .
CHEMISTRY LETTERS, 1999, (07) :561-562
[7]  
Chen GP, 2000, ADV MATER, V12, P455, DOI 10.1002/(SICI)1521-4095(200003)12:6<455::AID-ADMA455>3.0.CO
[8]  
2-C
[9]   Mechanotransduction in response to shear stress - Roles of receptor tyrosine kinases, integrins, and Shc [J].
Chen, KD ;
Li, YS ;
Kim, M ;
Li, S ;
Yuan, S ;
Chien, S ;
Shyy, JYJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (26) :18393-18400
[10]   Retinoblastoma protein positively regulates terminal adipocyte differentiation through direct interaction with C/EBPs [J].
Chen, PL ;
Riley, DJ ;
Chen, YM ;
Lee, WH .
GENES & DEVELOPMENT, 1996, 10 (21) :2794-2804