Environmental cues to guide stem cell fate decision for tissue engineering applications

被引:64
作者
Alsberg, Eben
von Recum, Horst A.
Mahoney, Melissa J.
机构
[1] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[2] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
关键词
biomaterials; endothelial precursor cells; mesenchymal stem cells; neural stem cells; regenerative medicine; tissue engineering;
D O I
10.1517/14712598.6.9.847
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 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The human body contains a variety of stem cells capable of both repeated self-renewal and production of specialised, differentiated progeny. Critical to the implementation of these cells in tissue engineering strategies is a thorough understanding of which external signals in the stem cell microenvironment provide cues to control their fate decision in terms of proliferation or differentiation into a desired, specific phenotype. These signals must then be incorporated into tissue regeneration approaches for regulated exposure to stem cells. The precise spatial and temporal presentation of factors directing stem cell behaviour is extremely important during embryogenesis, development and natural healing events, and it is possible that this level of control will be vital to the success of many regenerative therapies. This review covers existing tissue engineering approaches to guide the differentiation of three disparate stem cell populations: mesenchymal, neural and endothelial. These progenitor cells will be of central importance in many future connective, neural and vascular tissue regeneration technologies.
引用
收藏
页码:847 / 866
页数:20
相关论文
共 248 条
[11]
VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[12]
Shear-stress preconditioning and tissue-engineering-based paradigms for generating arterial substitutes [J].
Baguneid, M ;
Murray, D ;
Salacinski, HJ ;
Fuller, B ;
Hamilton, G ;
Walker, M ;
Seifalian, AM .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2004, 39 (02) :151-157
[13]
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
[14]
SUCCESS RATE OF PRIMARY HUMAN-ENDOTHELIAL CELL-CULTURE FROM UMBILICAL CORDS IS INFLUENCED BY MATERNAL AND FETAL FACTORS AND INTERVAL FROM DELIVERY [J].
BALCONI, G ;
PIETRA, A ;
BUSACCA, M ;
DEGAETANO, G ;
DEJANA, E .
IN VITRO-JOURNAL OF THE TISSUE CULTURE ASSOCIATION, 1983, 19 (11) :807-810
[15]
Agarose gel stiffness determines rate of DRG neurite extension in 3D cultures [J].
Balgude, AP ;
Yu, X ;
Szymanski, A ;
Bellamkonda, RV .
BIOMATERIALS, 2001, 22 (10) :1077-1084
[16]
The time course of loss of dopaminergic neurons and the gliotic reaction surrounding grafts of embryonic mesencephalon to the striatum [J].
Barker, RA ;
Dunnett, SB ;
Faissner, A ;
Fawcett, JW .
EXPERIMENTAL NEUROLOGY, 1996, 141 (01) :79-93
[17]
Mesenchymal stem cells: clinical applications and biological characterization [J].
Barry, FP ;
Murphy, JM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2004, 36 (04) :568-584
[18]
Expression and secretion of vascular endothelial growth factor-A by cytokine-stimulated hematopoietic progenitor cells:: Possible role in the hematopoietic microenvironment [J].
Bautz, F ;
Rafii, S ;
Kanz, L ;
Möhle, R .
EXPERIMENTAL HEMATOLOGY, 2000, 28 (06) :700-706
[19]
LAMININ OLIGOPEPTIDE DERIVATIZED AGAROSE GELS ALLOW 3-DIMENSIONAL NEURITE EXTENSION IN-VITRO [J].
BELLAMKONDA, R ;
RANIERI, JP ;
AEBISCHER, P .
JOURNAL OF NEUROSCIENCE RESEARCH, 1995, 41 (04) :501-509
[20]
Adenoviral brain-derived neurotrophic factor induces both neostriatal and olfactory neuronal recruitment from endogenous progenitor cells in the adult forebrain [J].
Benraiss, A ;
Chmielnicki, E ;
Lerner, K ;
Roh, D ;
Goldman, SA .
JOURNAL OF NEUROSCIENCE, 2001, 21 (17) :6718-6731