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
[1]
Migration and differentiation of neural precursor cells can be directed by microglia [J].
Aarum, J ;
Sandberg, K ;
Haeberlein, SLB ;
Persson, MAA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (26) :15983-15988
[2]
DEVELOPMENT OF INTRACEREBRAL DOPAMINERGIC GRAFTS - A COMBINED IMMUNOHISTOCHEMICAL AND AUTORADIOGRAPHIC STUDY OF ITS TIME COURSE AND ENVIRONMENTAL-INFLUENCES [J].
ABROUS, N ;
GUY, J ;
VIGNY, A ;
CALAS, A ;
LEMOAL, M ;
HERMAN, JP .
JOURNAL OF COMPARATIVE NEUROLOGY, 1988, 273 (01) :26-41
[3]
Tissue-engineered osteochondral constructs in the shape of an articular condyle [J].
Alhadlaq, A ;
Mao, JJ .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2005, 87A (05) :936-944
[4]
Adult stem cell driven genesis of human-shaped articular condyle [J].
Alhadlaq, A ;
Elisseeff, JH ;
Hong, L ;
Williams, CG ;
Caplan, AI ;
Sharma, B ;
Kopher, RA ;
Tomkoria, S ;
Lennon, DP ;
Lopez, A ;
Mao, JJ .
ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (07) :911-923
[5]
Cell differentiation by mechanical stress [J].
Altman, GH ;
Horan, RL ;
Martin, I ;
Farhadi, J ;
Stark, PRH ;
Volloch, V ;
Richmond, JC ;
Vunjak-Novakovic, G ;
Kaplan, DL .
FASEB JOURNAL, 2001, 15 (14) :270-+
[7]
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
[8]
NEUROTROPHIN-4 SELECTIVELY PROMOTES SURVIVAL OF STRIATAL NEURONS IN ORGANOTYPIC SLICE CULTURE [J].
ARDELT, AA ;
FLARIS, NA ;
ROTH, KA .
BRAIN RESEARCH, 1994, 647 (02) :340-344
[9]
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
[10]
Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228