Differentiation of Stem Cells: Strategies for Modifying Surface Biomaterials

被引:38
作者
Fu, Ru-Huei [1 ,2 ]
Wang, Yu-Chi [3 ]
Liu, Shih-Ping [1 ,4 ]
Huang, Chin-Mao [1 ]
Kang, Yun-Han [1 ]
Tsai, Chang-Hai [5 ,6 ]
Shyu, Woei-Cherng [1 ,2 ]
Lin, Shinn-Zong [1 ,2 ,7 ]
机构
[1] China Med Univ Hosp, Ctr Neuropsychiat, Taichung, Taiwan
[2] China Med Univ, Grad Inst Immunol, Taichung, Taiwan
[3] Biotechplex Corp, San Diego, CA USA
[4] China Med Univ, Grad Inst Basic Med Sci, Taichung, Taiwan
[5] China Med Univ Hosp, Dept Pediat, Taichung, Taiwan
[6] Asia Univ, Dept Healthcare Adm, Taichung, Taiwan
[7] China Med Univ Beigang Hosp, Yunlin, Taiwan
关键词
Stem cells; Biomaterials; Tissue engineering; Extracellular matrix (ECM); MESENCHYMAL STROMAL CELLS; CHONDROGENIC DIFFERENTIATION; GENE-EXPRESSION; SELF-RENEWAL; CORD-BLOOD; SCAFFOLD; GROWTH; ATTACHMENT; PROLIFERATION; HYDROGEL;
D O I
10.3727/096368910X532756
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Stem cells are a natural choice for cellular therapy because of their potential to differentiate into a variety of lineages, their capacity for self-renewal in the repair of damaged organs and tissues in vivo, and their ability to generate tissue constructs in vitro. Determining how to efficiently drive stem cell differentiation to a lineage of choice is critical for the success of cellular therapeutics. Many factors are involved in this process, the extracellular microenvironment playing a significant role in controlling cellular behavior. In recent years, researchers have focused on identifying a variety of biomaterials to provide a microenvironment that is conducive to stem cell growth and differentiation and that ultimately mimics the in vivo situation. Appropriate biomaterials support the cellular attachment, proliferation, and lineage-specific differentiation of stem cells. Tissue engineering approaches have been used to incorporate growth factors and morphogenetic factors-factors known to induce lineage commitment of stem cells-into cultures with scaffolding materials, including synthetic and naturally derived biomaterials. This review focuses on various strategies that have been used in stem cell expansion and examines modifications of natural and synthetic materials, as well as various culture conditions, for the maintenance and lineage-specific differentiation of embryonic and adult stem cells.
引用
收藏
页码:37 / 47
页数:11
相关论文
共 103 条
[1]  
Agrawal CM, 2001, J BIOMED MATER RES, V55, P141, DOI 10.1002/1097-4636(200105)55:2<141::AID-JBM1000>3.3.CO
[2]  
2-A
[3]   Modulation of the Keratinocyte-Fibroblast Paracrine Relationship with Gelatin-Based Semi-interpenetrating Networks Containing Bioactive Factors for Wound Repair [J].
Bader, Rebecca A. ;
Kao, Andweiyuan John .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2009, 20 (7-8) :1005-1030
[4]   Identification of stem cells in small intestine and colon by marker gene Lgr5 [J].
Barker, Nick ;
van Es, Johan H. ;
Kuipers, Jeroen ;
Kujala, Pekka ;
van den Born, Maaike ;
Cozijnsen, Miranda ;
Haegebarth, Andrea ;
Korving, Jeroen ;
Begthel, Harry ;
Peters, Peter J. ;
Clevers, Hans .
NATURE, 2007, 449 (7165) :1003-U1
[5]   Improved attachment of mesenchymal stem cells on super-hydrophobic TiO2 nanotubes [J].
Bauer, Sebastian ;
Park, Jung ;
von der Mark, Klaus ;
Schmuki, Patrik .
ACTA BIOMATERIALIA, 2008, 4 (05) :1576-1582
[6]   Ex vivo enrichment of mesenchymal cell progenitors by fibroblast growth factor 2 [J].
Bianchi, G ;
Banfi, A ;
Mastrogiacomo, M ;
Notaro, R ;
Luzzatto, L ;
Cancedda, R ;
Quarto, R .
EXPERIMENTAL CELL RESEARCH, 2003, 287 (01) :98-105
[7]   COVALENT ATTACHMENT OF AN ARG-GLY-ASP SEQUENCE PEPTIDE TO DERIVATIZABLE POLYACRYLAMIDE SURFACES - SUPPORT OF FIBROBLAST ADHESION AND LONG-TERM GROWTH [J].
BRANDLEY, BK ;
SCHNAAR, RL .
ANALYTICAL BIOCHEMISTRY, 1988, 172 (01) :270-278
[8]  
Brun P, 1999, J BIOMED MATER RES, V46, P337, DOI 10.1002/(SICI)1097-4636(19990905)46:3<337::AID-JBM5>3.3.CO
[9]  
2-H
[10]   Umbilical cord blood transplantation after nonmyeloablative conditioning: impact on transplantation outcomes in 110 adults with hematologic disease [J].
Brunstein, Claudio G. ;
Barker, Juliet N. ;
Weisdorf, Daniel J. ;
DeFor, Todd E. ;
Miller, Jeffrey S. ;
Blazar, Bruce R. ;
McGlave, Philip B. ;
Wagner, John E. .
BLOOD, 2007, 110 (08) :3064-3070