Progress and Prospects for Stem Cell Engineering

被引:25
作者
Ashton, Randolph S. [1 ]
Keung, Albert J. [1 ]
Peltier, Joseph [1 ]
Schaffer, David V. [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA
来源
ANNUAL REVIEW OF CHEMICAL AND BIOMOLECULAR ENGINEERING, VOL 2 | 2011年 / 2卷
关键词
high-throughput; microenvironment; systems and computational biology; bioreactors; TERM SELF-RENEWAL; EMBRYOID BODIES; GENE-EXPRESSION; CARDIOMYOCYTE DIFFERENTIATION; INTERACTION NETWORK; SUSPENSION-CULTURE; MATHEMATICAL-MODEL; MEDIATED CONTROL; STRUCTURAL BASIS; SYSTEMS BIOLOGY;
D O I
10.1146/annurev-chembioeng-061010-114105
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Stem cells offer tremendous biomedical potential owing to their abilities to self-renew and differentiate into cell types of multiple adult tissues. Researchers and engineers have increasingly developed novel discovery technologies, theoretical approaches, and cell culture systems to investigate microenvironmental cues and cellular signaling events that control stern cell fate. Many of these technologies facilitate high-throughput investigation of microenvironmental signals and the intracellular signaling networks and machinery processing those signals into cell fate decisions. As our aggregate empirical knowledge of stem cell regulation grows, theoretical modeling with systems and computational biology methods has and will continue to be important for developing our ability to analyze and extract important conceptual features of stem cell regulation from complex data. Based on this body of knowledge, stem cell engineers will continue to develop technologies that predictably control stem cell fate with the ultimate goal of being able to accurately and economically scale up these systems for clinical-grade production of stem cell therapeutics.
引用
收藏
页码:479 / 502
页数:24
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