Engineering microenvironment for expansion of sensitive anchorage-dependent mammalian cells

被引:8
作者
Chia, SM
Lin, PC
Quek, CH
Yin, C
Mao, HQ
Leong, KW
Xu, X
Goh, CH
Ng, ML
Yu, H [1 ]
机构
[1] Natl Univ Singapore, Fac Med, Singapore 117548, Singapore
[2] ASTAR, Inst Mat Res & Engn, Singapore, Singapore
[3] Johns Hopkins Singapore Biomed Ctr, Singapore, Singapore
[4] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD USA
[5] ASTAR, Inst Bioengn & Nanotechnol, Singapore, Singapore
基金
英国医学研究理事会;
关键词
microencapsulation; cell expansion; anchorage-dependent mammalian cells; non-disruptive harvesting; tissue engineering; stem cell research;
D O I
10.1016/j.jbiotec.2005.05.012
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
Tissue engineering involves ex. vivo seeding of anchorage-dependent mammalian cells onto scaffolds, or transplanting cells in vivo. The cell expansion currently requires repeated cell detachment from solid substrata by enzymatic, chemical or mechanical means. The report here presents a high yield three-dimensional culture and harvest system circumventing the conventional detachment requirements. Cells mixed with dilute cationic collagen were microencapsulated within an ultra-thin shell of synthetic polymers. The cationic collagen could rapidly form a conformal layer of collagen fibers around cells to support cell proliferation and functions. The collagen could be readily removed from cells with a buffer rinse after harvesting from the fragile microcapsules. The cells harvested from this system demonstrate improved attachment, morphology and functions over conventionally cultured cells, upon binding to ligand-conjugated polymer surfaces. The harvested cells can be re-encapsulated and allowed to proliferate again, or used immediately in applications. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:434 / 447
页数:14
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