Investigating the Effect of Peptide Agonists on the Chondrogenic Differentiation of Human Mesenchymal Stem Cells using Design of Experiments

被引:20
|
作者
Renner, Julie N. [1 ]
Liu, Julie C. [1 ]
机构
[1] Purdue Univ, Sch Chem Engn, W Lafayette, IN 47907 USA
基金
美国国家科学基金会;
关键词
mesenchymal stem cell; cartilage tissue engineering; chondrogenesis; peptide and design of experiments; DEPENDENT GENE-EXPRESSION; GROWTH-FACTOR-I; BONE-MARROW; TRANSFORMING GROWTH-FACTOR-BETA-1; OSTEOGENIC DIFFERENTIATION; INSULIN; CARTILAGE; TISSUE; BMP-2; ACTIVATION;
D O I
10.1002/btpr.1808
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 ; 0836 ; 090102 ; 100705 ;
摘要
Human mesenchymal stem cells (MSCs) are attractive for use in cartilage tissue engineering. Cells are often seeded in a structural scaffold containing growth factors. Peptide mimics of full-length growth factors are a promising alternative because they are less expensive and easier to manufacture. We investigated four short peptides for their effect on the chondrogenesis of human MSCs. The peptides were originally designed to mimic bone morphogenetic protein-2 (BMP-2), transforming growth factor-beta 1 (TGF-1), and insulin, all of which have been shown to affect MSC chondrogenesis. Previous studies demonstrated that the peptides elicited bioactivity in other cell types, but the peptides have not been investigated for their effect on chondrogenesis in human MSCs. In a preliminary investigation, peptides were added to a pellet culture of human MSCs and assayed for their effect on glycosaminoglycan (GAG) production. These experiments determined peptide concentrations used in a full-factorial experiment to investigate any interactions. The experiment revealed the BMP peptide as a robust stimulant for GAG production. (c) 2013 American Institute of Chemical Engineers Biotechnol. Prog., 29:1550-1557, 2013
引用
收藏
页码:1550 / 1557
页数:8
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