TGF-β1 diminishes collagen production during long-term cyclic stretching of engineered connective tissue: Implication of decreased ERK signaling

被引:34
作者
Syedain, Zeeshan H. [1 ,2 ]
Tranquillo, Robert T. [1 ,2 ]
机构
[1] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
关键词
Tissue engineering; Tissue growth and remodeling; TGF-beta; ERK; p38; Cyclic stretching; Collagen deposition; GROWTH-FACTOR-BETA; IN-VITRO; GENE-EXPRESSION; FIBRIN; TRANSCRIPTION; FIBROBLASTS; ACTIVATION; ELASTIN; STIMULATION; CONSTRUCTS;
D O I
10.1016/j.jbiomech.2010.12.007
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Cyclic stretching and growth factors like TGF-beta have been used to enhance extracellular matrix (ECM) production by cells in engineered tissue to achieve requisite mechanical properties. In this study, the effects of TGF-beta 1 were evaluated during long-term cyclic stretching of fibrin-based tubular constructs seeded with neonatal human dermal fibroblasts. Samples were evaluated at 2, 5, and 7 weeks for tensile mechanical properties and ECM deposition. At 2 weeks, +TGF-beta 1 samples had 101% higher collagen concentration but no difference in ultimate tensile strength (UTS) or modulus compared to -TGF-beta 1 samples. However, at weeks 5 and 7, -TGF-beta 1 samples had higher UTS/modulus and collagen concentration, but lower elastin concentration compared to +TGF-beta 1 samples. The collagen was better organized in -TGF-beta 1 samples based on picrosirius red staining. Western blot analysis at weeks 5 and 7 showed increased phosphorylation of ERK in -TGF-beta 1 samples, which correlated with higher collagen deposition. The TGF-beta 1 effects were further evaluated by western blot for alpha SMA and SMAD2/3 expression, which were 16-fold and 10-fold higher in +TGF-beta 1 samples, respectively. The role of TGF-beta 1 activated p38 in inhibiting phosphorylation of ERK was evaluated by treating samples with SB203580, an inhibitor of p38 activation. SB203580-treated cells showed increased phosphorylation of ERK after 1 hour of stretching and increased collagen production after 1 week of stretching, demonstrating an inhibitory role of activated p38 via TGF-beta 1 signaling during cyclic stretching. One advantage of TGF-beta 1 treatment was the 4-fold higher elastin deposition in samples at 7 weeks. Further cyclic stretching experiments were thus conducted with constructs cultured for 5 weeks without TGF-beta 1 to obtain improved tensile properties followed by TGF-beta 1 supplementation for 2 weeks to obtain increased elastin content, which correlated with a reduction in loss of pre-stress during preconditioning for tensile testing, indicating functional elastin. This study shows that a sequential stimulus approach - cyclic stretching with delayed TGF-beta 1 supplementation - can be used to engineer tissue with desirable tensile and elastic properties. (c) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:848 / 855
页数:8
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