Amos Jennifer R, Li Shigeng, Yost Michael, Ploehn Harry, Potts Jay D
Department of Chemical Engineering, University of South Carolina, Columbia, SC 29208, USA.
Biorheology. 2009;46(6):439-50. doi: 10.3233/BIR-2009-0553.
In this work, we studied the effects of tensile strain on limb bud mesenchymal cells (MSC) cultured on a collagen type I tubular scaffold. A novel bioreactor was designed to culture the cells while subjecting the tubular scaffold to tensile stress and strain. Control samples included unseeded and MSC-seeded tubes cultured for 2 weeks under unloaded, no-strain conditions, and unseeded tubes subjected to prolonged tensile stress and strain. Mechanical properties of tube specimens were measured under oscillatory compressive stress. Following mechanical testing, scaffolds were fixed for immunohistochemistry or frozen for mRNA extraction. The storage modulii of both seeded/unstrained and seeded/strained tubes were significantly less than that of unseeded tubes, suggesting that MSC disrupted the structure and elasticity of the tubes' collagen type I. At a frequency of 1.0 Hz, the loss tangent of seeded/strained tubes was more than 2.5 times greater than that of seeded/unstrained tubes, and almost 6 times greater than that of unseeded tubes. Confocal microscopy and qRT-PCR results demonstrated that collagen type II and aggrecan expression was upregulated in the seeded/strained tubes. The images also show, for the first time, that culture under tensile strain induces MSC to remodel the collagen type I tube with collagen type II and aggrecan expression into fibrils dispersed throughout the matrix. The seeded/unstrained tubes manifested less collagen type II with a more random expression pattern. Compared to seeded/unstrained tubes, qRT-PCR for collagen type II in the seeded/strained tubes showed a 4-fold increase in the message for collagen type II and a 13-fold increase in the message for aggrecan. These results demonstrate that MSC cultured for at least some period under tensile strain are able to remodel collagen type I scaffolds to produce a more viscous construct having many of the mechanical and biological features of engineered cartilage.
在本研究中,我们探究了拉伸应变对在I型胶原管状支架上培养的肢芽间充质细胞(MSC)的影响。我们设计了一种新型生物反应器,用于在对管状支架施加拉伸应力和应变的同时培养细胞。对照样本包括在无负载、无应变条件下培养2周的未接种细胞和接种了MSC的管子,以及经受长时间拉伸应力和应变的未接种细胞的管子。在振荡压缩应力下测量管样本的力学性能。力学测试后,将支架固定用于免疫组织化学分析或冷冻用于mRNA提取。接种细胞/未受应变的管子和接种细胞/受应变的管子的储能模量均显著低于未接种细胞的管子,这表明MSC破坏了管子I型胶原的结构和弹性。在1.0 Hz的频率下,接种细胞/受应变的管子的损耗角正切比接种细胞/未受应变的管子大2.5倍以上,几乎比未接种细胞的管子大6倍。共聚焦显微镜和定量逆转录聚合酶链反应(qRT-PCR)结果表明,接种细胞/受应变的管子中II型胶原和聚集蛋白聚糖的表达上调。图像还首次显示,在拉伸应变下培养可诱导MSC将表达II型胶原和聚集蛋白聚糖的I型胶原管重塑为分散在整个基质中的纤维。接种细胞/未受应变的管子中II型胶原较少,表达模式更随机。与接种细胞/未受应变的管子相比,接种细胞/受应变的管子中II型胶原的qRT-PCR显示II型胶原信息增加了4倍,聚集蛋白聚糖信息增加了13倍。这些结果表明,在拉伸应变下培养至少一段时间的MSC能够重塑I型胶原支架,以产生一种具有工程软骨许多力学和生物学特性的更具粘性的构建体。