Thomopoulos Stavros, Fomovsky Gregory M, Holmes Jeffrey W
Department of Orthopaedic Surgery, Washington University School of Medicine, 1 Barnes-Jewish Hospital Plaza, Suite 11300, Campus Box 8233, St, Louis, MO 63110, USA.
J Biomech Eng. 2005 Oct;127(5):742-50. doi: 10.1115/1.1992525.
An in vitro model system was developed to study structure-function relationships and the development of structural and mechanical anisotropy in collagenous tissues. Fibroblast-populated collagen gels were constrained either biaxially or uniaxially. Gel remodeling, biaxial mechanical properties, and collagen orientation were determined after 72 h of culture. Collagen gels contracted spontaneously in the unconstrained direction, uniaxial mechanical constraints produced structural anisotropy, and this structural anisotropy was associated with mechanical anisotropy. Cardiac and tendon fibroblasts were compared to test the hypothesis that tendon fibroblasts should generate greater anisotropy in vitro. However, no differences were seen in either structure or mechanics of collagen gels populated with these two cell types, or between fibroblast populated gels and acellular gels. This study demonstrates our ability to control and measure the development of structural and mechanical anisotropy due to imposed mechanical constraints in a fibroblast-populated collagen gel model system. While imposed constraints were required for the development of anisotropy in this system, active remodeling of the gel by fibroblasts was not. This model system will provide a basis for investigating structure-function relationships in engineered constructs and for studying mechanisms underlying the development of anisotropy in collagenous tissues.
为了研究胶原组织的结构-功能关系以及结构和力学各向异性的发展,开发了一种体外模型系统。接种成纤维细胞的胶原凝胶受到双轴或单轴约束。培养72小时后,测定凝胶重塑、双轴力学性能和胶原取向。胶原凝胶在无约束方向自发收缩,单轴力学约束产生结构各向异性,且这种结构各向异性与力学各向异性相关。比较心脏和肌腱成纤维细胞,以检验肌腱成纤维细胞在体外应产生更大各向异性的假设。然而,接种这两种细胞类型的胶原凝胶在结构或力学方面均未观察到差异,接种成纤维细胞的凝胶与无细胞凝胶之间也未观察到差异。本研究证明了我们在接种成纤维细胞的胶原凝胶模型系统中,通过施加力学约束来控制和测量结构和力学各向异性发展的能力。虽然在该系统中各向异性的发展需要施加约束,但成纤维细胞对凝胶的主动重塑并非必需。该模型系统将为研究工程构建物中的结构-功能关系以及胶原组织中各向异性发展的潜在机制提供基础。