Kim B S, Mooney D J
Department of Chemical Engineering, University of Michigan, Ann Arbor 48109-2136, USA.
J Biomed Mater Res. 1998 Aug;41(2):322-32. doi: 10.1002/(sici)1097-4636(199808)41:2<322::aid-jbm18>3.0.co;2-m.
Nonwoven meshes of polyglycolic acid (PGA) fibers are attractive synthetic extracellular matrices (ECMs) for tissue engineering and have been used to engineer many types of tissues. However, these synthetic ECMs lack structural stability and often cannot maintain their original structure during tissue development. This makes it difficult to design an engineered tissue with a predefined configuration and dimensions. In this study, we investigated the ability of PGA fiber-based matrices bonded at their fiber crosspoints with a secondary polymer, poly-L-lactic acid (PLLA), to resist cellular contractile forces and maintain their predefined structure during the process of smooth muscle (SM) tissue development in vitro. Physically bonded PGA matrices exhibited a 10- to 35-fold increase in the compressive modulus over unbonded PGA matrices, depending on the mass of PLLA utilized to bond the PGA matrices. In addition, the bonded PGA matrices degraded much more slowly than the unbonded matrices. The PLLA bonding of PGA matrices had no effect on the ability of cells to adhere to the matrices. After 7 weeks in culture, the bonded matrices maintained 101 +/- 4% of their initial volume and an approximate original shape while the unbonded matrices contracted to 5 +/- 1% of their initial volume with an extreme change in their shape. At this time the bonded PGA matrices had a high cellularity, with smooth muscle cells (SMCs) and ECM proteins produced by these cells (e.g., elastin) filling the pores between PGA fibers. This study demonstrated that physically bonded PGA fiber-based matrices allow the maintenance of the configuration and dimensions of the original matrices and the development of a new tissue in a predefined three-dimensional structure. This approach may be useful for engineering a variety of tissues of various structures and shapes, and our study demonstrates the importance of matching both the initial mechanical properties and the degradation rate of a matrix to the specific tissue one is engineering.
聚乙醇酸(PGA)纤维的非织造网是用于组织工程的有吸引力的合成细胞外基质(ECM),已被用于构建多种类型的组织。然而,这些合成ECM缺乏结构稳定性,在组织发育过程中往往无法维持其原始结构。这使得设计具有预定义构型和尺寸的工程组织变得困难。在本研究中,我们研究了在其纤维交叉点处与第二聚合物聚-L-乳酸(PLLA)结合的基于PGA纤维的基质在体外平滑肌(SM)组织发育过程中抵抗细胞收缩力并维持其预定义结构的能力。物理结合的PGA基质的压缩模量比未结合的PGA基质增加了10至35倍,这取决于用于结合PGA基质的PLLA的质量。此外,结合的PGA基质的降解比未结合的基质慢得多。PGA基质的PLLA结合对细胞粘附于基质的能力没有影响。培养7周后,结合的基质保持其初始体积的101±4%和近似原始形状,而未结合的基质收缩至其初始体积的5±1%,形状发生极大变化。此时,结合的PGA基质具有高细胞密度,平滑肌细胞(SMC)和这些细胞产生的ECM蛋白(如弹性蛋白)填充了PGA纤维之间的孔隙。这项研究表明,物理结合的基于PGA纤维的基质能够维持原始基质的构型和尺寸,并在预定义的三维结构中发育新组织。这种方法可能对构建各种结构和形状的组织有用,我们的研究证明了使基质的初始力学性能和降解速率与所构建的特定组织相匹配的重要性。