Yamane Shintaro, Cheng Ewana, You Zongbing, Reddi A Hari
Lawrence Ellison Center for Tissue Regeneration and Repair, Department of Orthopaedic Surgery, School of Medicine, University of California, Davis, Sacramento, California 95817, USA.
Tissue Eng. 2007 Sep;13(9):2163-73. doi: 10.1089/ten.2006.0431.
Articular cartilage is recalcitrant to repair and regeneration. Tissue engineering and regenerative medicine are potential strategies to treat the damage to articular cartilage. A thorough understanding of the gene expression profiles in articular cartilage and growth plate chondrocytes will be an important prerequisite for tissue engineering of cartilage. Regeneration is a recapitulation of embryonic development and morphogenesis. We used laser capture microdissection to capture the surface articular chondrocytes and the resting zone chondrocytes of growth plate from 14-day-old C57BL/6J mice. Total RNA was individually purified, pooled, and amplified by two rounds of in vitro transcription. Labeled cRNA probes were analyzed using the Affymetrix GeneChip Mouse Genome 430 2.0 Array. We identified 107 genes that were highly expressed by the surface articular chondrocytes and 130 genes that were highly expressed by the resting zone chondrocytes of growth plate (> or = fivefold). The expression of major matrix proteins aggrecan and collagen II were similar, while several morphogens and growth factors were differentially expressed by the surface articular chondrocytes and the resting zone chondrocytes of growth plate. The results of this investigation will be of use in the evaluation of tissue engineered cartilage.
关节软骨难以修复和再生。组织工程和再生医学是治疗关节软骨损伤的潜在策略。深入了解关节软骨和生长板软骨细胞中的基因表达谱将是软骨组织工程的重要前提。再生是胚胎发育和形态发生的重现。我们使用激光捕获显微切割技术从14日龄的C57BL/6J小鼠中捕获生长板的表面关节软骨细胞和静止区软骨细胞。分别纯化、合并总RNA,并通过两轮体外转录进行扩增。使用Affymetrix GeneChip Mouse Genome 430 2.0 Array分析标记的cRNA探针。我们鉴定出107个在表面关节软骨细胞中高表达的基因和130个在生长板静止区软骨细胞中高表达的基因(≥五倍)。主要基质蛋白聚集蛋白聚糖和胶原蛋白II的表达相似,而几种形态发生素和生长因子在表面关节软骨细胞和生长板静止区软骨细胞中差异表达。本研究结果将有助于评估组织工程软骨。