Zhang Lu, Li Qiong, Zhou Guangdong, Liu Yu, Liu Wei, Zhang Wenjie, Cao Yilin
639 Zhi Zao Ju Rd, Shanghai, China, 200011, 008613817508818;
Tissue Eng Part A. 2011 Oct 26. doi: 10.1089/ten.TEA.2011.0443.
Due to the lack of an appropriate cell source, external ear reconstruction based on tissue engineering techniques has not yet been translated to clinical applications. It has been reported that the chondrocytes from microtic cartilage can be used for cartilage regeneration. However, in our prior study, we found the passaged microtic chondrocytes became less proliferative and decreased expression of cartilage-specific markers, which would lead to the limited quantity and quality of cells from microtic cartilage to engineer an entire ear. To make full use of these cells, it is important to know whether they can provide the chondrogenic niche to promote the chondrogenesis of BMSCs. In this study, through the co-transplantation of BMSCs with microtic chondrocytes subcutaneously into nude mice, we showed that microtic chondrocytes have the potential to promote ectopic chondrogenesis of BMSCs. These results indicate that the early passage of chondrocytes from the microtic cartilage might have the same potential to promote chondrogenesis of BMSCs as normal chondrocytes. The co-culture of microtic chondrocytes with BMSCs potentially offers a practical approach to autologous ear regeneration.
由于缺乏合适的细胞来源,基于组织工程技术的外耳重建尚未转化为临床应用。据报道,小耳畸形软骨中的软骨细胞可用于软骨再生。然而,在我们之前的研究中,我们发现传代后的小耳畸形软骨细胞增殖能力下降,软骨特异性标志物的表达降低,这将导致从小耳畸形软骨中获取的细胞数量和质量有限,无法构建整个耳朵。为了充分利用这些细胞,了解它们是否能够提供软骨生成微环境以促进骨髓间充质干细胞(BMSCs)的软骨生成非常重要。在本研究中,通过将BMSCs与小耳畸形软骨细胞皮下共移植到裸鼠体内,我们发现小耳畸形软骨细胞具有促进BMSCs异位软骨生成的潜力。这些结果表明,小耳畸形软骨中早期传代的软骨细胞可能与正常软骨细胞具有相同的促进BMSCs软骨生成的潜力。小耳畸形软骨细胞与BMSCs共培养可能为自体耳再生提供一种实用的方法。