Altaf F M, Hering T M, Kazmi N H, Yoo J U, Johnstone B
Department of Anatomy, Case Western Reserve University, Cleveland, OH 44106, USA.
Eur Cell Mater. 2006 Nov 9;12:64-9; discussion 69-70. doi: 10.22203/ecm.v012a08.
The ATDC5 cell line exhibits the multistep chondrogenic differentiation observed during endochondral bone formation. However, it takes up to two months to complete the process of cell expansion, insulin addition to promote differentiation and further changes in culture conditions effectively to induce hypertrophy. We sought to produce consistent chondrogenesis with significant hypertrophic differentiation with simpler conditions in a more practical time period. By adding ascorbate, the prechondrogenic proliferation phase was shortened from 21 to 7 days, with production of cartilaginous nodules during the chondrogenic phase, after insulin addition, that were greater in number and larger in size. Immunohistochemistry indicated much greater matrix elaboration and the mRNA expression of sox9, aggrecan and collagen type II were all significantly increased earlier and to a much higher degree when compared with controls. Moreover, there was a robust induction of hypertrophy: Col10a1, Runx2 and Mmp13 were all induced within 7-10 days. In conclusion, addition of ascorbate to ATDC5 cultures shortened the prechondrogenic proliferation phase, produced earlier chondrogenic differentiation, heightened gene expression and robust hypertrophic differentiation, abrogating the need for extended culture times and the changes in culture conditions. This simple modification considerably enhances the practicality of this cell line for studies of chondrogenesis.
ATDC5细胞系呈现出在软骨内骨形成过程中观察到的多步骤软骨生成分化。然而,完成细胞扩增、添加胰岛素以促进分化以及有效改变培养条件以诱导肥大的过程需要长达两个月的时间。我们试图在更实际的时间段内,以更简单的条件产生一致的软骨生成并伴有显著的肥大分化。通过添加抗坏血酸盐,软骨前增殖阶段从21天缩短至7天,在添加胰岛素后的软骨生成阶段产生了数量更多、体积更大的软骨结节。免疫组织化学表明,与对照组相比,基质合成显著增加,sox9、聚集蛋白聚糖和II型胶原的mRNA表达均更早且程度更高地显著增加。此外,肥大诱导强烈:Col10a1、Runx2和Mmp13均在7 - 10天内被诱导。总之,向ATDC5培养物中添加抗坏血酸盐缩短了软骨前增殖阶段,产生了更早的软骨生成分化,提高了基因表达并增强了肥大分化,无需延长培养时间和改变培养条件。这种简单的改良大大提高了该细胞系用于软骨生成研究的实用性。