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The mechanism of ascorbic acid-induced differentiation of ATDC5 chondrogenic cells.

机译:抗坏血酸诱导ATDC5软骨细胞分化的机制。

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The ATDC5 cell line exhibits a multistep process of chondrogenic differentiation analogous to that observed during endochondral bone formation. Previous investigators have induced ATDC5 cells to differentiate by exposing them to insulin at high concentrations. We have observed spontaneous differentiation of ATDC5 cells maintained in ascorbic acid-containing alpha-MEM. A comparison of the differentiation events in response to high-dose insulin vs. ascorbic acid showed similar expression patterns of key genes, including collagen II, Runx2, Sox9, Indian hedgehog, and collagen X. We took advantage of the action of ascorbic acid to examine signaling events associated with differentiation. In contrast to high-dose insulin, which downregulates both IGF-I and insulin receptors, there were only minimal changes in the abundance of these receptors during ascorbic acid-induced differentiation. Furthermore, ascorbic acid exposure was associated with ERK activation, and ERK inhibition attenuated ascorbic acid-induced differentiation. This was in contrast to the inhibitory effect of ERK activation during IGF-I-induced differentiation. Inhibition of collagen formation with a proline analog markedly attenuated the differentiating effect of ascorbic acid on ATDC5 cells. When plates were conditioned with ATDC5 cells exposed to ascorbic acid, ATDC5 cells were able to differentiate in the absence of ascorbic acid. Our results indicate that matrix formation early in the differentiation process is essential for ascorbic acid-induced ATDC5 differentiation. We conclude that ascorbic acid can promote the differentiation of ATDC5 cells by promoting the formation of collagenous matrix and that matrix formation mediates activation of the ERK signaling pathway, which promotes the differentiation program.
机译:ATDC5细胞系表现出软骨分化的多步骤过程,类似于软骨内骨形成过程中观察到的过程。先前的研究人员通过将ATDC5细胞暴露于高浓度的胰岛素中使其分化。我们已经观察到ATDC5细胞在含有抗坏血酸的alpha-MEM中自发分化。对比高剂量胰岛素与抗坏血酸的分化事件,发现关键基因的表达模式相似,包括胶原蛋白II,Runx2,Sox9,印度刺猬和胶原蛋白X。我们利用抗坏血酸的作用检查与分化相关的信号事件。与下调IGF-I和胰岛素受体的高剂量胰岛素相反,在抗坏血酸诱导的分化过程中,这些受体的丰度变化很小。此外,抗坏血酸的暴露与ERK的活化有关,而ERK的抑制作用减弱了抗坏血酸诱导的分化。这与IGF-I诱导的分化期间ERK活化的抑制作用相反。用脯氨酸类似物抑制胶原蛋白形成显着减弱了抗坏血酸对ATDC5细胞的分化作用。当板暴露于抗坏血酸的ATDC5细胞条件下,ATDC5细胞能够在不存在抗坏血酸的情况下分化。我们的结果表明,分化过程早期的基质形成对于抗坏血酸诱导的ATDC5分化至关重要。我们得出的结论是,抗坏血酸可以通过促进胶原基质的形成来促进ATDC5细胞的分化,并且基质的形成介导ERK信号通路的激活,从而促进分化程序。

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