Zhu Ling-Ling, Zaidi Samir, Moonga Baljit S, Troen Bruce R, Sun Li
Department of Medicine, Mount Sinai School of Medicine, New York, NY 10029, USA.
Biochem Biophys Res Commun. 2005 Jan 7;326(1):131-5. doi: 10.1016/j.bbrc.2004.10.212.
We report the program of gene expression during osteoclast formation from RAW264.7 cell precursors in response to RANK-ligand (RANK-L) using a combination of quantitative real time PCR and Affymetrix gene chip assays. We found that genes obligatory to osteoclast formation and function, namely tartrate-resistant acid phosphatase, cathepsin K, beta3 integrin, and calcitonin receptors, were up-regulated by RANK-L markedly by up to approximately 2000-fold. In contrast, we found a cluster of genes that were significantly down-regulated: these included interleukin-18, insulin-like growth factor-1, interleukin-6 receptor, and cathepsins B, C, and L. These results from real time PCR were broadly concordant with those obtained from Affymetrix. We also explored the expression of the transcription factors of the NFAT and NFkappaB family at days 3 and 5 of culture. Whereas NFATc1 expression was increased significantly at days 3 and 5 following RANK-L exposure, there were no significant increases in the expression of NFkappaB subunits, namely p65, p50, c-Rel, IkappaBalpha, and IkappaBbeta. There were also no significant differences in transcription modulator expression between days 3 and 5, except for c-Rel and NFATc4, which were both decreased significantly at day 5. The studies suggest RANK-L regulates the expression only of NFATc1, while it signals through both NFATc1 and NFkappaB.
我们运用定量实时聚合酶链反应(PCR)和Affymetrix基因芯片检测相结合的方法,报告了RAW264.7细胞前体在响应核因子κB受体活化因子配体(RANK-L)时破骨细胞形成过程中的基因表达程序。我们发现,对于破骨细胞形成和功能必不可少的基因,即抗酒石酸酸性磷酸酶、组织蛋白酶K、β3整合素和降钙素受体,被RANK-L显著上调,上调幅度高达约2000倍。相比之下,我们发现一组基因显著下调:这些基因包括白细胞介素-18、胰岛素样生长因子-1、白细胞介素-6受体以及组织蛋白酶B、C和L。实时PCR的这些结果与Affymetrix获得的结果大致一致。我们还探究了培养第3天和第5天NFAT和NFκB家族转录因子的表达情况。虽然在RANK-L暴露后的第3天和第5天NFATc1表达显著增加,但NFκB亚基,即p65、p50、c-Rel、IκBα和IκBβ的表达没有显著增加。在第3天和第5天之间,转录调节因子的表达也没有显著差异,除了c-Rel和NFATc4在第5天均显著下降。这些研究表明,RANK-L仅调节NFATc1的表达,而它通过NFATc1和NFκB两者发出信号。