Key Laboratory of Diagnostic Medicine Designated by the Chinese Ministry of Education, Chongqing Medical University, Chongqing, PR China.
BMB Rep. 2013 Aug;46(8):422-7. doi: 10.5483/bmbrep.2013.46.8.266.
Although BMP9 is highly capable of promoting osteogenic differentiation of mesenchymal stem cell (MSCs), the molecular mechanism involved remains to be fully elucidated. Here, we explore the possible involvement and detail role of JNKs (c-Jun N-terminal kinases) in BMP9-induced osteogenic differentiation of MSCs. It was found that BMP9 stimulated the activation of JNKs in MSCs. BMP9-induced osteogenic differentiation of MSCs was dramatically inhibited by JNKs inhibitor SP600125. Moreover, BMP9-activated Smads signaling was decreased by SP600125 treatment in MSCs. The effects of inhibitor are reproduced with adenoviruses expressing siRNA targeted JNKs. Taken together, our results revealed that JNKs was activated in BMP9-induced osteogenic differentiation of MSCs. What is most noteworthy, however, is that inhibition of JNKs activity resulted in reduction of BMP9-induced osteogenic differentiation of MSCs, implying that activation of JNKs is essential for BMP9 osteoinductive activity.
虽然 BMP9 非常能够促进间充质干细胞(MSCs)的成骨分化,但涉及的分子机制仍有待充分阐明。在这里,我们探讨了 JNKs(c-Jun N-末端激酶)在 BMP9 诱导的 MSCs 成骨分化中的可能作用和详细作用。结果发现,BMP9 刺激了 JNKs 在 MSCs 中的激活。JNKs 抑制剂 SP600125 显著抑制了 BMP9 诱导的 MSCs 成骨分化。此外,SP600125 处理还降低了 BMP9 激活的 Smads 信号在 MSCs 中的表达。用表达靶向 JNKs 的 siRNA 的腺病毒进行的抑制剂实验重现了这些结果。总之,我们的研究结果揭示了 JNKs 在 BMP9 诱导的 MSCs 成骨分化中被激活。然而,最值得注意的是,抑制 JNKs 的活性导致 BMP9 诱导的 MSCs 成骨分化减少,这意味着 JNKs 的激活对于 BMP9 的成骨活性是必不可少的。