Department of Prosthodontics, Peking University School and Hospital of Stomatology, Beijing, China.
Biodynamic Optical Imaging Center, College of Life Sciences, Peking University, Beijing, China.
J Bone Miner Res. 2016 Feb;31(2):391-402. doi: 10.1002/jbmr.2704. Epub 2015 Sep 30.
As the most well-studied histone acetyltransferase (HAT) in yeast and mammals, general control nonderepressible 5 (GCN5) was documented to play essential roles in various developmental processes. However, little is known about its role in osteogenic differentiation of mesenchymal stem cells (MSCs). Here, we detected the critical function of GCN5 in osteogenic commitment of MSCs. In this role, the HAT activity of GCN5 was not required. Mechanistically, GCN5 repressed nuclear factor kappa B (NF-κB)-dependent transcription and inhibited the NF-κB signaling pathway. The impaired osteogenic differentiation by GCN5 knockdown was blocked by inhibition of NF-κB. Most importantly, the expression of GCN5 was decreased significantly in the bone tissue sections of ovariectomized mice or aged mice. Collectively, these results may point to the GCN5-NF-κB pathway as a novel potential molecular target for stem cell mediated regenerative medicine and the treatment of metabolic bone diseases such as osteoporosis.
作为酵母和哺乳动物中研究最为深入的组蛋白乙酰转移酶(HAT),一般控制非阻遏 5(GCN5)被证明在各种发育过程中发挥着重要作用。然而,其在间充质干细胞(MSCs)成骨分化中的作用知之甚少。在这里,我们检测了 GCN5 在 MSCs 成骨定向中的关键作用。在这个作用中,GCN5 的 HAT 活性不是必需的。从机制上讲,GCN5 抑制核因子 kappa B(NF-κB)依赖性转录并抑制 NF-κB 信号通路。GCN5 敲低导致的成骨分化受损可被 NF-κB 抑制所阻断。最重要的是,去卵巢或衰老小鼠的骨组织切片中 GCN5 的表达明显降低。总的来说,这些结果可能表明 GCN5-NF-κB 途径是干细胞介导的再生医学和治疗骨质疏松症等代谢性骨疾病的新的潜在分子靶点。