...
首页> 外文期刊>Current Rheumatology Reviews >Recent Advance in Epigenetics - Application to The Regulation of Osteoclast Differentiation
【24h】

Recent Advance in Epigenetics - Application to The Regulation of Osteoclast Differentiation

机译:表观遗传学的最新进展-在破骨细胞分化调控中的应用

获取原文
获取原文并翻译 | 示例

摘要

Osteoclasts are primary cells for bone resorption, and their differentiation is tightly regulated by receptor activator of nuclear factor kappa B ligand (RANKL) and a transcription factor nuclear factor-activated T cells (NFAT) c1. Recent studies have uncovered that the epigenetic regulation such as DNA methylation, histone methylation and acetylation, and micro RNAs play a critical role in cell differentiation. In particular, the expression of key developmental genes tends to be tightly regulated by trimethylation of histone H3 lysine 4 (H3K4me3) and lysine 27 (H3K27me3). Several reports have been proposed regarding the epigenetic regulation of osteoclast differentiation including this specific histone modification change. RANKL-induced NFATc1 expression is associated with the demethylation of H3K27me3 in osteoclast precursors. Jumonji domain containing-3 (Jmjd3), a H3K27 demethylase, is induced in murine bone marrow-derived macrophages in response to RANKL stimulation, and supposedly plays a critical role in the demethylation of H3K27me3 in the Nfatc1 gene and osteoclast differentiation.
机译:破骨细胞是骨吸收的主要细胞,它们的分化受到核因子κB配体(RANKL)和转录因子核因子激活的T细胞(NFAT)c1受体激活剂的严格调控。最近的研究发现,表观遗传调控,例如DNA甲基化,组蛋白甲基化和乙酰化,以及微小RNA在细胞分化中起关键作用。特别是,关键的发育基因的表达趋于受到组蛋白H3赖氨酸4(H3K4me3)和赖氨酸27(H3K27me3)的三甲基化的严格调控。已经提出了关于破骨细胞分化的表观遗传调控的一些报道,包括这种特定的组蛋白修饰改变。 RANKL诱导的NFATc1表达与破骨细胞前体中H3K27me3的去甲基化有关。 Jumonji域包含3(Jmjd3),一种H3K27脱甲基酶,在小鼠骨髓衍生的巨噬细胞中响应RANKL刺激而被诱导,据推测在Nfatc1基因中H3K27me3的去甲基化和破骨细胞分化中起关键作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号