Zhai Qiaoli, Zhao Yi, Wang Linping, Dai Yan, Zhao Peiqing, Xiang Xinxin, Liu Kui, Du Wenyan, Tian Wenxiu, Yang Baoye, Li Tao, Wang Lianqing
Center of Translational Medicine, Zibo Central Hospital, Shandong University, Zibo, China.
School of Stomatology, Shandong University, Jinan, China.
Front Cell Dev Biol. 2020 Dec 11;8:602731. doi: 10.3389/fcell.2020.602731. eCollection 2020.
Circular RNAs (circRNAs) are regarded as pivotal regulators in bone metabolism. However, the role of circRNAs in osteoblast mineralization remains largely unknown. Herein, we explored the expression profiles of circRNAs in 4 groups of osteoblasts with varying mineralization processes. Hsa_circ_0008500 (circ8500), which is upregulated in the RNA-seq data, is sifted through 194 candidate circRNAs in osteoblasts during mineralization. We characterize the features of novel circRNAs and find that the elevated expression of circ8500 promotes osteoblast mineralization. Mechanistically, circ8500 contains a critical binding site for miR-1301-3p. We further show that circ8500 competitively binds miR-1301-3p to abolish its suppressive effect on peptidyl arginine deiminase 4 (PADI4). PADI4 works as a binding partner of RUNX2 and stabilizes its protein expression levels by inhibiting the ubiquitin-proteasome pathway. This work provides new insights on the circRNA patterns in osteoblasts and the role of PADI4 in matrix mineralization.
环状RNA(circRNAs)被认为是骨代谢中的关键调节因子。然而,circRNAs在成骨细胞矿化中的作用仍 largely未知。在此,我们探索了4组成骨细胞在不同矿化过程中circRNAs的表达谱。在RNA测序数据中上调的hsa_circ_0008500(circ8500),是从矿化过程中成骨细胞的194个候选circRNAs中筛选出来的。我们表征了新circRNAs的特征,并发现circ8500的表达升高促进成骨细胞矿化。机制上,circ8500包含一个与miR-1301-3p的关键结合位点。我们进一步表明,circ8500竞争性结合miR-1301-3p,以消除其对肽基精氨酸脱亚氨酶4(PADI4)的抑制作用。PADI4作为RUNX2的结合伙伴,通过抑制泛素-蛋白酶体途径稳定其蛋白表达水平。这项工作为成骨细胞中的circRNA模式以及PADI4在基质矿化中的作用提供了新的见解。