骨质疏松症
长非编码RNA
核糖核酸
小RNA
非编码RNA
去卵巢大鼠
成骨细胞
生物
计算生物学
细胞生物学
生物信息学
遗传学
基因
内分泌学
体外
雌激素
作者
Chong Yin,Ye Tian,Dijie Li,Yang Yu,Shanfeng Jiang,Yimei Hou,Meng Deng,Kaiyuan Zheng,Yan Zhang,Xiaoni Deng,Zhihao Chen,Zhiping Miao,Qiang Hao,Yu Li,Airong Qian
出处
期刊:iScience
[Cell Press]
日期:2022-02-21
卷期号:25 (3): 103949-103949
被引量:18
标识
DOI:10.1016/j.isci.2022.103949
摘要
Osteoporosis has become a high incident bone disease along with the aging of human population. Long noncoding RNAs (LncRNAs) play an important role in osteoporosis incidence. In this study, we screened out an LncRNA negatively correlated with osteoblast differentiation, which was therefore named Lnc-DIF (differentiation inhibiting factor). Functional analysis proved that Lnc-DIF inhibited bone formation. A special structure containing multiple 53 nucleotide repeats was found in the trailing end of Lnc-DIF. Our study suggested that this repeat sequence could sequester multiple miR-489-3p and inhibit bone formation through miR-489-3p/SMAD2 axis. Moreover, siRNA of Lnc-DIF would rescue bone formation in both aging and ovariectomized osteoporosis mice. This study revealed a kind of LncRNA that could function as a sponge and regulate multiple miRNAs. RNA therapy techniques that target these LncRNAs could manipulate its downstream miRNA-target pathway with significantly higher efficiency and specificity. This provided potential therapeutic insight for RNA-based therapy for osteoporosis.
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