LncRNA HOXA-AS2 positively regulates osteogenesis of mesenchymal stem cells through inactivating NF-κB signalling

被引:21
|
作者
Zhu, Xinxing [1 ,2 ]
Yu, Jinjin [3 ]
Du, Jiang [1 ,2 ]
Zhong, Genshen [4 ]
Qiao, Liang [2 ]
Lin, Juntang [1 ,2 ]
机构
[1] Xinxiang Med Univ, Coll Biomed Engn, Henan Joint Int Res Lab Stem Cell Med, Xinxiang, Peoples R China
[2] Xinxiang Med Univ, Coll Life Sci & Technol, Stem Cell & Biotherapy Engn Res Ctr Henan, Xinxiang, Peoples R China
[3] Xinxiang Med Univ, Sch Psychol, Xinxiang, Peoples R China
[4] Xinxiang Med Univ, Sch Lab Med, Henan Collaborat Innovat Ctr Mol Diag & Lab Med, Xinxiang, Peoples R China
基金
中国国家自然科学基金;
关键词
HDAC2; HOXA-AS2; lncRNA; NF-kappa B signalling; osteogenesis; INHIBITS ADIPOGENESIS; DIFFERENTIATION; PROLIFERATION; INFLAMMATION; ACTIVATION; TRANSITION; KNOCKDOWN; APOPTOSIS;
D O I
10.1111/jcmm.14034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As is previously reported, mesenchymal stem cells have potential ability to differentiate into osteocytes. However, the underlying mechanism during this biological process is poorly understood. In the present study, we identify a novel long non-coding RNA named HOXA-AS2 as a critical regulator during the formation of osteogenesis. Attenuation of HOXA-AS2 can reduce the calcium deposition and repress the alkaline phosphatase activity. Moreover, the expressions of osteogenic marker genes are markedly downregulated after HOXA-AS2 depletion. Mechanistically, we found HOXA-AS2 can regulate the transcriptional activity of NF-kappa B, a critical inhibitor of osteogenesis. More importantly, HOXA-AS2 knockdown could result in the transcriptional repression of the osteogenic master transcription factor SP7 by a NF-kappa B/HDAC2-coordinated H3K27 deacetylation mechanism. Based on these studies, we conclude that HOXA-AS2 may serve as a promising therapeutic target for bone tissue repair and regeneration in the near future.
引用
收藏
页码:1325 / 1332
页数:8
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