| Literature DB >> 30464226 |
Qianyu Zhuang1, Buqing Ye2, Shangyi Hui3, Ying Du2, Robert Chunhua Zhao4, Jing Li4, Zhihong Wu1, Na Li4, Yanbin Zhang1, Hongling Li4, Shengru Wang1, Yang Yang1, Shugang Li1, Hong Zhao1, Zusen Fan5, Guixing Qiu1, Jianguo Zhang6.
Abstract
Adolescent idiopathic scoliosis (AIS) is a complex, three dimensional deformity of the spine that commonly occurs in pubescent girls. Abnormal osteogenic differentiation of mesenchymal stem cells (MSCs) is implicated in the pathogenesis of AIS. However, the biological roles of long noncoding RNAs (lncRNAs) in the regulation of osteogenic differentiation of MSCs are unknown. Through microarray analyses of bone marrow (BM) MSCs from healthy donors and AIS patients, we identified 1483 differentially expressed lncRNAs in AIS BM-MSCs. We defined a novel lncAIS (gene symbol: ENST00000453347) is dramatically downregulated in AIS BM-MSCs. In normal BM-MSCs, lncAIS interacts with NF90 to promote HOXD8 mRNA stability that enhances RUNX2 transcription in BM-MSCs, leading to osteogenic differentiation of normal BM-MSCs. By contrast, lncAIS downregualtion in AIS BM-MSCs cannot recruit NF90 and abrogates HOXD8 mRNA stability, which impedes RUNX2 transcription for osteogenic differentiation. Thereby lncAIS downregualtion in BM-MSCs suppresses osteogenic differentiation that is implicated in the pathogenesis of AIS.Entities:
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Year: 2018 PMID: 30464226 PMCID: PMC6748078 DOI: 10.1038/s41418-018-0240-2
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828