生物
小RNA
Wnt信号通路
CTGF公司
细胞生物学
核糖核酸
祖细胞
CD90型
CD44细胞
干细胞
软骨
癌症研究
信号转导
遗传学
基因
细胞
川地34
解剖
生长因子
受体
作者
Shuai Zhang,Qier An,Peilin Hu,Xiaomin Wu,Xiaohua Pan,Wenjin Peng,Rikang Wang,Jingyi Gan,Di Chen,Zhen Li,Tianfu Wang,Guangqian Zhou
出处
期刊:Epigenomics
[Future Medicine]
日期:2019-02-18
卷期号:11 (6): 669-684
被引量:25
标识
DOI:10.2217/epi-2018-0212
摘要
Aim: To assess cartilage-derived stem/progenitor cells (CSPCs) in osteoarthritis (OA) by employing mRNA-miRNA-circRNA-lncRNA network biology approach. Methods: Differentially expressed (DE) RNAs in CSPCs from 2-/4-/8-month-old STR/Ort and CBA mice were identified to construct networks via RNA sequencing. Results: Compared with age-matched CBA mice, 4-/8-month-old STR/Ort mice had cartilage lesions and their CSPCs exhibited lower proliferative and differentiation capacity (decreased CD44 and CD90), and identified 7082 DE RNAs in STR/Ort mice were associated with strain differences or OA progression. OA-related core RNAs were identified via the networks constructed with the predominant DE RNAs, which were involved in the signaling pathways (NF-κB/MAPK/Hippo/Wnt/TGF-β/cytoskeleton organization). The core RNAs (miR-322-5p/miR-493-5p/miR-378c/CPNE1/Cdh2/PRDM16/CTGF/NCAM1) were validated in CSPCs from OA patients. Conclusion: RNA-based networks identifying core RNAs and signaling pathways contribute to CSPC-dependent OA mechanisms.
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