骨不连
小RNA
微阵列
实时聚合酶链反应
微阵列分析技术
骨愈合
基因表达谱
生物
生物信息学
基因表达
细胞生物学
基因
医学
解剖
遗传学
作者
Takahiro Waki,S. Y. Lee,Takahiro Niikura,Takashi Iwakura,Yoshihiro Dogaki,Etsuko Okumachi,Ryosuke Kuroda,Masahiro Kurosaka
出处
期刊:The bone & joint journal
[British Editorial Society of Bone & Joint Surgery]
日期:2015-07-29
卷期号:97-B (8): 1144-1151
被引量:47
标识
DOI:10.1302/0301-620x.97b8.34966
摘要
MicroRNAs (miRNAs ) are small non-coding RNAs that regulate gene expression. We hypothesised that the functions of certain miRNAs and changes to their patterns of expression may be crucial in the pathogenesis of nonunion. Healing fractures and atrophic nonunions produced by periosteal cauterisation were created in the femora of 94 rats, with 1:1 group allocation. At post-fracture days three, seven, ten, 14, 21 and 28, miRNAs were extracted from the newly generated tissue at the fracture site. Microarray and real-time polymerase chain reaction (PCR) analyses of day 14 samples revealed that five miRNAs, miR-31a-3p, miR-31a-5p, miR-146a-5p, miR-146b-5p and miR-223-3p, were highly upregulated in nonunion. Real-time PCR analysis further revealed that, in nonunion, the expression levels of all five of these miRNAs peaked on day 14 and declined thereafter. Our results suggest that miR-31a-3p, miR-31a-5p, miR-146a-5p, miR-146b-5p and miR-223-3p may play an important role in the development of nonunion. These findings add to the understanding of the molecular mechanism for nonunion formation and may lead to the development of novel therapeutic strategies for its treatment. Cite this article: Bone Joint J 2015; 97-B:1144–51.
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