Microarray analyses of lncRNAs and mRNAs expression profiling associated with diabetic peripheral neuropathy in rats

被引:22
|
作者
Guo, Guojun [1 ]
Ren, Sen [1 ]
Kang, Yu [1 ]
Liu, Yutian [1 ]
Duscher, Dominik [2 ]
Machens, Hans-Guenther [2 ]
Chen, Zhenbing [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Dept Hand Surg, Tongji Med Coll, 1277 Jiefang Ave, Wuhan 430022, Hubei, Peoples R China
[2] Tech Univ Munich, Dept Plast & Hand Surg, Munich, Germany
基金
中国国家自然科学基金;
关键词
diabetic peripheral neuropathy; dorsal root ganglia; long noncoding RNAs; microarray analysis; messenger RNAs; LONG NONCODING RNAS; P2X(3) RECEPTOR; SCIATIC-NERVE; PAIN; DYSFUNCTION; MECHANISMS; COMPONENTS; PATHWAY; MODELS;
D O I
10.1002/jcb.28802
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic peripheral neuropathy (DPN) is considered to be the most frequent neuropathic complication of diabetes, and severely affects the quality of life of patients. Long noncoding RNAs (lncRNAs) participate in various pathophysiological processes and associate with many diseases. However, the exact impact of lncRNAs on DPN remains obscure. To discover a potential connection, a microarray study was conducted to analyze the expression profiling of lncRNAs and messenger RNAs (mRNAs) in dorsal root ganglia (DRG) from streptozotocin-induced diabetic rats with DPN. As a result, 983 lncRNAs and 1357 mRNAs were aberrantly expressed compared with control samples. Using bioinformatics analyses, we identified 558 Gene Ontology terms and 94 Kyoto Encyclopedia of Genes and Genomes pathways to be significantly enriched. Additionally, the signal-net analysis indicated that integrin receptors, including Itgb3, Itgb1, Itgb8, and Itga6, might be important players in network regulation. Furthermore, the lncRNA-mRNA network analysis showed dynamic interactions between the dysregulated lncRNAs and mRNAs. This is the first study to present an overview of lncRNA and mRNA expressions in DRG tissues from DPN rats. Our results indicate that these differentially expressed lncRNAs may have crucial roles in pathological processes of DPN by regulating their coexpressed mRNAs. The data may provide novel targets for future studies, which should focus on validating their roles in the progression of DPN.
引用
收藏
页码:15347 / 15359
页数:13
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