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Changing Expression Profiles of LncRNAs, MRNAs, CircRNAs and MiRNAs During Osteoclastogenesis

Overview
Journal Sci Rep
Specialty Science
Date 2016 Feb 10
PMID 26856880
Citations 91
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Abstract

Bone is a dynamic organ continuously undergoing shaping, repairing and remodeling. The homeostasis of bone is maintained by the balance between osteoblastic bone formation and osteoclastic bone resorption. Osteoclasts (OCs) are specialized multinucleated cells derived from hematopoietic stem cells (HSCs) or monocytes/macrophage progenitor cells. There are different stages during osteoclastogenesis, and one of the most important steps to form functional osteoclasts is realized by cell-cell fusion. In our study, microarray was performed to detect the expression profiles of lncRNA, mRNA, circRNA and miRNA at different stages during osteoclastogenesis of RAW264.7 cells. Often changed RNAs were selected and clustered among the four groups with Venn analysis. The results revealed that expressions of 518 lncRNAs, 207 mRNAs, 24 circRNAs and 37 miRNAs were often altered at each stage during OC differentiation. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) biological pathway analysis were performed to predict the functions of differentially expressed lncRNAs and co-expressed potential targeting genes. Co-expression networks of lncRNA-mRNA and circRNA-miRNA were constructed based on the correlation analysis between the differentially expressed RNAs. The present study provided a systematic perspective on the potential function of non-coding RNAs (ncRNAs) during osteoclastogenesis.

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References
1.
Pierce A, Lindskog S, Hammarstrom L . Osteoclasts: structure and function. Electron Microsc Rev. 1991; 4(1):1-45. DOI: 10.1016/0892-0354(91)90015-5. View

2.
Sun Z, Cao X, Hu Z, Zhang L, Wang H, Zhou H . MiR-103 inhibits osteoblast proliferation mainly through suppressing Cav1.2 expression in simulated microgravity. Bone. 2015; 76:121-8. DOI: 10.1016/j.bone.2015.04.006. View

3.
Nigro J, Cho K, Fearon E, Kern S, Ruppert J, Oliner J . Scrambled exons. Cell. 1991; 64(3):607-13. DOI: 10.1016/0092-8674(91)90244-s. View

4.
Dou C, Zhang C, Kang F, Yang X, Jiang H, Bai Y . MiR-7b directly targets DC-STAMP causing suppression of NFATc1 and c-Fos signaling during osteoclast fusion and differentiation. Biochim Biophys Acta. 2014; 1839(11):1084-96. DOI: 10.1016/j.bbagrm.2014.08.002. View

5.
Yasui T, Hirose J, Aburatani H, Tanaka S . Epigenetic regulation of osteoclast differentiation. Ann N Y Acad Sci. 2011; 1240:7-13. DOI: 10.1111/j.1749-6632.2011.06245.x. View