4.4 Article

Mechanical Force-Induced Specific MicroRNA Expression in Human Periodontal Ligament Stem Cells

期刊

CELLS TISSUES ORGANS
卷 199, 期 5-6, 页码 353-363

出版社

KARGER
DOI: 10.1159/000369613

关键词

Mechanical stimulation; Microarray; MicroRNAs; Network analysis; Osteogenic differentiation

资金

  1. Chinese, Shandong and Beijing Governments (National Natural Science Foundation of China) [81200758, 81470709, 81371109]
  2. Independent Innovation Foundation of Shandong University [2011GN038]
  3. Jinan Scientific Researcher Start-Up Program of University [201102066]
  4. Science and Technology Development Plan of Shandong Province [2010GSF10267]
  5. Beijing Municipality Government [PXM 2013_014226_000055, PXM2014_014226_000048, PXM2014_014226_000013, PXM2014_014226_000053, Z121100005212004, PXM 2013_014226_000021, PXM 2013_014226_07_000080, TJSHG201310025005]

向作者/读者索取更多资源

It remains unclear how the expression of microRNAs (miRNAs) in human periodontal ligament stem cells (PDLSCs) might respond to mechanical stretch. To investigate specific miRNA expression in stretched PDLSCs, we used a Flexcell (R) FX5000 (TM) tension system to achieve external mechanical stimulation. Then, a custom-designed microarray assay was performed to investigate and describe the genome-wide differential expression of miRNAs in normal and stretched PDLSCs. Finally, we implemented integrative miRNA target prediction and network analysis approaches to construct an interaction network of the key miRNAs and their putative targets. We found that stretching induced morphological changes and increased alkaline phosphatase (ALP) activity, runt-related transcription factor 2 (RUNX2), osteocalcin (OCN), and bone sialoprotein (BSP) expression in PDLSCs. The microarray data showed that 53 miRNAs were differentially expressed with stretching. With an interaction network, we examined the connections between 10 selected key miRNAs and their putative target genes, which were related to mechanical force. The results from the interaction network provided a basis for postulating the functional roles of miRNAs in PDLSCs. (C) 2015 S. Karger AG, Basel

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