The long non-coding RNA landscape of periodontal ligament stem cells subjected to compressive force

Author:

Huang Yiping1,Zhang Yingying2,Li Xiaobei1,Liu Hao1,Yang Qiaolin1,Jia Lingfei3,Zheng Yunfei1,Li Weiran14

Affiliation:

1. Department of Orthodontics, Peking University School and Hospital of Stomatology, Beijing

2. Department of Stomatology, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s Health, Beijing

3. Central Laboratory, Peking University School and Hospital of Stomatology, Beijing

4. National Clinical Research Center for Oral Diseases, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Peking University, Beijing, China

Abstract

Summary Objective The role of long non-coding ribonucleic acids (lncRNAs) during orthodontic tooth movement remains unclear. We explored the lncRNA landscape of periodontal ligament stem cells (PDLSCs) subjected to compressive force. Materials and methods PDLSCs were subjected to static compressive stress (2 g/cm2) for 12 hours. Total RNA was then extracted and sequenced to measure changes in lncRNA and messenger RNA (mRNA) expression levels. Quantitative real-time polymerase chain reaction (qRT-PCR) was used to validate the expression levels of certain lncRNAs. Differential expression analysis as well as Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were also performed. Results In total, 90 lncRNAs and 519 mRNAs were differentially expressed in PDLSCs under compressive stress. Of the lncRNAs, 72 were upregulated and 18 downregulated. The levels of eight lncRNAs of interest (FER1L4, HIF1A-AS2, MIAT, NEAT1, ADAMTS9-AS2, LUCAT1, MIR31HG, and DHFRP1) were measured via qRT-PCR, and the results were found to be consistent with those of RNA sequencing. GO and KEGG pathway analyses showed that a wide range of biological functions were expressed during compressive loading; most differentially expressed genes were involved in extracellular matrix organization, collagen fibril organization, and the cellular response to hypoxia. Conclusions The lncRNA expression profile was significantly altered in PDLSCs subjected to compressive stress. These findings expand our understanding of molecular regulation in the mechanoresponse of PDLSCs.

Funder

National Natural Science Foundation of China

Fund for Fostering Young Scholars of Peking University Health Science Center

Publisher

Oxford University Press (OUP)

Subject

Orthodontics

Reference37 articles.

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3. Investigation of multipotent postnatal stem cells from human periodontal ligament;Seo;Lancet,2004

4. Mechanical stress regulates osteogenic differentiation and RANKL/OPG ratio in periodontal ligament stem cells by the Wnt/β-catenin pathway;Zhang;Biochimica et Biophysica Acta,2016

5. Wnt5a mediated canonical Wnt signaling pathway activation in orthodontic tooth movement: possible role in the tension force-induced bone formation;Fu;Journal of Molecular Histology,2016

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