Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis Patients

Senile osteoporosis (SOP) is a worldwide age-related disease characterized by the loss of bone mass and decrease in bone strength. Bone mesenchymal stem cells (BMSCs) play an important role in the pathology of senile osteoporosis. Abnormal expression and regulation of non-coding RNA (ncRNA) are invo...

Full description

Bibliographic Details
Main Authors: Yiyun Geng, Jinfu Chen, Chongfei Chang, Yifen Zhang, Li Duan, Weimin Zhu, Lisha Mou, Jianyi Xiong, Daping Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-12-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.776984/full
_version_ 1819095758937260032
author Yiyun Geng
Yiyun Geng
Jinfu Chen
Chongfei Chang
Yifen Zhang
Li Duan
Li Duan
Weimin Zhu
Lisha Mou
Jianyi Xiong
Jianyi Xiong
Daping Wang
Daping Wang
author_facet Yiyun Geng
Yiyun Geng
Jinfu Chen
Chongfei Chang
Yifen Zhang
Li Duan
Li Duan
Weimin Zhu
Lisha Mou
Jianyi Xiong
Jianyi Xiong
Daping Wang
Daping Wang
author_sort Yiyun Geng
collection DOAJ
description Senile osteoporosis (SOP) is a worldwide age-related disease characterized by the loss of bone mass and decrease in bone strength. Bone mesenchymal stem cells (BMSCs) play an important role in the pathology of senile osteoporosis. Abnormal expression and regulation of non-coding RNA (ncRNA) are involved in a variety of human diseases. In the present study, we aimed to identify differentially expressed mRNAs and ncRNAs in senile osteoporosis patient-derived BMSCs via high-throughput transcriptome sequencing in combination with bioinformatics analysis. As a result, 415 mRNAs, 30 lncRNAs, 6 circRNAs and 27 miRNAs were found to be significantly changed in the senile osteoporosis group. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were applied to analyze the function of differentially expressed mRNAs and ncRNAs. The circRNA–miRNA–mRNA regulatory network was constructed using the cytoHubba plugin based on the Cytoscape software. Interestingly, circRNA008876-miR-150-5p-mRNA was the sole predicted circRNA-miRNA-mRNA network. The differential expression profile of this ceRNA network was further verified by qRT-PCR. The biological function of this network was validated by overexpression and knockdown experiments. In conclusion, circRNA008876-miR-150-5p-mRNA could be an important ceRNA network involved in senile osteoporosis, which provides potential biomarkers and therapeutic targets for senile osteoporosis.
first_indexed 2024-12-21T23:48:24Z
format Article
id doaj.art-f54285e9eb694f05b7046f9ad43f7316
institution Directory Open Access Journal
issn 1664-8021
language English
last_indexed 2024-12-21T23:48:24Z
publishDate 2021-12-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Genetics
spelling doaj.art-f54285e9eb694f05b7046f9ad43f73162022-12-21T18:46:00ZengFrontiers Media S.A.Frontiers in Genetics1664-80212021-12-011210.3389/fgene.2021.776984776984Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis PatientsYiyun Geng0Yiyun Geng1Jinfu Chen2Chongfei Chang3Yifen Zhang4Li Duan5Li Duan6Weimin Zhu7Lisha Mou8Jianyi Xiong9Jianyi Xiong10Daping Wang11Daping Wang12Shenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaSchool of Biotechnology and Food Engineering, Changshu Institute of Technology, Suzhou, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaGuangdong Provincial Research Center for Artificial Intelligence and Digital Orthopedic Technology, Shenzhen, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaGuangdong Provincial Research Center for Artificial Intelligence and Digital Orthopedic Technology, Shenzhen, ChinaShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People’s Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, ChinaGuangdong Provincial Research Center for Artificial Intelligence and Digital Orthopedic Technology, Shenzhen, ChinaSenile osteoporosis (SOP) is a worldwide age-related disease characterized by the loss of bone mass and decrease in bone strength. Bone mesenchymal stem cells (BMSCs) play an important role in the pathology of senile osteoporosis. Abnormal expression and regulation of non-coding RNA (ncRNA) are involved in a variety of human diseases. In the present study, we aimed to identify differentially expressed mRNAs and ncRNAs in senile osteoporosis patient-derived BMSCs via high-throughput transcriptome sequencing in combination with bioinformatics analysis. As a result, 415 mRNAs, 30 lncRNAs, 6 circRNAs and 27 miRNAs were found to be significantly changed in the senile osteoporosis group. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were applied to analyze the function of differentially expressed mRNAs and ncRNAs. The circRNA–miRNA–mRNA regulatory network was constructed using the cytoHubba plugin based on the Cytoscape software. Interestingly, circRNA008876-miR-150-5p-mRNA was the sole predicted circRNA-miRNA-mRNA network. The differential expression profile of this ceRNA network was further verified by qRT-PCR. The biological function of this network was validated by overexpression and knockdown experiments. In conclusion, circRNA008876-miR-150-5p-mRNA could be an important ceRNA network involved in senile osteoporosis, which provides potential biomarkers and therapeutic targets for senile osteoporosis.https://www.frontiersin.org/articles/10.3389/fgene.2021.776984/fullsenile osteoporosishuman bone marrow mesenchymal stem cellswhole transcriptome sequencingnon-coding RNAceRNA network
spellingShingle Yiyun Geng
Yiyun Geng
Jinfu Chen
Chongfei Chang
Yifen Zhang
Li Duan
Li Duan
Weimin Zhu
Lisha Mou
Jianyi Xiong
Jianyi Xiong
Daping Wang
Daping Wang
Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis Patients
Frontiers in Genetics
senile osteoporosis
human bone marrow mesenchymal stem cells
whole transcriptome sequencing
non-coding RNA
ceRNA network
title Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis Patients
title_full Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis Patients
title_fullStr Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis Patients
title_full_unstemmed Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis Patients
title_short Systematic Analysis of mRNAs and ncRNAs in BMSCs of Senile Osteoporosis Patients
title_sort systematic analysis of mrnas and ncrnas in bmscs of senile osteoporosis patients
topic senile osteoporosis
human bone marrow mesenchymal stem cells
whole transcriptome sequencing
non-coding RNA
ceRNA network
url https://www.frontiersin.org/articles/10.3389/fgene.2021.776984/full
work_keys_str_mv AT yiyungeng systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT yiyungeng systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT jinfuchen systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT chongfeichang systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT yifenzhang systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT liduan systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT liduan systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT weiminzhu systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT lishamou systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT jianyixiong systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT jianyixiong systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT dapingwang systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients
AT dapingwang systematicanalysisofmrnasandncrnasinbmscsofsenileosteoporosispatients