<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(20)</volume><submitter>Li YX</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The precise pathogenesis of ankylosing spondylitis (AS) is still largely unknown at present. Our previous study found that toll-like receptor 4 (TLR4) downregulated and performed immunoregulatory dysfunction in mesenchymal stem cells from AS patients (AS-MSCs). The aim of this study was to explore the expression profiles of long non-coding RNAs (lncRNAs) and messenger RNAs (mRNAs) in TLR4-primed AS-MSCs, and to clarify the potential mechanisms.&lt;h4>Methods&lt;/h4>The immunoregulatory effects of MSCs were determined after TLR4 activation. Next, the differentially-expressed (DE) lncRNAs and mRNAs between AS-MSCs and TLR4-primed AS-MSCs [stimulated by lipopolysaccharide (LPS)] were identified via high-throughput sequencing followed by quantitative real-time PCR (qRT-PCR) confir</pubmed_abstract><journal>Annals of translational medicine</journal><pagination>1563</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8576702</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Integrative analysis of long non-coding RNA and messenger RNA expression in toll-like receptor 4-primed mesenchymal stem cells of ankylosing spondylitis.</pubmed_title><pmcid>PMC8576702</pmcid><pubmed_authors>Huang JJ</pubmed_authors><pubmed_authors>Lu SX</pubmed_authors><pubmed_authors>Liang YW</pubmed_authors><pubmed_authors>Liu XG</pubmed_authors><pubmed_authors>Cheng ZY</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Li YX</pubmed_authors><pubmed_authors>Huang JS</pubmed_authors><pubmed_authors>Li M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Integrative analysis of long non-coding RNA and messenger RNA expression in toll-like receptor 4-primed mesenchymal stem cells of ankylosing spondylitis.</name><description>&lt;h4>Background&lt;/h4>The precise pathogenesis of ankylosing spondylitis (AS) is still largely unknown at present. Our previous study found that toll-like receptor 4 (TLR4) downregulated and performed immunoregulatory dysfunction in mesenchymal stem cells from AS patients (AS-MSCs). The aim of this study was to explore the expression profiles of long non-coding RNAs (lncRNAs) and messenger RNAs (mRNAs) in TLR4-primed AS-MSCs, and to clarify the potential mechanisms.&lt;h4>Methods&lt;/h4>The immunoregulatory effects of MSCs were determined after TLR4 activation. Next, the differentially-expressed (DE) lncRNAs and mRNAs between AS-MSCs and TLR4-primed AS-MSCs [stimulated by lipopolysaccharide (LPS)] were identified via high-throughput sequencing followed by quantitative real-time PCR (qRT-PCR) confir</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-08T02:25:40.353Z</modification><creation>2022-02-11T13:00:37.634Z</creation></dates><accession>S-EPMC8576702</accession><cross_references><pubmed>34790769</pubmed><doi>10.21037/atm-21-5020</doi></cross_references></HashMap>