Therapeutic Effects of (5R)-5-Hydroxytriptolide on Fibroblast-Like Synoviocytes in Rheumatoid Arthritis via lncRNA WAKMAR2/miR-4478/E2F1/p53 Axis

Front Immunol. 2021 Feb 16:12:605616. doi: 10.3389/fimmu.2021.605616. eCollection 2021.

Abstract

Rheumatoid arthritis (RA) is an autoimmune disease. Fibroblast-like synoviocytes (FLS) serve a major role in synovial hyperplasia and inflammation in RA. (5R)-5-hydroxytriptolide (LLDT-8), a novel triptolide derivative, shows promising therapeutic effects for RA and is now in phase II clinical trials in China. However, the underlying mechanism of LLDT-8 is still not fully understood. Here, we found that LLDT-8 inhibited proliferation and invasion of RA FLS, as well as the production of cytokines. Microarray data demonstrated that LLDT-8 upregulated the expression of long non-coding RNA (lncRNA) WAKMAR2, which was negatively associated with proliferation and invasion of RA FLS, as well as the production of pro-inflammatory cytokines. Knockdown of WAKMAR2 abolished the inhibitory effects of LLDT-8 on RA FLS. Mechanistically, WAKMAR2 sponged miR-4478, which targeted E2F1 and downstreamed p53 signaling. Rescue experiments indicated that the inhibitory effects of LLDT-8 on RA FLS were dependent on WAKMAR2/miR-4478/E2F1/p53 axis.

Keywords: (5R)-5-hydroxytriptolide; WAKMAR2; fibroblast-like synoviocytes; inflammation; miR-4478/E2F1/p53 axis; rheumatoid arthritis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arthritis, Rheumatoid / drug therapy
  • Arthritis, Rheumatoid / etiology*
  • Arthritis, Rheumatoid / metabolism
  • Cell Proliferation / drug effects
  • Disease Susceptibility
  • Diterpenes / pharmacology*
  • Diterpenes / therapeutic use
  • E2F1 Transcription Factor / genetics*
  • E2F1 Transcription Factor / metabolism
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Gene Silencing
  • Humans
  • Macrophages / immunology
  • Macrophages / metabolism
  • MicroRNAs / genetics*
  • Models, Biological
  • RNA Interference
  • RNA, Long Noncoding / genetics*
  • Signal Transduction / drug effects
  • Synoviocytes / drug effects*
  • Synoviocytes / metabolism*
  • Synoviocytes / pathology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • Tumor Suppressor Protein p53 / genetics*
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • 5-hydroxytriptolide
  • Diterpenes
  • E2F1 Transcription Factor
  • E2F1 protein, human
  • MicroRNAs
  • RNA, Long Noncoding
  • Tumor Suppressor Protein p53