Gremlin-1 promotes IL-1β-stimulated chondrocyte inflammation and extracellular matrix degradation via activation of the MAPK signaling pathway

J Biochem Mol Toxicol. 2023 Sep;37(9):e23404. doi: 10.1002/jbt.23404. Epub 2023 Jun 23.

Abstract

The role and mechanism of Gremlin-1 in osteoarthritis (OA) were expected to be probed in this study. Firstly, an in vitro OA model was constructed by stimulating human chondrocyte cell line CHON-001 with IL-1β. Next, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) were utilized for assessing the effect of IL-1β with different concentrations (5, 10, and 20 ng/mL) on the activity and Gremlin-1 messenger RNA of CHON-001 cells, respectively. Besides, the influence of knocking down/over-expressing Gremlin-1 on the inflammatory factors (IL-6, TNF-α, IL-18 and PGE2), oxidative stress-related substances (malondialdehyde [MDA]; superoxide dismutase [SOD]; lactate dehydrogenase [LDH]), extracellular matrix (ECM) degradation-related proteins, and mitogen-activated protein kinase (MAPK) pathway proteins in IL-1β-stimulated CHON-001 cells were tested by enzyme-linked immunosorbent assay, related kits, qRT-PCR, and western blot, respectively. IL-1β inhibited CHON-001 cell proliferation and upregulated Gremlin-1 expression in a concentration-dependent manner. Overexpression of Gremlin-1 increased the IL-6, TNF-α, IL-18, PGE2, and MDA levels, enhanced the LDH activity, and decreased the SOD activity in IL-1β-induced CHON-001 cells; while the effect of Gremlin-1 knockdown on the above factors was in contrast with that of the overexpression. Furthermore, overexpression of Gremlin-1 upregulated protein expression of matrix metalloproteinase (MMP)-3, MMP-13, and ADAMTS4 while downregulated protein expression of collagen III, aggrecan, and SOX-9 in IL-1β-stimulated CHON-001 cells. Besides, overexpression of Gremlin-1 increased the p-p38/p38 value while decreased the p-JNK/JNK value in L-1β-stimulated CHON-001 cells; however, knockdown of Gremlin-1 reversed the above results. Gremlin-1 may promote IL-1β-stimulated CHON-001 cell inflammation and ECM degradation by activating the MAPK signaling pathway.

Keywords: Gremlin-1; IL-1β; extracellular matrix (ECM) degradation; mitogen-activated protein kinase (MAPK) signaling pathway; osteoarthritis (OA).

MeSH terms

  • Cells, Cultured
  • Chondrocytes / metabolism
  • Dinoprostone / metabolism
  • Extracellular Matrix / metabolism
  • Humans
  • Inflammation / chemically induced
  • Inflammation / metabolism
  • Interleukin-18 / metabolism
  • Interleukin-1beta / metabolism
  • Interleukin-1beta / pharmacology
  • Interleukin-6 / metabolism
  • MicroRNAs* / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • Osteoarthritis* / metabolism
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-18
  • Mitogen-Activated Protein Kinases
  • Tumor Necrosis Factor-alpha
  • Dinoprostone
  • Interleukin-6
  • Interleukin-1beta
  • MicroRNAs