Down-regulated in OA cartilage, SFMBT2 contributes to NF-κB-mediated ECM degradation

J Cell Mol Med. 2018 Nov;22(11):5753-5758. doi: 10.1111/jcmm.13826. Epub 2018 Aug 22.

Abstract

The interplay between anabolic and catabolic factors regulates cartilage matrix homoeostasis. In OA, this balance is disrupted which results in cartilage degradation involving a plethora of inflammatory factors. Here, we identify a novel gene "Scm-like with four MBT domains protein 2" (SFMBT2) negatively regulated in OA cartilage. Articular cartilage from human OA patients undergoing knee arthroplasty surgery exhibited significantly decreased levels of SFMBT2 compared to the normal controls. Down-regulation of SFMBT2 by specific siRNA disturbed the metabolic homoeostasis and led to decreased expression of anabolic genes (SOX9, COL2A1) while increasing the expression of catabolic genes (MMP13 and ADAMTS4), in human chondrocytes. Finally, we revealed that SFMBT2 intervention by siRNA contributed to the catabolic phenotype of human chondrocytes mediated by NF-kB pathway.

Keywords: ECM metabolism; NF-κB; OA; SFMBT2; cartilage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Arthroplasty, Replacement, Knee*
  • Cartilage, Articular / metabolism*
  • Cartilage, Articular / pathology
  • Chondrocytes / metabolism
  • Collagen Type II / genetics
  • Female
  • Gene Expression Regulation / genetics
  • Humans
  • Male
  • Middle Aged
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Osteoarthritis / genetics*
  • Osteoarthritis / physiopathology
  • Osteoarthritis / surgery
  • RNA, Small Interfering / genetics
  • Repressor Proteins / genetics*
  • SOX9 Transcription Factor / genetics

Substances

  • COL2A1 protein, human
  • Collagen Type II
  • NF-kappa B
  • RNA, Small Interfering
  • Repressor Proteins
  • SFMBT2 protein, human
  • SOX9 Transcription Factor
  • SOX9 protein, human