Down-regulated in OA cartilage, SFMBT2 contributes to NF-κB-mediated ECM degradation.
Safdar HussainMengyao SunZixin MinYuanxu GuoJing XuNosheen MushtaqLisong HengHuang HuangYitong ZhaoYing YuanNazim HussainFujun ZhangYan HanPeng XuJian SunShemin LuPublished in: Journal of cellular and molecular medicine (2018)
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.
Keyphrases
- extracellular matrix
- endothelial cells
- patients undergoing
- poor prognosis
- knee osteoarthritis
- genome wide
- signaling pathway
- transcription factor
- induced pluripotent stem cells
- oxidative stress
- randomized controlled trial
- pluripotent stem cells
- stem cells
- nuclear factor
- cancer therapy
- genome wide identification
- copy number
- coronary artery disease
- gene expression
- cell proliferation
- atrial fibrillation
- toll like receptor
- resting state
- protein protein
- surgical site infection