Anti-inflammatory protein TSG-6 secreted by BMSCs attenuates silica-induced acute pulmonary inflammation by inhibiting NLRP3 inflammasome signaling in macrophages

作者：Su, Wenyao; Nong, Qiying; Wu, Jie; Fan, Ruihong; Liang, Yuanting; Hu, Anyi; Gao, Zhongxiang; Liang, Weihui; Deng, Qifei; Wang, Hailan; Xia, Lihua; Huang, Yongshun; Qin, Yiru^*; Zhao, Na^*

来源：International Journal of Biological Macromolecules, 2023, 253: 126651.

DOI：10.1016/j.ijbiomac.2023.126651

• BMSCs
• TSG-6
• NLRP3 inflammasome
• Silica
• Macrophages
• Pulmonary inflammation

Silicosis is a severe occupational lung disease caused by inhalation of silica particles. Unfortunately, there are currently limited treatment options available for silicosis. Recent advances have indicated that bone marrow mesenchymal stem cells (BMSCs) have a therapeutic effect on silicosis, but their efficacy and underlying mechanisms remain largely unknown. In this study, we focused on the early phase of silica-induced lung injury to investigate the therapeutic effect of BMSCs. Our findings demonstrated that BMSCs attenuated silica-induced acute pulmonary inflammation by inhibiting NLRP3 inflammasome pathways in lung macrophages. To further understand the mechanisms involved, we utilized RNA sequencing to analyze the transcriptomes of BMSCs cocultured with silica-stimulated bone marrow-derived macrophages (BMDMs). The results clued tumor necrosis factor-stimulated gene 6 (TSG-6) might be a potentially key paracrine secretion factor released from BMSCs, which exerts a protective effect. Furthermore, the anti-inflammatory and inflammasome pathway inhibition effects of BMSCs were attenuated when TSG-6 expression was silenced, both in vivo and in vitro. Additionally, treatment with exogenous recombinant mouse TSG-6 (rmTSG-6) demonstrated similar effects to BMSCs in attenuating silica-induced inflammation. Overall, our findings suggested that BMSCs can regulate the activation of inflammasome in macrophages by secreting TSG-6, thereby protecting against silica-induced acute pulmonary inflammation both in vivo and in vitro.

• 单位
  广州医学院; 南方医科大学; 广东省人民医院; 广东医学院