Key Laboratory of Targeted Intervention of Cardiovascular Disease, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine, Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China; Department of Pathology, Nantong University Affiliated Tumor Hospital, Nantong, Jiangsu, People's Republic of China.
Key Laboratory of Targeted Intervention of Cardiovascular Disease, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine, Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China.
Biochem Pharmacol. 2018 Aug;154:335-343. doi: 10.1016/j.bcp.2018.05.017. Epub 2018 May 31.
Inflammatory bowel disease is characterized by chronic intestinal inflammatory disorders associated with increased risk of developing colorectal cancer. However, the detailed mechanisms are not fully understood. The aim of this study was to determine the effect of macrophage scavenger receptor class A1 (SR-A1), a pattern recognition receptor primarily expressed in macrophages, on colitis and clarify the underlying mechanisms. We found that SR-A1 mice had an aggravating dextran sodium sulfate-induced acute and recurring colitis. This action was associated with a robust activation of both canonical and noncanonical NF-κB signaling in the colon. Suppression of the noncanonical NF-κB signaling by SR-A1 may be via its interaction with TRAF3 in macrophages. Furthermore, the anti-inflammation effect of SR-A1 could inhibit occurrence of colitis-associated cancer in mice. These results, for the first time, demonstrate that SR-A1 as a suppressor for inflammatory bowel disease.
炎症性肠病的特征是慢性肠道炎症性疾病,与结直肠癌的发病风险增加有关。然而,其详细的发病机制尚不完全清楚。本研究旨在确定巨噬细胞清道夫受体 A1(SR-A1)的作用,SR-A1 是一种主要在巨噬细胞中表达的模式识别受体,对结肠炎的影响,并阐明其潜在机制。我们发现,SR-A1 小鼠的葡聚糖硫酸钠诱导的急性和复发性结肠炎加重。这种作用与结肠中经典和非经典 NF-κB 信号的强烈激活有关。SR-A1 对非经典 NF-κB 信号的抑制作用可能是通过其在巨噬细胞中与 TRAF3 的相互作用实现的。此外,SR-A1 的抗炎作用可以抑制结肠炎相关癌症在小鼠中的发生。这些结果首次表明,SR-A1 是炎症性肠病的抑制剂。