Liu Chunfa, Yue Ruichao, Yang Yang, Cui Yongyong, Yang Lifeng, Zhao Deming, Zhou Xiangmei
State Key Laboratories for Agrobiotechnology, Key Laboratory of Animal Epidemiology and Zoonosis, Ministry of Agriculture, National Animal Transmissible Spongiform Encephalopathy Laboratory, College of Veterinary Medicine, China Agricultural University, Beijing, China.
College of Animal Sciences and Technology, Zhejiang A&F University, Lin'an, China.
Oncotarget. 2016 Jul 26;7(30):46972-46987. doi: 10.18632/oncotarget.10503.
Mycobacteria can trigger the AIM2 inflammasome, autophagy activation and type-I interferon release, which are both activated by cytosolic DNA. We have recently demonstrated that activation of the AIM2 inflammasome during M. bovis infection is the result of mycobacterial translocation into the cytosol. To elucidate the effects of inflammasome activation on autophagy, we investigated the role of the AIM2 inflammasome from macrophages infected with a virulent strain of M. bovis. The results showed that the M. bovis-induced AIM2 inflammasome activation decreases autophagy in immortalized and primary murine macrophages. This relied on the inflammasome sensor AIM2 which conjugates with cytosolic DNA to inhibit the STING-dependent pathway involved in selective autophagy and interferon-β release in Mycobacterium-infected macrophages. These results suggest that the AIM2 cytosolic DNA sensor may conjugate competitively with cytosolic M. bovis DNA to restrict M. bovis induced STING-TBK1-dependent autophagy activation and IFN-β secretion.
分枝杆菌可触发AIM2炎性小体、自噬激活和I型干扰素释放,这些均由胞质DNA激活。我们最近证明,牛分枝杆菌感染期间AIM2炎性小体的激活是分枝杆菌转运至胞质溶胶的结果。为阐明炎性小体激活对自噬的影响,我们研究了AIM2炎性小体在感染强毒株牛分枝杆菌的巨噬细胞中的作用。结果表明,牛分枝杆菌诱导的AIM2炎性小体激活可降低永生化和原代小鼠巨噬细胞中的自噬。这依赖于炎性小体传感器AIM2,它与胞质DNA结合,以抑制分枝杆菌感染的巨噬细胞中参与选择性自噬和干扰素-β释放的STING依赖性途径。这些结果表明,AIM2胞质DNA传感器可能与胞质牛分枝杆菌DNA竞争性结合,以限制牛分枝杆菌诱导的STING-TBK1依赖性自噬激活和IFN-β分泌。