4.3 Article

AIM2 inhibits autophagy and IFN-β production during M. bovis infection

期刊

ONCOTARGET
卷 7, 期 30, 页码 46972-46987

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.10503

关键词

M. bovis; autophagy; AIM2 inflammasome; STING; Immunology and Microbiology Section; Immune response; Immunity

资金

  1. MoSTRCUK international cooperation project [2013DFG32500]
  2. National Natural Science Foundation of China [31572487]
  3. Funding of State Key Lab of Agrobiotechnology [2012SKLAB06-14]
  4. CAU Foreign Experts Major Projects [2012z018]
  5. Hign-end Foreign Experts Recruitment Program [GDW20151100036]

向作者/读者索取更多资源

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-beta 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-beta secretion.

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