Szczerba Mateusz, Ganesh Akshaya, Gil-Marqués María Luisa, Briken Volker, Goldberg Marcia B
Center for Bacterial Pathogenesis, Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Department of Microbiology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
bioRxiv. 2025 Mar 7:2024.12.11.627830. doi: 10.1101/2024.12.11.627830.
The NLRP11 protein is only expressed in primates and participates in the activation of the canonical NLRP3 and non-canonical NLRP3 inflammasome activation after infection with gram-negative bacteria. Here, we generated a series of defined NLRP11 deletion mutants to further analyze the role of NLRP11 in NLRP3 inflammasome activation. Like the complete NLRP11 deletion mutant ( ), the NLRP11 mutant lacking the NACHT and LRR domains ( ) showed reduced activation of the canonical NLRP3 inflammasome, whereas a pyrin domain mutant ( ) had no effect on NLRP3 activation. The and mutants but not the mutant also displayed reduced activation of caspase-4 during infection with the intracytosolic, gram-negative pathogen . We found that the human adapted, acid-fast pathogen and the opportunistic pathogen both activate the non-canonical NLRP11 inflammasome in a caspase-4/5-dependent pathway. In conclusion, we show that NLRP11 functions in the non-canonical caspase-4/5 inflammasome activation pathway and the canonical NRLP3 inflammasome pathway, and that NLRP11 is required for full recognition of mycobacteria by each of these pathways. Our work extends the spectrum of bacterial pathogen recognition by the non-canonical NLRP11-caspase4/5 pathway beyond gram-negative bacteria.
NLRP11蛋白仅在灵长类动物中表达,并在革兰氏阴性菌感染后参与经典NLRP3炎性小体的激活以及非经典NLRP3炎性小体的激活。在此,我们构建了一系列明确的NLRP11缺失突变体,以进一步分析NLRP11在NLRP3炎性小体激活中的作用。与完整的NLRP11缺失突变体( )一样,缺乏NACHT和LRR结构域的NLRP11突变体( )显示经典NLRP3炎性小体的激活减少,而吡啉结构域突变体( )对NLRP3激活没有影响。 和 突变体而非 突变体在感染胞质内革兰氏阴性病原体 期间也显示半胱天冬酶-4的激活减少。我们发现,人类适应性耐酸病原体 和机会性病原体 均通过半胱天冬酶-4/5依赖性途径激活非经典NLRP11炎性小体。总之,我们表明NLRP11在非经典半胱天冬酶-4/5炎性小体激活途径和经典NRLP3炎性小体途径中发挥作用,并且NLRP11是这些途径中对分枝杆菌进行完全识别所必需的。我们的工作将非经典NLRP11-半胱天冬酶4/5途径对细菌病原体的识别范围扩展到了革兰氏阴性菌之外。