Swanson Michele S, Molofsky Ari B
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Autophagy. 2005 Oct-Dec;1(3):174-6. doi: 10.4161/auto.1.3.2067. Epub 2005 Oct 1.
By law in the evolutionary jungle, any host defense mechanism that efficiently kills microbes also exerts a strong selective pressure for tolerant variants to emerge. As a consequence, pathogens can be exploited as powerful tools to examine host defense mechanisms. Recent studies of the confrontation between macrophages and the opportunistic pathogen Legionella pneumophila have revealed a regulatory mechanism that may link autophagy to pyroptosis, a type of programmed cell death. Building from the extensive literature on autophagy, cell death, and innate immunity, we propose here a testable model in which the NOD-LRR protein Naip5 dictates whether murine macrophages elevate autophagy or pyroptosis as a barrier to infection.
在进化的丛林法则中,任何能有效杀灭微生物的宿主防御机制都会对耐受变体的出现施加强大的选择压力。因此,病原体可被用作研究宿主防御机制的有力工具。最近对巨噬细胞与机会性病原菌嗜肺军团菌之间对抗的研究揭示了一种可能将自噬与焦亡(一种程序性细胞死亡)联系起来的调节机制。基于关于自噬、细胞死亡和固有免疫的大量文献,我们在此提出一个可验证的模型,其中NOD-LRR蛋白Naip5决定小鼠巨噬细胞是增强自噬还是焦亡作为感染屏障。