Department of Medical Microbiology and Immunology, School of Medicine, University of California at Davis, One Shields Avenue, Davis CA 95616, USA.
Department of Medical Microbiology and Immunology, School of Medicine, University of California at Davis, One Shields Avenue, Davis CA 95616, USA.
Trends Immunol. 2014 Mar;35(3):123-30. doi: 10.1016/j.it.2013.10.009. Epub 2013 Nov 22.
Nucleotide-binding oligomerization domain protein (NOD)1 and NOD2 participate in signaling pathways that detect pathogen-induced processes, such as the presence of peptidoglycan fragments in the host cell cytosol, as danger signals. Recent work suggests that peptidoglycan fragments activate NOD1 indirectly, through activation of the small Rho GTPase Ras-related C3 botulinum toxin substrate 1 (RAC1). Excessive activation of small Rho GTPases by virulence factors of enteric pathogens also triggers the NOD1 signaling pathway. Many enteric pathogens use virulence factors that alter the activation state of small Rho GTPases, thereby manipulating the host cell cytoskeleton of intestinal epithelial cells to promote bacterial attachment or entry. These data suggest that the NOD1 signaling pathway in intestinal epithelial cells provides an important sentinel function for detecting 'breaking and entering' by enteric pathogens.
核苷酸结合寡聚化结构域蛋白(NOD)1 和 NOD2 参与信号通路,可检测到宿主细胞胞质中病原体诱导的过程,如肽聚糖片段的存在,作为危险信号。最近的研究表明,肽聚糖片段通过激活小 Rho GTPase Ras 相关 C3 肉毒杆菌毒素底物 1(RAC1)间接激活 NOD1。肠道病原体的毒力因子过度激活小 Rho GTPases 也会触发 NOD1 信号通路。许多肠道病原体使用改变小 Rho GTPase 激活状态的毒力因子,从而操纵肠道上皮细胞的宿主细胞骨架,以促进细菌附着或进入。这些数据表明,肠道上皮细胞中的 NOD1 信号通路为检测肠道病原体的“入侵”提供了重要的哨兵功能。