Ranjan Priya, Bowzard J Bradford, Schwerzmann Joy W, Jeisy-Scott Victoria, Fujita Takashi, Sambhara Suryaprakash
Influenza Division, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Trends Mol Med. 2009 Aug;15(8):359-68. doi: 10.1016/j.molmed.2009.06.003. Epub 2009 Aug 6.
The innate immune system uses pattern recognition receptors (PRRs) to sense invading microbes and initiate a rapid protective response. PRRs bind and are activated by structural motifs, such as nucleic acids or bacterial and fungal cell wall components, collectively known as pathogen-associated molecular patterns. PRRs that recognize pathogen-derived nucleic acids are present in vesicular compartments and in the cytosol of most cell types. Here, we review recent studies of these cytosolic sensors, focusing on the nature of the ligands for DNA-dependent activator of interferon (DAI)-regulatory factors, absent in melanoma 2 (AIM2), and the retinoic acid-inducible gene I-like helicase (RLH) family of receptors, the basis of ligand recognition and the signaling pathways triggered by the activation of these receptors. An increased understanding of these molecular aspects of innate immunity will guide the development of novel antiviral therapeutics.
先天性免疫系统利用模式识别受体(PRR)来感知入侵的微生物并启动快速的保护反应。PRR通过结构基序(如核酸或细菌和真菌细胞壁成分)结合并被激活,这些结构基序统称为病原体相关分子模式。识别病原体衍生核酸的PRR存在于大多数细胞类型的囊泡区室和细胞质中。在这里,我们综述了这些胞质传感器的最新研究,重点关注干扰素依赖性DNA激活剂(DAI)调节因子、黑色素瘤2缺失(AIM2)以及视黄酸诱导基因I样解旋酶(RLH)家族受体的配体性质、配体识别基础以及这些受体激活引发的信号通路。对先天性免疫这些分子方面的深入了解将指导新型抗病毒疗法的开发。