Department of Microbiology-Immunology, University of North Carolina, Chapel Hill, NC 27599, USA.
Science. 2010 Jan 15;327(5963):286-90. doi: 10.1126/science.1184004.
NLR (nucleotide-binding domain, leucine-rich repeat-containing) proteins have rapidly emerged as central regulators of immunity and inflammation with demonstrated relevance to human diseases. Much attention has focused on the ability of several NLRs to activate the inflammasome complex and drive proteolytic processing of inflammatory cytokines; however, NLRs also regulate important inflammasome-independent functions in the immune system. We discuss several of these functions, including the regulation of canonical and noncanonical NF-kappaB activation, mitogen-activated protein kinase activation, cytokine and chemokine production, antimicrobial reactive oxygen species production, type I interferon production, and ribonuclease L activity. We also explore the mechanistic basis of these functions and describe current challenges in the field.
富含亮氨酸重复序列的核苷酸结合域(NLR)蛋白迅速成为免疫和炎症的核心调节剂,与人类疾病密切相关。人们高度关注几种 NLR 激活炎性体复合物并驱动炎性细胞因子蛋白水解加工的能力;然而,NLR 还在免疫系统中调节重要的炎性体非依赖性功能。我们讨论了其中的几个功能,包括调节经典和非经典 NF-κB 激活、丝裂原活化蛋白激酶激活、细胞因子和趋化因子产生、抗菌活性氧物质产生、Ⅰ型干扰素产生和核糖核酸酶 L 活性。我们还探讨了这些功能的机制基础,并描述了该领域当前的挑战。