Styer Katie L, Singh Varsha, Macosko Evan, Steele Sarah E, Bargmann Cornelia I, Aballay Alejandro
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Science. 2008 Oct 17;322(5900):460-4. doi: 10.1126/science.1163673. Epub 2008 Sep 18.
A large body of evidence indicates that metazoan innate immunity is regulated by the nervous system, but the mechanisms involved in the process and the biological importance of such control remain unclear. We show that a neural circuit involving npr-1, which encodes a G protein-coupled receptor (GPCR) related to mammalian neuropeptide Y receptors, functions to suppress innate immune responses. The immune inhibitory function requires a guanosine 3',5'-monophosphate-gated ion channel encoded by tax-2 and tax-4 as well as the soluble guanylate cyclase GCY-35. Furthermore, we show that npr-1- and gcy-35-expressing sensory neurons actively suppress immune responses of nonneuronal tissues. A full-genome microarray analysis on animals with altered neural function due to mutation in npr-1 shows an enrichment in genes that are markers of innate immune responses, including those regulated by a conserved PMK-1/p38 mitogen-activated protein kinase signaling pathway. These results present evidence that neurons directly control innate immunity in C. elegans, suggesting that GPCRs may participate in neural circuits that receive inputs from either pathogens or infected sites and integrate them to coordinate appropriate immune responses.
大量证据表明,后生动物的先天免疫受神经系统调控,但该过程涉及的机制以及这种调控的生物学重要性仍不清楚。我们发现,一个涉及npr-1的神经回路具有抑制先天免疫反应的功能,npr-1编码一种与哺乳动物神经肽Y受体相关的G蛋白偶联受体(GPCR)。这种免疫抑制功能需要由tax-2和tax-4编码的鸟苷3',5'-单磷酸门控离子通道以及可溶性鸟苷酸环化酶GCY-35。此外,我们发现表达npr-1和gcy-35的感觉神经元能积极抑制非神经组织的免疫反应。对因npr-1突变而导致神经功能改变的动物进行的全基因组微阵列分析表明,先天免疫反应标志物相关基因出现富集,包括那些受保守的PMK-1/p38丝裂原活化蛋白激酶信号通路调控的基因。这些结果证明,线虫中的神经元可直接控制先天免疫,这表明GPCR可能参与了从病原体或感染部位接收输入信号并将其整合以协调适当免疫反应的神经回路。