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神经元NPR-15通过秀丽隐杆线虫中的两性感觉神经元-肠道轴调节分子和行为免疫反应。

Neuronal NPR-15 modulates molecular and behavioral immune responses via the amphid sensory neuron-intestinal axis in .

作者信息

Otarigho Benson, Butts Anna Frances, Aballay Alejandro

机构信息

Department of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX.

Department of Microbiology and Molecular Genetics, McGovern Medical School at UTHealth Houston, TX.

出版信息

bioRxiv. 2024 Jan 30:2023.07.27.550570. doi: 10.1101/2023.07.27.550570.

Abstract

The survival of hosts during infections relies on their ability to mount effective molecular and behavioral immune responses. Despite extensive research on these defense strategies in various species, including the model organism , the neural mechanisms underlying their interaction remain poorly understood. Previous studies have highlighted the role of neural G protein-coupled receptors (GPCRs) in regulating both immunity and pathogen avoidance, which is particularly dependent on aerotaxis. To address this knowledge gap, we conducted a screen of mutants in neuropeptide receptor family genes. We found that loss-of-function mutations in activated immunity while suppressing pathogen avoidance behavior. Through further analysis, NPR-15 was found to regulate immunity by modulating the activity of key transcription factors, namely GATA/ELT-2 and TFEB/HLH-30. Surprisingly, the lack of pathogen avoidance of mutant animals was not influenced by oxygen levels. Moreover, our studies revealed that the amphid sensory neuron ASJ is involved in mediating the immune and behavioral responses orchestrated by NPR-15. Additionally, NPR-15 was found to regulate avoidance behavior via the TRPM gene, GON-2, which may sense the intestinal distension caused by bacterial colonization to elicit pathogen avoidance. Our study contributes to a broader understanding of host defense strategies and mechanisms underlining the interaction between molecular and behavioral immune responses.

摘要

宿主在感染期间的存活依赖于它们产生有效分子和行为免疫反应的能力。尽管对包括模式生物在内的各种物种的这些防御策略进行了广泛研究,但它们相互作用的神经机制仍知之甚少。先前的研究强调了神经G蛋白偶联受体(GPCRs)在调节免疫和病原体回避方面的作用,这尤其依赖于趋氧性。为了填补这一知识空白,我们对神经肽受体家族基因中的突变体进行了筛选。我们发现,功能丧失突变在激活免疫的同时抑制了病原体回避行为。通过进一步分析,发现NPR-15通过调节关键转录因子即GATA/ELT-2和TFEB/HLH-30的活性来调节免疫。令人惊讶的是,突变动物缺乏病原体回避不受氧气水平的影响。此外,我们的研究表明,两性感觉神经元ASJ参与介导由NPR-15协调的免疫和行为反应。此外,发现NPR-15通过TRPM基因GON-2调节回避行为,该基因可能感知由细菌定殖引起的肠道扩张以引发病原体回避。我们的研究有助于更广泛地理解宿主防御策略以及分子和行为免疫反应之间相互作用的潜在机制。

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