Centre National de la Recherche Scientifique, Aix-Marseille Université, Institut de Biologie du Developpement de Marseille, 13009 Marseille, France.
Centre National de la Recherche Scientifique; Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement; Université Bourgogne Franche-Comté, Centre des Sciences du Goût et de l'Alimentation, L'Institut Agro Dijon, Dijon 21000, France.
J Neurosci. 2022 Oct 12;42(41):7809-7823. doi: 10.1523/JNEUROSCI.2437-21.2022. Epub 2022 Sep 8.
Probing the external world is essential for eukaryotes to distinguish beneficial from pathogenic micro-organisms. If it is clear that the main part of this task falls to the immune cells, recent work shows that neurons can also detect microbes, although the molecules and mechanisms involved are less characterized. In detection of bacteria-derived peptidoglycan by pattern recognition receptors of the peptidoglycan recognition protein (PGRP) family expressed in immune cells triggers nuclear factor-κB (-κB)/immune deficiency (IMD)-dependent signaling. We show here that one PGRP protein, called PGRP-LB, is expressed in bitter gustatory neurons of proboscises. calcium imaging in female flies reveals that the PGRP/IMD pathway is cell-autonomously required in these neurons to transduce the peptidoglycan signal. We finally show that NF-κB/IMD pathway activation in bitter-sensing gustatory neurons influences fly behavior. This demonstrates that a major immune response elicitor and signaling module are required in the peripheral nervous system to sense the presence of bacteria in the environment. In addition to the classical immune response, eukaryotes rely on neuronally controlled mechanisms to detect microbes and engage in adapted behaviors. However, the mechanisms of microbe detection by the nervous system are poorly understood. Using genetic analysis and calcium imaging, we demonstrate here that bacteria-derived peptidoglycan can activate bitter gustatory neurons. We further show that this response is mediated by the PGRP-LC membrane receptor and downstream components of a noncanonical NF-κB signaling cascade. Activation of this signaling cascade triggers behavior changes. These data demonstrate that bitter-sensing neurons and immune cells share a common detection and signaling module to either trigger the production of antibacterial effectors or to modulate the behavior of flies that are in contact with bacteria. Because peptidoglycan detection doesn't mobilize the known gustatory receptors, it also demonstrates that taste perception is much more complex than anticipated.
探测外部世界对于真核生物区分有益和致病微生物至关重要。如果说这项任务的主要部分显然落在免疫细胞上,那么最近的研究工作表明,神经元也可以检测到微生物,尽管涉及的分子和机制尚未得到充分描述。在免疫细胞中表达的肽聚糖识别蛋白(PGRP)家族的模式识别受体检测到细菌来源的肽聚糖后,会触发核因子-κB(NF-κB)/免疫缺陷(IMD)依赖性信号通路。我们在这里表明,一种名为 PGRP-LB 的 PGRP 蛋白在触角的苦味味觉神经元中表达。在雌性果蝇的钙成像中,我们发现 PGRP/IMD 通路在这些神经元中是自主需要的,以转导肽聚糖信号。我们最后表明,NF-κB/IMD 通路在苦味感觉味觉神经元中的激活会影响果蝇的行为。这表明,在周围神经系统中需要一个主要的免疫反应引发剂和信号模块来感知环境中细菌的存在。除了经典的免疫反应外,真核生物还依赖于神经元控制的机制来检测微生物并采取适应行为。然而,神经系统检测微生物的机制还知之甚少。我们使用遗传分析和钙成像,在这里证明了细菌来源的肽聚糖可以激活苦味味觉神经元。我们进一步表明,这种反应是由 PGRP-LC 膜受体和非典型 NF-κB 信号级联的下游成分介导的。该信号级联的激活触发行为变化。这些数据表明,苦味感觉神经元和免疫细胞共享一个共同的检测和信号模块,要么触发抗菌效应物的产生,要么调节与细菌接触的果蝇的行为。由于肽聚糖检测不会动员已知的味觉受体,它还表明味觉感知比预期的要复杂得多。