An olfactory subsystem that mediates innate behaviors

调节先天行为的嗅觉子系统

• 批准号: 8757671
• 负责人: Gilad Barnea
• 金额: $ 60.17万
• 依托单位: BROWN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-06-09 至 2019-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8757671
• 关键词: Acute; Address; Afferent Neurons; Agreement; Alleles; Amines; Amygdaloid structure; Automobile Driving; Aversive Stimulus; Behavior; Behavior Control; Behavioral; Brain; Cell Separation; Chronic; Code; Collaborations; Commit; Cues; Data; Development; Dorsal; Enhancers; Ensure; Epigenetic Process; Family; Fluorescence-Activated Cell Sorting; Fluorescent Dyes; Foundations; Genes; Human; Implant; Instinct; Knock-out; Label; Laboratories; Learning; Ligands; Light; Link; Maps; Measures; Mediating; Mental disorders; Molecular; Mus; Nature; Neurons; Neurosciences; Odorant Receptors; Odors; Olfactory Epithelium; Organism; Outcome; Partner in relationship; Pattern; Pheromone; Physiological; Population; Reporter; Rodent; Running; Sensory; Smell Perception; Sorting - Cell Movement; Stereotyping; Stimulus; Structure; Study models; System; Testing; Work; base; driving behavior; insight; learned behavior; member; nervous system disorder; neuromechanism; neurophysiology; offspring; olfactory bulb; olfactory stimulus; optogenetics; preference; public health relevance; receptor; recombinase; relating to nervous system; research study; response; selective expression; stem; transcriptome sequencing; two-photon

DESCRIPTION (provided by applicant): The mammalian olfactory system responds both to neutral odors, whose significance for the organism is assigned by learning, and to odors that elicit innate behaviors. A subset of olfactory sensory neurons expresses trace amine associated receptors (TAARs) that respond to volatile amines that are mostly aversive to rodents. We recently described the projection patterns of TAAR-expressing neurons (TRNs) to the olfactory bulb and examined the molecular mechanisms that control the expression of a single TAAR per TRN. Based on these findings, our overall hypothesis is that the TRNs constitute a distinct olfactory subsystem and that they integrate into hard-wired circuits that enable them to extract specific environmental cues and drive robust innate behavioral responses. Several predictions stem from this hypothesis: 1. TRNs are molecularly distinct from ORNs and they use specific mechanisms to ensure expression of a single receptor per neuron; 2. Activation of the TRNs is sufficient to elicit innate behavioral responses and, 3. The projections from the TAAR glomeruli are stereotyped and target central neural structures appropriate to aversive behavior responses. To test these predictions, we will conduct an interdisciplinary, multi-tiered approach that spans the molecular, neuroanatomical, neurophysiological and behavioral levels. At the molecular level, we will use unbiased approaches to unequivocally determine whether TRNs express only TAARs or co-express a subset of ORs. Further, we will definitively determine whether TRNs are molecularly committed to exclusively express TAARs, or can switch to express ORs upon choosing a deleted Taar gene. We will also analyze sorted populations of TRNs to identify repressive epigenetic marks and activating enhancer sequences that control expression of a single TAAR per TRN. Together, these studies will provide the molecular evidence for defining the TRNs as a distinct olfactory subsystem. At the anatomical level, we will map the projections from the TAAR glomeruli in the bulb to higher olfactory centers in the brain. We predict that these projections will be stereotyped and these glomeruli may project predominantly to the amygdala. At the systems/behavioral level, we will determine the behavioral consequences of selective optogenetic activation of TRNs, following systematic characterization of the optimal stimuli for driving bulb responses. These experiments will test whether TAAR circuits are hard wired to induce innate behavioral responses such as sniffing, and hard wired to assign aversive valence. Our studies are the first to examine innate responses to aversive olfactory stimuli in the context of known receptors and ligands. They will shed light on the molecular and anatomical substrate of innate responses to aversive stimuli, and provide foundation for direct links between molecular and anatomical organization and behavioral outcomes. Understanding the neural mechanisms mediating the conversion of sensory information to eliciting innate behaviors may provide new insight into the underpinnings of several psychiatric conditions.

描述（由申请人提供）：哺乳动物的嗅觉系统对中性气味和引起先天行为的气味都有反应，中性气味对生物体的意义是通过学习确定的。嗅觉感觉神经元的一个子集表达痕量胺相关受体（TAAR），其对大多数啮齿动物厌恶的挥发性胺作出反应。我们最近描述了TAAR表达神经元（TRN）的投射模式，以嗅球和检查的分子机制，控制一个单一的TAAR每个TRN的表达。基于这些发现，我们的总体假设是TRN构成了一个独特的嗅觉子系统，并且它们整合到硬连线电路中，使它们能够提取特定的环境线索并驱动强大的先天行为反应。几个预测源于这个假设：1。TRN在分子上不同于ORN，它们使用特定的机制来确保每个神经元表达单个受体; 2. TRN的激活足以引起先天行为反应，3。来自TAAR肾小球的投射是定型的，并且靶向适合于厌恶行为反应的中枢神经结构。为了测试这些预测，我们将进行跨学科，多层次的方法，跨越分子，神经解剖学，神经生理学和行为水平。在分子水平上，我们将使用无偏的方法来明确确定TRN是否仅表达TAAR或共表达OR的子集。此外，我们将明确确定TRN是否在分子上专门表达TAAR，或者在选择缺失的Taar基因后可以转换为表达OR。我们还将分析TRN的分类群体，以确定抑制性表观遗传标记和激活增强子序列，控制每个TRN的单个TAAR的表达。总之，这些研究将提供分子证据定义TRNs作为一个独特的嗅觉子系统。在解剖学水平上，我们将绘制从球中的TAAR肾小球到大脑中更高级嗅觉中心的投影。我们预测这些投射将是定型的，这些肾小球可能主要投射到杏仁核。在系统/行为层面，我们将在系统表征驱动灯泡反应的最佳刺激后，确定TRN选择性光遗传学激活的行为后果。这些实验将测试TAAR回路是否是硬连线，以诱导先天的行为反应，如嗅探，和硬连线，以分配厌恶价。我们的研究是第一个检查先天反应，厌恶嗅觉刺激，在 已知受体和配体的背景。它们将揭示对厌恶刺激的先天反应的分子和解剖学基础，并为分子和解剖学组织与行为结果之间的直接联系提供基础。了解神经机制介导的感官信息的转换，引发先天行为可能会提供新的见解的基础上的几个精神疾病。