How microglia sense and regulate neuronal activity in the adult brain

小胶质细胞如何感知和调节成人大脑中的神经元活动

• 批准号: 10671376
• 负责人: Long-Jun Wu
• 金额: $ 57.57万
• 依托单位: MAYO CLINIC ROCHESTER
• 依托单位国家: 美国
• 财政年份: 2023
• 资助国家: 美国
• 起止时间: 2023-05-15 至 2031-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10671376
• 关键词: 3-Dimensional; Acute; Adult; Anesthesia procedures; Brain; Brain Diseases; Calcium; Cells; Central Nervous System; Complex; Coupled; Electron Microscope; Epilepsy; Genetic; Hyperactivity; Immune; Knowledge; Microglia; Neurons; Norepinephrine; Outcome; Pathway interactions; Process; Purines; Research; Seizures; Severities; Signal Transduction; Sleep Disorders; Slice; Therapeutic; Virus; brain cell; conditional knockout; experience; in vivo two-photon imaging; neural circuit; neuronal circuitry; neurotransmission; receptor; reconstruction; response; tool

PROJECT SUMMARY/ABSTRACT Microglia are innate immune cells of the central nervous system, which interact with neurons in the adult brain. Microglial receptors and pathways have a demonstrated ability to alter complex network function. This process begins with microglia sensing specific neuronal signals. However, the downstream mechanisms used by microglia to enact specific responses/outcomes is not well understood. The purpose of this research is to understand how microglia sense neuronal activity during hyperactivity (e.g., seizures) and hypoactivity (e.g., anesthesia), which may then trigger unique functional responses to alter neuronal circuits in the adult brain. ATP purine signaling during hyperactivity is a well-documented signal for microglia to interact with neurons in seizure, reducing seizure severity. However, the complexity of microglial intracellular (secondary messenger such as Ca2+ signaling) responses to ATP is only partially understood. Unique intracellular signaling cascades in microglia may differentially influence their functional responses. These pathways will be interrogated using acute brain slice and in vivo two-photon imaging along with a suite of new genetic and virus-based tools to uncover how the calcium pathway of microglia in particular informs seizure responses. During hypoactivity, a loss of norepinephrine signaling allows microglia to better interact with neurons under anesthesia. The purpose of these interactions for network function is unknown, but will be dissected using in vivo two-photon imaging of microglia- neuron dynamics in the intact brain, coupled with 3D-electron microscope reconstruction of highly detailed structural interactions. Previous experience using chemogenetic and conditional knockout approaches to alter microglia function are also utilized to dissect specific pathways regulating hypoactive neural circuit responses. Ultimately, determining how microglia regulate neuronal function, including underlying mechanisms and their impact on circuitry, is essential to fully understand how microglia are integrated into the complex neuronal circuits as they become dysregulated in brain diseases, such as seizures and sleep disorders.

项目概要/摘要 小胶质细胞是中枢神经系统的先天免疫细胞，与成人大脑中的神经元相互作用。 小胶质细胞受体和通路已被证明具有改变复杂网络功能的能力。这个过程 首先是小胶质细胞感知特定的神经元信号。然而，所使用的下游机制 小胶质细胞制定特定反应/结果的机制尚不清楚。这项研究的目的是 了解小胶质细胞如何在活动过度（例如癫痫发作）和活动减退（例如癫痫发作）期间感知神经元活动 麻醉），然后可能会触发独特的功能反应，改变成人大脑中的神经元回路。 ATP 多动期间的嘌呤信号传导是小胶质细胞在癫痫发作时与神经元相互作用的一个有据可查的信号， 降低癫痫发作的严重程度。然而，小胶质细胞胞内的复杂性（第二信使，例如 Ca2+ 信号）对 ATP 的反应仅部分了解。独特的细胞内信号级联 小胶质细胞可能会不同地影响它们的功能反应。这些途径将使用急性检查 脑切片和体内双光子成像以及一套新的基于遗传和病毒的工具来揭示 小胶质细胞的钙通路如何影响癫痫反应。在活动不足期间，失去 去甲肾上腺素信号传导允许小胶质细胞在麻醉下更好地与神经元相互作用。这些的目的 网络功能的相互作用尚不清楚，但将使用小胶质细胞的体内双光子成像进行剖析 完整大脑中的神经元动力学，加上高度详细的 3D 电子显微镜重建 结构相互作用。以前使用化学遗传学和条件敲除方法改变的经验 小胶质细胞功能也被用来剖析调节低活性神经回路反应的特定途径。 最终，确定小胶质细胞如何调节神经元功能，包括潜在机制及其 对电路的影响对于充分了解小胶质细胞如何整合到复杂的神经元电路中至关重要 因为它们在癫痫和睡眠障碍等脑部疾病中变得失调。