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在小鼠大脑中对小胶质细胞进行可视化、示踪、消融和突变。

Visualization, Fate Mapping, Ablation, and Mutagenesis of Microglia in the Mouse Brain.

机构信息

Department of Immunology and Regenerative Biology (IRB), Weizmann Institute of Science, Rehovot, Israel.

出版信息

Adv Neurobiol. 2024;37:53-63. doi: 10.1007/978-3-031-55529-9_4.

Abstract

Since the classical studies of Pío del Río-Hortega, microglia research has come a long way. In particular, recent advances in bulk and single-cell (sc) transcriptomics have yielded many fascinating new insights into these intriguing immune cells at the interface with the central nervous system (CNS), both in small animal models and human samples. In parallel, tools developed by advanced mouse genetics have revealed the unique ontogeny of microglia and their striking dynamic interactions with other cells in the brain parenchyma. In this chapter, we will discuss various applications of the Cre/loxP-based approach that have enabled the study of microglia in their physiological context of the mouse brain. We will highlight selected key findings that have shaped our current understanding of these cells and discuss the technical intricacies of the Cre/loxP approach and some remaining challenges.

摘要

自皮奥·德尔里奥-霍尔特加(Pío del Río-Hortega)的经典研究以来,小胶质细胞研究已经取得了长足的进步。特别是,近年来批量和单细胞(sc)转录组学的进展为这些在与中枢神经系统(CNS)交界的迷人免疫细胞提供了许多新的有趣见解,无论是在小动物模型还是人类样本中。与此同时,先进的小鼠遗传学工具揭示了小胶质细胞的独特发生以及它们与脑实质中其他细胞的惊人动态相互作用。在本章中,我们将讨论 Cre/loxP 方法的各种应用,这些应用使我们能够在小鼠大脑的生理环境中研究小胶质细胞。我们将重点介绍一些关键发现,这些发现塑造了我们对这些细胞的现有理解,并讨论 Cre/loxP 方法的技术复杂性以及一些剩余的挑战。

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