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嗅觉发育与功能障碍:小胶质细胞的作用

Olfactory Development and Dysfunction: Involvement of Microglia.

作者信息

Meller Sarah J, Greer Charles A

机构信息

Departments of Neuroscience, Yale University School of Medicine, New Haven, Connecticut, United States.

Neurosurgery, Yale University School of Medicine, New Haven, Connecticut, United States.

出版信息

Physiology (Bethesda). 2025 Mar 1;40(2):0. doi: 10.1152/physiol.00037.2024. Epub 2024 Nov 5.

DOI:10.1152/physiol.00037.2024
PMID:39499248
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12183649/
Abstract

Olfactory deficits are increasingly recognized in a variety of neurological, neurodevelopmental, psychiatric, and viral diseases. While the pathology underlying olfactory loss is likely to differ across diseases, one shared feature may be an immune response mediated by microglia. Microglia orchestrate the brain's response to environmental insults and maintain neurodevelopmental homeostasis. Here, we explore the potential involvement of microglia in olfactory development and loss in disease. The effects of microglia-mediated immune response during development may be of special relevance to the olfactory system, which is unique in both its vulnerability to environmental insults as well as its extended period of neurogenesis and neuronal migration.

摘要

嗅觉缺陷在多种神经、神经发育、精神和病毒性疾病中越来越受到关注。虽然不同疾病导致嗅觉丧失的病理机制可能不同,但一个共同特征可能是由小胶质细胞介导的免疫反应。小胶质细胞协调大脑对环境损伤的反应并维持神经发育的稳态。在此,我们探讨小胶质细胞在嗅觉发育及疾病导致的嗅觉丧失中的潜在作用。小胶质细胞介导的免疫反应在发育过程中的影响可能与嗅觉系统特别相关,嗅觉系统在易受环境损伤以及神经发生和神经元迁移的延长时期方面都很独特。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/56c21150aa01/nihms-2086167-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/0f5ba909a4ce/nihms-2086167-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/b8bc21970882/nihms-2086167-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/89103c216f88/nihms-2086167-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/bdd6751aa272/nihms-2086167-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/56c21150aa01/nihms-2086167-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/0f5ba909a4ce/nihms-2086167-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/b8bc21970882/nihms-2086167-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/89103c216f88/nihms-2086167-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/bdd6751aa272/nihms-2086167-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e40/12183649/56c21150aa01/nihms-2086167-f0005.jpg

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本文引用的文献

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Distinct olfactory mucosal macrophage populations mediate neuronal maintenance and pathogen defense.不同的嗅黏膜巨噬细胞群介导神经元的维持和病原体防御。
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Inflammatory Response and Defects on Myelin Integrity in the Olfactory System of K18hACE2 Mice Infected with SARS-CoV-2.
感染 SARS-CoV-2 的 K18hACE2 小鼠嗅系统中的炎症反应和髓鞘完整性缺陷。
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Strategies to dissect microglia-synaptic interactions during aging and in Alzheimer's disease.解析衰老和阿尔茨海默病中微胶质细胞-突触相互作用的策略。
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Microglia undergo disease-associated transcriptional activation and CX3C motif chemokine receptor 1 expression regulates neurogenesis in the aged brain.小胶质细胞发生与疾病相关的转录激活,且 CX3C 基序趋化因子受体 1 的表达调节老年大脑中的神经发生。
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Activity-dependent formation of the topographic map and the critical period in the development of mammalian olfactory system.活动依赖性的拓扑图形成和哺乳类嗅觉系统发育的关键期。
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