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The TREM2-APOE Pathway Drives the Transcriptional Phenotype of Dysfunctional Microglia in Neurodegenerative Diseases.TREM2-载脂蛋白E通路驱动神经退行性疾病中功能失调的小胶质细胞的转录表型。
Immunity. 2017 Sep 19;47(3):566-581.e9. doi: 10.1016/j.immuni.2017.08.008.
2
LRRK2 levels in immune cells are increased in Parkinson's disease.帕金森病患者免疫细胞中的LRRK2水平升高。
NPJ Parkinsons Dis. 2017 Mar 28;3:11. doi: 10.1038/s41531-017-0010-8. eCollection 2017.
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A Unique Microglia Type Associated with Restricting Development of Alzheimer's Disease.一种与限制阿尔茨海默病发展相关的独特小胶质细胞类型。
Cell. 2017 Jun 15;169(7):1276-1290.e17. doi: 10.1016/j.cell.2017.05.018. Epub 2017 Jun 8.
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Complement C3 deficiency protects against neurodegeneration in aged plaque-rich APP/PS1 mice.补体C3缺乏可预防老年富含斑块的APP/PS1小鼠的神经退行性变。
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An environment-dependent transcriptional network specifies human microglia identity.一个依赖环境的转录网络决定了人类小胶质细胞的特性。
Science. 2017 Jun 23;356(6344). doi: 10.1126/science.aal3222. Epub 2017 May 25.
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Analysis of monocyte infiltration in MPTP mice reveals that microglial CX3CR1 protects against neurotoxic over-induction of monocyte-attracting CCL2 by astrocytes.对MPTP小鼠单核细胞浸润的分析表明,小胶质细胞CX3CR1可防止星形胶质细胞过度诱导产生吸引单核细胞的CCL2所导致的神经毒性。
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Disease Progression-Dependent Effects of TREM2 Deficiency in a Mouse Model of Alzheimer's Disease.阿尔茨海默病小鼠模型中TREM2缺乏对疾病进展的依赖性影响
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Early changes in CSF sTREM2 in dominantly inherited Alzheimer's disease occur after amyloid deposition and neuronal injury.在显性遗传性阿尔茨海默病中,CSF sTREM2 的早期变化发生在淀粉样蛋白沉积和神经元损伤之后。
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小胶质细胞和单核细胞在神经退行性疾病中的差异贡献。

Differential contribution of microglia and monocytes in neurodegenerative diseases.

机构信息

Ann Romney Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Evergrande Center for Immunologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

J Neural Transm (Vienna). 2018 May;125(5):809-826. doi: 10.1007/s00702-017-1795-7. Epub 2017 Oct 23.

DOI:10.1007/s00702-017-1795-7
PMID:29063348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7255107/
Abstract

Neuroinflammation is a hallmark of neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS). Microglia, the innate immune cells of the CNS, are the first to react to pathological insults. However, multiple studies have also demonstrated an involvement of peripheral monocytes in several neurodegenerative diseases. Due to the different origins of these two cell types, it is important to distinguish their role and function in the development and progression of these diseases. In this review, we will summarize and discuss the current knowledge of the differential contributions of microglia and monocytes in the common neurodegenerative diseases AD, PD, and ALS, as well as multiple sclerosis, which is now regarded as a combination of inflammatory processes and neurodegeneration. Until recently, it has been challenging to differentiate microglia from monocytes, as there were no specific markers. Therefore, the recent identification of specific molecular signatures of both cell types will help to advance our understanding of their differential contribution in neurodegenerative diseases.

摘要

神经炎症是包括阿尔茨海默病(AD)、帕金森病(PD)和肌萎缩侧索硬化症(ALS)在内的神经退行性疾病的一个标志。小胶质细胞是中枢神经系统的固有免疫细胞,是对病理损伤的第一反应者。然而,多项研究也表明,外周单核细胞参与了几种神经退行性疾病。由于这两种细胞类型的起源不同,区分它们在这些疾病的发展和进展中的作用和功能非常重要。在这篇综述中,我们将总结和讨论小胶质细胞和单核细胞在常见神经退行性疾病 AD、PD 和 ALS 以及多发性硬化症(MS)中的不同作用,MS 现在被认为是炎症过程和神经退行性变的结合。直到最近,由于没有特定的标志物,区分小胶质细胞和单核细胞仍然具有挑战性。因此,最近确定了这两种细胞类型的特定分子特征,这将有助于我们深入了解它们在神经退行性疾病中的差异贡献。