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Mol Neurodegener. 2023 Nov 29;18(1):89. doi: 10.1186/s13024-023-00674-9.

本文引用的文献

1
Identification of a protective microglial state mediated by miR-155 and interferon-γ signaling in a mouse model of Alzheimer's disease.阿尔茨海默病小鼠模型中 miR-155 和干扰素-γ 信号介导的保护性小胶质细胞状态的鉴定。
Nat Neurosci. 2023 Jul;26(7):1196-1207. doi: 10.1038/s41593-023-01355-y. Epub 2023 Jun 8.
2
The Alzheimer's disease risk factor INPP5D restricts neuroprotective microglial responses in amyloid beta-mediated pathology.阿尔茨海默病风险因子 INPP5D 限制淀粉样β介导致病过程中的神经保护型小胶质细胞反应。
Alzheimers Dement. 2023 Nov;19(11):4908-4921. doi: 10.1002/alz.13089. Epub 2023 Apr 15.
3
INPP5D modulates TREM2 loss-of-function phenotypes in a β-amyloidosis mouse model.INPP5D在β-淀粉样变性小鼠模型中调节TREM2功能丧失表型。
iScience. 2023 Mar 13;26(4):106375. doi: 10.1016/j.isci.2023.106375. eCollection 2023 Apr 21.
4
Microglia specific deletion of miR-155 in Alzheimer's disease mouse models reduces amyloid-β pathology but causes hyperexcitability and seizures.阿尔茨海默病小鼠模型中小胶质细胞特异性 miR-155 缺失可减少淀粉样蛋白-β 病理,但导致过度兴奋和癫痫发作。
J Neuroinflammation. 2023 Mar 7;20(1):60. doi: 10.1186/s12974-023-02745-6.
5
Trem2 H157Y increases soluble TREM2 production and reduces amyloid pathology.Trem2 H157Y 增加可溶性 TREM2 的产生并减少淀粉样蛋白病理。
Mol Neurodegener. 2023 Jan 31;18(1):8. doi: 10.1186/s13024-023-00599-3.
6
INPP5D deficiency attenuates amyloid pathology in a mouse model of Alzheimer's disease.INPP5D 缺乏症可减轻阿尔茨海默病小鼠模型中的淀粉样蛋白病理。
Alzheimers Dement. 2023 Jun;19(6):2528-2537. doi: 10.1002/alz.12849. Epub 2022 Dec 16.
7
Microglial INPP5D limits plaque formation and glial reactivity in the PSAPP mouse model of Alzheimer's disease.小胶质细胞 INPP5D 限制阿尔茨海默病 PSAPP 小鼠模型中的斑块形成和神经胶质反应。
Alzheimers Dement. 2023 Jun;19(6):2239-2252. doi: 10.1002/alz.12821. Epub 2022 Nov 30.
8
Chronic TREM2 activation exacerbates Aβ-associated tau seeding and spreading.慢性 TREM2 激活加剧了 Aβ 相关 tau 种子的形成和传播。
J Exp Med. 2023 Jan 2;220(1). doi: 10.1084/jem.20220654. Epub 2022 Oct 11.
9
Elevating microglia TREM2 reduces amyloid seeding and suppresses disease-associated microglia.小胶质细胞 TREM2 的激活可减少淀粉样蛋白的形成并抑制与疾病相关的小胶质细胞。
J Exp Med. 2022 Dec 5;219(12). doi: 10.1084/jem.20212479. Epub 2022 Sep 15.
10
TREM2 modulates differential deposition of modified and non-modified Aβ species in extracellular plaques and intraneuronal deposits.TREM2 调节细胞外斑块和细胞内沉积物中修饰和未修饰 Aβ 物种的差异沉积。
Acta Neuropathol Commun. 2021 Oct 18;9(1):168. doi: 10.1186/s40478-021-01263-x.

miR155、TREM2、INPP5D:基于阿尔茨海默病淀粉样病变的小鼠模型进行临床干预时,疾病阶段和细胞类型是必须考虑的重要因素。

miR155, TREM2, INPP5D: Disease stage and cell type are essential considerations when targeting clinical interventions based on mouse models of Alzheimer's amyloidopathy.

机构信息

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.

Department of Psychiatry and Alzheimer's Disease Research Center, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.

出版信息

J Neuroinflammation. 2023 Sep 25;20(1):214. doi: 10.1186/s12974-023-02895-7.

DOI:10.1186/s12974-023-02895-7
PMID:37749581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10518910/
Abstract

Studies of microglial gene manipulation in mouse models of Alzheimer's disease (AD) amyloidopathy can cause unpredictable effects on various key endpoints, including amyloidosis, inflammation, neuritic dystrophy, neurodegeneration, and learning behavior. In this Correspondence, we discuss three examples, microRNA 155 (miR155), TREM2, and INPP5D, in which observed results have been difficult to reconcile with predicted results based on precedent, because these six key endpoints do not reliably track together. The pathogenesis of AD involves multiple cell types and complex events that may change with disease stage. We propose that cell-type targeting and timing of intervention are responsible for the sometimes impossibility of predicting whether any prospective therapeutic intervention should aim at increasing or decreasing the level or activity of a particular molecular target.

摘要

阿尔茨海默病(AD)淀粉样变的小鼠模型中对小胶质细胞基因操作的研究可能会对各种关键终点产生不可预测的影响,包括淀粉样变性、炎症、神经突营养不良、神经退行性变和学习行为。在这篇通讯中,我们讨论了三个例子,即 microRNA 155(miR155)、TREM2 和 INPP5D,观察到的结果很难与基于先例的预测结果相协调,因为这六个关键终点并不可靠地一起跟踪。AD 的发病机制涉及多种细胞类型和复杂事件,这些事件可能会随着疾病阶段的变化而变化。我们提出,细胞类型靶向和干预时机是决定某些预期治疗干预措施是否应该旨在增加或减少特定分子靶标水平或活性的有时不可能的原因。