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本文引用的文献

1
Impaired TrkB receptor signaling contributes to memory impairment in APP/PS1 mice.TrkB 受体信号转导受损导致 APP/PS1 小鼠的记忆损伤。
Neurobiol Aging. 2012 Jun;33(6):1122.e23-39. doi: 10.1016/j.neurobiolaging.2011.11.006. Epub 2011 Dec 30.
2
Postsynaptic BDNF signalling regulates long-term potentiation at thalamo-amygdala afferents.突触后 BDNF 信号调节丘脑-杏仁核传入的长时程增强。
J Physiol. 2012 Jan 1;590(1):193-208. doi: 10.1113/jphysiol.2011.220434. Epub 2011 Nov 14.
3
Blood-borne donor mast cell precursors migrate to mast cell-rich brain regions in the adult mouse.血液源性供体肥大细胞前体细胞在成年小鼠中迁移到富含肥大细胞的脑区。
J Neuroimmunol. 2011 Dec 15;240-241:142-6. doi: 10.1016/j.jneuroim.2011.09.003. Epub 2011 Oct 22.
4
Acetylcholine-synthesizing T cells relay neural signals in a vagus nerve circuit.乙酰胆碱合成 T 细胞在迷走神经回路中传递神经信号。
Science. 2011 Oct 7;334(6052):98-101. doi: 10.1126/science.1209985. Epub 2011 Sep 15.
5
Flt3L controls the development of radiosensitive dendritic cells in the meninges and choroid plexus of the steady-state mouse brain.Flt3L 控制静息状态下小鼠大脑脑膜和脉络丛中辐射敏感树突状细胞的发育。
J Exp Med. 2011 Aug 1;208(8):1695-705. doi: 10.1084/jem.20102657. Epub 2011 Jul 25.
6
Tissue-based class control: the other side of tolerance.基于组织的分类控制:耐受的另一面。
Nat Rev Immunol. 2011 Mar;11(3):221-30. doi: 10.1038/nri2940.
7
MicroRNA-124 promotes microglia quiescence and suppresses EAE by deactivating macrophages via the C/EBP-α-PU.1 pathway.miRNA-124 通过 C/EBP-α-PU.1 通路使小胶质细胞静息并抑制小胶质细胞活化从而抑制 EAE。
Nat Med. 2011 Jan;17(1):64-70. doi: 10.1038/nm.2266. Epub 2010 Dec 5.
8
Alternatively activated myeloid (M2) cells enhance cognitive function in immune compromised mice.替代性激活的髓样(M2)细胞增强免疫受损小鼠的认知功能。
Brain Behav Immun. 2011 Mar;25(3):379-85. doi: 10.1016/j.bbi.2010.11.009. Epub 2010 Nov 18.
9
Angiotensin II sustains brain inflammation in mice via TGF-beta.血管紧张素 II 通过 TGF-β 维持小鼠大脑炎症。
J Clin Invest. 2010 Aug;120(8):2782-94. doi: 10.1172/JCI41709. Epub 2010 Jul 12.
10
Regulation of learning and memory by meningeal immunity: a key role for IL-4.脑膜免疫对学习和记忆的调节:IL-4 的关键作用。
J Exp Med. 2010 May 10;207(5):1067-80. doi: 10.1084/jem.20091419. Epub 2010 May 3.

T 细胞的促认知特性。

Pro-cognitive properties of T cells.

机构信息

Center for Brain Immunology and Glia, Department of Neuroscience, School of Medicine, University of Virginia, Charlottesville, Virginia 22908, USA.

出版信息

Nat Rev Immunol. 2012 Sep;12(9):663-9. doi: 10.1038/nri3280. Epub 2012 Aug 20.

DOI:10.1038/nri3280
PMID:22903149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4032225/
Abstract

Interactions between the central nervous system and the immune system have been studied primarily in the context of pathology, popularizing the view that interplay between these two systems is inherently detrimental. However, recent experimental data have demonstrated productive neuroimmune interactions that occur under normal physiological conditions. In this Essay, we outline our current understanding of contemporary neuroimmunology, describe a working model of T cell function in support of learning and memory, and offer ideas regarding the selective advantages of immune-mediated effects on brain function.

摘要

中枢神经系统与免疫系统之间的相互作用主要是在病理学的背景下进行研究的,这使得人们普遍认为这两个系统之间的相互作用本质上是有害的。然而,最近的实验数据表明,在正常生理条件下也会发生有益的神经免疫相互作用。在这篇文章中,我们概述了我们对当代神经免疫学的理解,描述了一个支持学习和记忆的 T 细胞功能的工作模型,并提出了关于免疫介导对大脑功能的影响具有选择性优势的观点。