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本文引用的文献

1
Chemokines control naive CD8+ T cell selection of optimal lymph node antigen presenting cells.趋化因子控制初始 CD8+T 细胞选择最佳淋巴结抗原呈递细胞。
J Exp Med. 2011 Nov 21;208(12):2511-24. doi: 10.1084/jem.20102545. Epub 2011 Oct 31.
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In vivo two-photon microscopy to 1.6-mm depth in mouse cortex.活体小鼠皮层内 1.6 毫米深度的双光子显微镜成像。
J Biomed Opt. 2011 Oct;16(10):106014. doi: 10.1117/1.3646209.
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When multiphoton microscopy sees near infrared.当多光子显微镜看到近红外光。
Curr Opin Genet Dev. 2011 Oct;21(5):549-57. doi: 10.1016/j.gde.2011.08.004. Epub 2011 Sep 14.
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Different patterns of peripheral migration by memory CD4+ and CD8+ T cells.记忆性 CD4+ 和 CD8+ T 细胞的外周迁移的不同模式。
Nature. 2011 Aug 14;477(7363):216-9. doi: 10.1038/nature10339.
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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。
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High-resolution, noninvasive longitudinal live imaging of immune responses.高分辨率、非侵入性的免疫反应纵向活体成像。
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Intravital imaging reveals limited antigen presentation and T cell effector function in mycobacterial granulomas.活体成像揭示分枝杆菌肉芽肿中抗原呈递和 T 细胞效应功能有限。
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Two-photon absorption properties of fluorescent proteins.荧光蛋白的双光子吸收特性。
Nat Methods. 2011 May;8(5):393-9. doi: 10.1038/nmeth.1596. Epub 2011 Apr 28.
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Illuminating viral infections in the nervous system.揭示神经系统中的病毒感染。
Nat Rev Immunol. 2011 May;11(5):318-29. doi: 10.1038/nri2971.
10
Migration of cytotoxic lymphocytes in cell cycle permits local MHC I-dependent control of division at sites of viral infection.细胞毒性淋巴细胞在细胞周期中的迁移使得在病毒感染部位可以进行局部 MHC I 依赖性的分裂控制。
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活体组织中微生物免疫的双光子成像。

Two-photon imaging of microbial immunity in living tissues.

机构信息

National Institute of Neurological Disorders and Stroke, The National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Microsc Microanal. 2012 Aug;18(4):730-41. doi: 10.1017/S1431927612000281.

DOI:10.1017/S1431927612000281
PMID:22846498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3771356/
Abstract

The immune system is highly evolved and can respond to infection throughout the body. Pathogenspecific immune cells are usually generated in secondary lymphoid tissues (e.g., spleen, lymph nodes) and then migrate to sites of infection where their functionality is shaped by the local milieu. Because immune cells are so heavily influenced by the infected tissue in which they reside, it is important that their interactions and dynamics be studied in vivo. Two-photon microscopy is a powerful approach to study host-immune interactions in living tissues, and recent technical advances in the field have enabled researchers to capture movies of immune cells and infectious agents operating in real time. These studies have shed light on pathogen entry and spread through intact tissues as well as the mechanisms by which innate and adaptive immune cells participate in thwarting infections. This review focuses on how two-photon microscopy can be used to study tissue-specific immune responses in vivo, and how this approach has advanced our understanding of host-immune interactions following infection.

摘要

免疫系统高度进化,可以对全身的感染作出反应。病原体特异性免疫细胞通常在次级淋巴组织(如脾、淋巴结)中产生,然后迁移到感染部位,在那里它们的功能受到局部环境的影响。由于免疫细胞受到其所在感染组织的强烈影响,因此研究它们的相互作用和动态变化在体内进行非常重要。双光子显微镜是研究活体组织中宿主-免疫相互作用的一种强大方法,该领域最近的技术进步使研究人员能够实时拍摄免疫细胞和传染性病原体的电影。这些研究揭示了病原体通过完整组织的进入和传播,以及先天和适应性免疫细胞参与阻止感染的机制。这篇综述重点介绍了如何使用双光子显微镜在体内研究组织特异性免疫反应,以及这种方法如何提高我们对感染后宿主-免疫相互作用的理解。