Suppr超能文献

合成免疫突触的研究和临床应用。

Investigative and clinical applications of synthetic immune synapses.

机构信息

Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2013 Jan-Feb;5(1):75-85. doi: 10.1002/wnan.1195. Epub 2012 Aug 23.

Abstract

The immune synapse (IS) has emerged as a compelling model of cell-cell communication. This interface between a T cell and antigen-presenting cell (APC) serves as a key point in coordinating the immune response. A distinguishing feature of this interface is that juxtacrine signaling molecules form complex patterns that are defined at micrometer and submicrometer scales. Moreover, these patterns are highly dynamic. While cellular and molecular approaches have provided insight into the influence of these patterns on cell-cell signaling, replacing the APC with a synthetic, micro/nanoengineered surface promises a new level of sophistication to these studies. Micropatterning of multiple ligands onto a surface, for example, allowed the direct demonstration that T cells can sense and respond to microscale geometry of the IS. Supported lipid bilayers have captured the lateral mobility of natural ligands, allowing insight into this complex property of the cell-cell interface in model systems. Finally, engineered surfaces have allowed the study of forces and mechanosensing in T cell activation, an emerging area of immune cell research. In addition to providing new insight into biophysical principles, investigations into IS function may allow control over ex vivo T cell expansion. Bioreactors based on these concepts may find immediate application in enhancing cellular-based immunotherapy.

摘要

免疫突触 (IS) 已成为细胞间通讯的有力模型。T 细胞和抗原呈递细胞 (APC) 之间的这种界面是协调免疫反应的关键点。这个界面的一个显著特点是,旁分泌信号分子形成复杂的图案,这些图案在微米和亚微米尺度上定义。此外,这些模式具有高度动态性。虽然细胞和分子方法提供了对这些模式对细胞间信号转导影响的深入了解,但用合成的微/纳米工程表面代替 APC 有望使这些研究达到新的水平。例如,将多种配体微图案化到表面上,直接证明了 T 细胞可以感知和响应 IS 的微尺度几何形状。支持的脂质双层捕获了天然配体的横向流动性,使我们能够在模型系统中深入了解细胞间界面的这一复杂特性。最后,工程表面允许研究 T 细胞活化中的力和机械感觉,这是免疫细胞研究的一个新兴领域。除了为生物物理原理提供新的见解外,对 IS 功能的研究还可能有助于控制体外 T 细胞的扩增。基于这些概念的生物反应器可能会立即应用于增强基于细胞的免疫疗法。

相似文献

1
Investigative and clinical applications of synthetic immune synapses.合成免疫突触的研究和临床应用。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2013 Jan-Feb;5(1):75-85. doi: 10.1002/wnan.1195. Epub 2012 Aug 23.
3
Diversity in immunological synapse structure.免疫突触结构的多样性。
Immunology. 2010 Dec;131(4):466-72. doi: 10.1111/j.1365-2567.2010.03366.x. Epub 2010 Oct 29.
7
What is an immunological synapse?免疫突触是什么?
Microbes Infect. 2010 Jun;12(6):438-45. doi: 10.1016/j.micinf.2010.03.003. Epub 2010 Mar 12.
8
Microfabricated platforms to modulate and monitor T cell synapse assembly.用于调节和监测 T 细胞突触组装的微纳加工平台。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2013 Jan-Feb;5(1):67-74. doi: 10.1002/wnan.1182. Epub 2012 Aug 23.

引用本文的文献

本文引用的文献

1
Microfabricated platforms to modulate and monitor T cell synapse assembly.用于调节和监测 T 细胞突触组装的微纳加工平台。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2013 Jan-Feb;5(1):67-74. doi: 10.1002/wnan.1182. Epub 2012 Aug 23.
2
Substrate rigidity regulates human T cell activation and proliferation.基质硬度调节人 T 细胞的激活和增殖。
J Immunol. 2012 Aug 1;189(3):1330-9. doi: 10.4049/jimmunol.1102757. Epub 2012 Jun 25.
5
Mechanosensing in T lymphocyte activation.T 淋巴细胞激活中的机械感知。
Biophys J. 2012 Jan 18;102(2):L5-7. doi: 10.1016/j.bpj.2011.12.011.
9
CD4+ T-cell synapses involve multiple distinct stages.CD4+ T 细胞突触涉及多个不同的阶段。
Proc Natl Acad Sci U S A. 2011 Oct 11;108(41):17099-104. doi: 10.1073/pnas.1113703108. Epub 2011 Sep 26.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验