Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

14.8K
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
14.8K
Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

1.4K
Antigen receptors are essential components of the immune system crucial in defending the body against foreign invaders. These receptors are present on the surface of B and T cells, enabling them to recognize antigens and mount an appropriate immune response.
Before encountering any antigen, lymphocytes express these receptors. On B cells, the antigen receptor is a membrane-bound antibody molecule called BCR; on T cells, it is a T cell receptor or TCR. B and T cell receptors are composed of two...
1.4K
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

16.1K
The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
16.1K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Tunable Lipid Coatings Enable Cytoplasmic siRNA Delivery by DNA Origami.

ACS applied materials & interfaces·2026
Same author

The Gibberellin 2-Oxidase Gene <i>GhGA2ox15</i> Positively Regulates Drought Resistance in Upland Cotton.

International journal of molecular sciences·2026
Same author

How to quickly determine whether patients with chronic cough need corticosteroid treatment--construction of a predictive model for corticosteroid-responsive cough in chronic cough.

NPJ primary care respiratory medicine·2026
Same author

Targeted degradation of SETDB1 by an Aptamer-CRBNL PROTAC as a novel therapeutic strategy for breast cancer.

European journal of medicinal chemistry·2026
Same author

Electrode "Cocktail Effect" Enables Charge Selective C─C Bond Cleavage of Acetonitrile for Aryl Halide Methylation.

Angewandte Chemie (International ed. in English)·2026
Same author

Metal triflimide-mediated acylation of sulfonamides and transacylation of <i>N</i>-acylsulfonamides.

Organic & biomolecular chemistry·2026

相关实验视频

Updated: Jan 18, 2026

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist
07:48

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist

Published on: April 25, 2018

6.6K

模式和精度:用于T细胞激活的空间规则的基于DNA的映射.

Shujie Li1, Kaltrina Paloja1, Maartje M C Bastings1

  • 1Programmable Biomaterials Laboratory, Institute of Materials, Interfaculty Bioengineering Institute, School of Engineering, Ecole Polytechnique Fédérale Lausanne, Lausanne, 1015, Switzerland. maartje.bastings@epfl.ch.

Nanoscale horizons
|September 11, 2025
PubMed
概括

MHC I 类 (pMHC-I) 连接体在 T 细胞上的精确排列显著增加了 T 细胞受体 (TCR) 激活. 最佳的纳米尺度间距和几何形状,就像六角形图案一样,增强了T细胞对免疫疗法设计的反应.

科学领域:

  • 免疫学 免疫学 免疫学
  • 纳米技术纳米技术
  • 生物物理学的生物物理.

背景情况:

  • T细胞受体 (TCR) 的激活对于适应性免疫非常重要.
  • -MHC I类 (pMHC-I) 连接体的纳米组织影响T细胞功能.
  • 缺乏对pMHC-I对CD8+T细胞的空间布局影响的详细理解.

研究的目的:

  • 研究pMHC-I配体的空间布局如何影响T细胞激活.
  • 为了确定连接体价值,间距,几何和灵活性在TCR信号传输中的作用.
  • 建立基于T细胞的免疫疗法的设计原则.

主要方法:

  • 利用DNA原始材料纳米材料精确控制pMHC-I空间配置.
  • 系统地改变了连接体间的间距,几何图案和分子灵活性.
  • 测量T细胞激活和信号响应.

主要成果:

  • 将连接体间距离缩小到7.5nm,T细胞活化增加了8倍.
  • 仅仅六个pMHC-I分子就足以进行强大的T细胞激活.
  • 六边形的pMHC-I装置在增强信号强度方面最有效.
  • 在pMHC-I分子之间的灵活链接器损害了TCR触发.

更多相关视频

Combined Immunofluorescence and DNA FISH on 3D-preserved Interphase Nuclei to Study Changes in 3D Nuclear Organization
13:55

Combined Immunofluorescence and DNA FISH on 3D-preserved Interphase Nuclei to Study Changes in 3D Nuclear Organization

Published on: February 3, 2013

18.9K
Real-time Live Imaging of T-cell Signaling Complex Formation
10:31

Real-time Live Imaging of T-cell Signaling Complex Formation

Published on: June 23, 2013

14.5K

相关实验视频

Last Updated: Jan 18, 2026

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist
07:48

Spatial and Temporal Control of T Cell Activation Using a Photoactivatable Agonist

Published on: April 25, 2018

6.6K
Combined Immunofluorescence and DNA FISH on 3D-preserved Interphase Nuclei to Study Changes in 3D Nuclear Organization
13:55

Combined Immunofluorescence and DNA FISH on 3D-preserved Interphase Nuclei to Study Changes in 3D Nuclear Organization

Published on: February 3, 2013

18.9K
Real-time Live Imaging of T-cell Signaling Complex Formation
10:31

Real-time Live Imaging of T-cell Signaling Complex Formation

Published on: June 23, 2013

14.5K

结论:

  • 纳米级空间参数在T细胞接口上批判性地控制pMHC-I-TCR相互作用.
  • 连接体的定义空间组织增强了T细胞激活潜力.
  • 这些发现为设计改进的T细胞免疫疗法提供了基础.