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相关概念视频

T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

13.7K
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...
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T Cell Types and Functions01:24

T Cell Types and Functions

3.2K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
3.2K
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

14.4K
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...
14.4K

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相关实验视频

Updated: May 5, 2026

Mouse Naïve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets
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Mouse Naïve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets

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CD83的表达影响了胸腺中CD4+T细胞的发育.

Yoko Fujimoto1, LiLi Tu, Ann S Miller

  • 1Department of Immunology, Duke University Medical Center, Durham, NC 27710, USA.

Cell
|April 17, 2002
PubMed
概括

CD83对于胸腺中CD4+T细胞的发育至关重要. 缺乏CD83的小鼠显示成熟的CD4+T细胞显著减少,影响免疫反应.

科学领域:

  • 免疫学 免疫学 免疫学
  • 细胞生物学 细胞生物学

背景情况:

  • 甲状腺中T淋巴细胞的发育和血统承诺取决于复杂的信号通路.
  • 甲状腺上皮细胞和树突细胞在T细胞成熟中发挥关键作用.

研究的目的:

  • 调查表面分子CD83在胸腺内CD4+T细胞发育中的作用.
  • 确定CD83缺乏对胸细胞分化和外围T细胞群的影响.

主要方法:

  • 利用CD83-缺乏的 (CD83-/-) 小鼠来研究T淋巴细胞的发育.
  • 在野生型和CD83-/-小鼠中分析了胸细胞群和外围T细胞子集.
  • 进行了细胞转移实验,使用野生类型和CD83-/- 胸细胞和骨髓干细胞.

主要成果:

  • CD83缺乏导致了CD4+单阳性胸细胞的特定发育阻断.
  • 在CD83-/-小鼠中,外围CD4+T细胞数量减少了75%-90%,主要影响了天真T细胞.
  • 胸膜细胞上的CD83表达对于成熟的CD4+T细胞的分化至关重要.

结论:

  • CD83是一个关键的调节分子 CD4+ T细胞发育在胸腺.

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Preparation of Single-Cell Suspension of Mouse Thymic Epithelial Cells and Staining of Intracellular Molecules for Flow Cytometric AnalysisMechanisms
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  • 缺少CD83导致产生功能性CD4+T细胞的严重缺陷.
  • CD83参与是适当的T淋巴细胞成熟的必要信号.