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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...
13.7K
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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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の発現は,胸腺におけるCD4+T細胞の発達に影響する.

Yoko Fujimoto1, LiLi Tu, Ann S Miller

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

Cell
|April 17, 2002
PubMed
まとめ

CD83は,胸腺のCD4+T細胞発育に不可欠です. CD83が欠けているマウスは,成熟したCD4+T細胞の有意な減少を示し,免疫反応に影響を与えます.

科学分野:

  • 免疫学 免疫学とは
  • 細胞生物学 細胞生物学

背景:

  • 甲状腺におけるTリンパ球の発達と系統の結合は,複雑なシグナル伝達経路に依存しています.
  • 甲状腺の上皮細胞と dendritic 細胞は,T細胞の成熟に重要な役割を果たします.

研究 の 目的:

  • 甲状腺内のCD4+T細胞の発達における表面分子CD83の役割を調査する.
  • CD83欠乏がチモサイトの分化と周辺のT細胞集団に与える影響を決定する.

主な方法:

  • Tリンパ球の発達を研究するために,CD83-欠乏 (CD83-/-) のマウスを利用した.
  • ワイルド型およびCD83-/-マウスのチモサイト集団と周辺のT細胞サブセットを分析した.
  • 野生型およびCD83-/-チモサイトおよび骨髄幹細胞を用いた細胞移植実験を行った.

主要な成果:

  • CD83欠乏症は,CD4+単一陽性チモサイトにおける特定の発達ブロックを引き起こした.
  • 周辺のCD4+T細胞数は,CD83-/-マウスでは75%-90%減少し,主にネイブT細胞に影響を与えました.
  • 胸膜細胞のCD83発現は,成熟したCD4+T細胞の分化に不可欠である.

結論:

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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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Preparation of Single-Cell Suspension of Mouse Thymic Epithelial Cells and Staining of Intracellular Molecules for Flow Cytometric AnalysisMechanisms

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Last Updated: May 5, 2026

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Evaluation of T Follicular Helper Cells and Germinal Center Response During Influenza A Virus Infection in Mice
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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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Preparation of Single-Cell Suspension of Mouse Thymic Epithelial Cells and Staining of Intracellular Molecules for Flow Cytometric AnalysisMechanisms

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  • CD83は,胸腺におけるCD4+T細胞発達の重要な調節分子である.
  • CD83の欠如は,機能的なCD4+T細胞の生成に重大な欠陥をもたらします.
  • CD83のエンゲージメントは,適切なTリンパ球の成熟のために必要な信号です.