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Related Concept Videos

NF-κB-dependent Signaling Pathway02:26

NF-κB-dependent Signaling Pathway

The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The heterodimer of NF-κB...
T Cell Types and Functions01:24

T Cell Types and Functions

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...
NF-kB-dependent Signaling Pathway02:26

NF-kB-dependent Signaling Pathway

The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The heterodimer of NF-κB...
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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...
Regulation of Hematopoietic Stem Cells01:01

Regulation of Hematopoietic Stem Cells

All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
The JAK-STAT Signaling Pathway01:20

The JAK-STAT Signaling Pathway

Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...

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Related Experiment Video

Updated: May 17, 2026

NF-κB-dependent Luciferase Activation and Quantification of Gene Expression in Salmonella Infected Tissue Culture Cells
10:57

NF-κB-dependent Luciferase Activation and Quantification of Gene Expression in Salmonella Infected Tissue Culture Cells

Published on: January 12, 2020

NF-κB controls Il2 and Csf2 expression during T cell development and activation process.

Yan Li1, Stephen J Ohms, Chao Sun

  • 1College of Animal Science & Technology, Northwest A&F University, Yangling, 712100, Shaanxi, People's Republic of China.

Molecular Biology Reports
|October 20, 2012
PubMed
Summary
This summary is machine-generated.

Immune system aging involves increased inducible genes (Il2, Csf2) and memory T cells. This correlates with higher NF-κB family gene expression, suggesting a mechanism for immune dysregulation during aging.

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Area of Science:

  • Immunology
  • Cellular Aging
  • Molecular Biology

Background:

  • Immune system aging is linked to dysregulation via unclear mechanisms.
  • Factors like DNA repair efficiency, transcription factor activity (NF-κB), and cell type shifts influence aging.
  • Understanding the aging immune system is crucial.

Purpose of the Study:

  • To investigate the molecular mechanisms underlying immune system aging.
  • To examine the expression of inducible genes and cell population changes in aging T cells.

Main Methods:

  • Analysis of inducible gene expression (Il2, Csf2) during T cell activation and aging.
  • Assessment of circulating CD4(+) T cell population composition.
  • Measurement of mRNA levels for NF-κB family genes.

Main Results:

  • Inducible genes Il2 and Csf2 expression increases with T cell activation and aging.
  • A higher percentage of memory/effector T cells is observed in mature animals.
  • mRNA levels of NF-κB family genes are significantly elevated in adult mice and activated T cells.

Conclusions:

  • T cell activation and aging are associated with increased expression of inducible genes Il2 and Csf2.
  • The aging immune system exhibits a shift towards memory/effector T cells.
  • Elevated NF-κB family gene expression accompanies these changes, suggesting its role in immune aging.