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Related Concept Videos

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...
Negative Regulator Molecules01:23

Negative Regulator Molecules

Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
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...
TGF - β Signaling Pathway01:16

TGF - β Signaling Pathway

The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors are of three kinds RI, RII, and RIII. The RI...
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form dimers that...

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Related Experiment Video

Updated: Jul 19, 2026

Isolation of Double Negative αβ T Cells from the Kidney
06:56

Isolation of Double Negative αβ T Cells from the Kidney

Published on: May 16, 2014

Double-negative regulatory T cells: non-conventional regulators.

Christopher W Thomson1, Boris P-L Lee, Li Zhang

  • 1Department of Laboratory Medicine and Pathobiology, Multi Organ Transplantation Program, Toronto General Research Institute, University Health Network, University of Toronto, Toronto, Canada.

Immunologic Research
|September 28, 2006
PubMed
Summary

Double-negative (DN) regulatory T (Treg) cells, a unique subset, inhibit immune responses by directly killing effector T cells. Understanding DN Treg cells offers insights into self-tolerance and potential therapies for various diseases.

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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
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Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells

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Related Experiment Videos

Last Updated: Jul 19, 2026

Isolation of Double Negative αβ T Cells from the Kidney
06:56

Isolation of Double Negative αβ T Cells from the Kidney

Published on: May 16, 2014

Phenotypic and Functional Analysis of Activated Regulatory T Cells Isolated from Chronic Lymphocytic Choriomeningitis Virus-infected Mice
07:17

Phenotypic and Functional Analysis of Activated Regulatory T Cells Isolated from Chronic Lymphocytic Choriomeningitis Virus-infected Mice

Published on: June 22, 2016

Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells
14:23

Generation of Induced Regulatory T Cells from Primary Human Naïve and Memory T Cells

Published on: April 16, 2012

Area of Science:

  • Immunology
  • Cell Biology

Background:

  • Regulatory T (Treg) cells are vital for maintaining self-tolerance and suppressing immune responses.
  • Distinct Treg subsets exhibit unique phenotypes and functions in various disease contexts.

Purpose of the Study:

  • To review the characteristics, development, and mechanisms of action of double-negative (DN) Treg cells.
  • To explore the role of DN Treg cells in transplant tolerance, autoimmunity, and anticancer immunity.

Main Methods:

  • Review of existing literature on DN Treg cell biology.
  • Analysis of DN Treg cell phenotypes, including expression of molecules like IFN-gamma, TNF-alpha, Ly6A, FcRgamma, and CXCR5.
  • Examination of DN Treg cell-mediated immune suppression mechanisms, including antigen-specific killing of effector T cells via MHC-peptide complexes and Fas/Fas-ligand interactions.

Main Results:

  • DN Treg cells (alphabeta-TCR+CD3+CD4-CD8-) possess potent immune-inhibitory capabilities.
  • These cells can directly kill effector T cells in an antigen-specific manner.
  • DN Treg cells express unique molecules contributing to their regulatory functions.

Conclusions:

  • Understanding DN Treg cell development and function is crucial for elucidating the loss of self-tolerance.
  • DN Treg cells represent a promising therapeutic target for immune-related diseases and transplantation.