Jove
Visualize
Contact Us

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...
Master Transcription Regulators02:23

Master Transcription Regulators

Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
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...
Forced Transdifferentiation01:28

Forced Transdifferentiation

Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial transdifferentiation occurs...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Type I interferon primes the alveolar epithelium to receive reparative signals from tissue-resident macrophages.

bioRxiv : the preprint server for biology·2026
Same author

Author Correction: Piezo1-dependent activation of stromal cells ignites muscle inflammation in exercise and injury and is associated with inflammaging.

Nature immunology·2026
Same author

Piezo1-dependent activation of stromal cells ignites muscle inflammation in exercise and injury and is associated with inflammaging.

Nature immunology·2026
Same author

Regulatory T cells safeguard liver health during metabolic-associated steatohepatitis.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Immunological knowledge.

Nature immunology·2026
Same author

The history and promise of Treg cells.

Immunity·2025
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: Jun 22, 2026

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol
08:20

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol

Published on: December 30, 2016

Foxp3+ regulatory T cells: differentiation, specification, subphenotypes.

Markus Feuerer1, Jonathan A Hill, Diane Mathis

  • 1Department of Pathology, Harvard Medical School, Boston, Massachusetts, USA.

Nature Immunology
|June 19, 2009
PubMed
Summary
This summary is machine-generated.

Regulatory T cells (Treg cells), defined by Foxp3, are complex and diverse, not just a single type. Their subphenotypes in different locations regulate immune responses, offering new insights into immune homeostasis.

Related Experiment Videos

Last Updated: Jun 22, 2026

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol
08:20

In Vitro Differentiation of Human CD4+FOXP3+ Induced Regulatory T Cells (iTregs) from Naïve CD4+ T Cells Using a TGF-β-containing Protocol

Published on: December 30, 2016

Area of Science:

  • Immunology
  • Cell Biology
  • Molecular Biology

Background:

  • Regulatory T cells (Treg cells), marked by Foxp3 expression, are crucial for maintaining immune homeostasis.
  • The traditional view of Treg cells as a uniform population solely defined by Foxp3 is evolving.
  • Emerging evidence highlights significant complexity and heterogeneity within the Treg cell compartment.

Purpose of the Study:

  • To explore the intricate diversity and subphenotypes of Treg cells.
  • To investigate the role of multiple regulatory factors beyond Foxp3 in controlling Treg cell transcriptional signatures.
  • To examine how distinct Treg cell subphenotypes contribute to immune regulation in various anatomical locations.

Main Methods:

  • Review of current literature on Treg cell biology and transcriptional regulation.
  • Analysis of studies identifying distinct Treg cell subphenotypes.
  • Examination of research on the functional specialization of Treg cell subsets.

Main Results:

  • Treg cells represent a complex population with diverse subphenotypes, not solely determined by Foxp3.
  • Multiple regulatory factors contribute to the unique transcriptional profiles of Treg cells.
  • Specific Treg cell subphenotypes are localized to different anatomical sites and regulate distinct aspects of effector T cell function.
  • Surprisingly, some Treg cell subphenotypes share transcriptional control elements with the effector cells they regulate.

Conclusions:

  • The Treg cell lineage is far more complex than previously understood, with Foxp3 being a key but not sole determinant.
  • Understanding Treg cell diversity and subphenotype-specific functions is critical for advancing immune homeostasis research.
  • The shared transcriptional elements between Treg cells and effector cells suggest intricate regulatory crosstalk.