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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...
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a rapamycin-insensitive companion...
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...
Interactions Between Signaling Pathways01:19

Interactions Between Signaling Pathways

Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
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 19, 2026

Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation
15:33

Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation

Published on: August 13, 2013

Does the PI3K pathway promote or antagonize regulatory T cell development and function?

Dalya R Soond1, Elizabeth C M Slack, Oliver A Garden

  • 1Laboratory of Lymphocyte Signalling and Development, Babraham Institute Cambridge, UK.

Frontiers in Immunology
|August 23, 2012
PubMed
Summary

Regulatory T cells (Tregs) play a crucial role in preventing autoimmunity. This study reconciles conflicting research on phosphoinositide 3-kinase (PI3K) signaling

Keywords:
AktFoxoPI3KT cellTregautoimmunityinflammationmTOR

More Related Videos

Retroviral Transduction of Helper T Cells as a Genetic Approach to Study Mechanisms Controlling their Differentiation and Function
11:50

Retroviral Transduction of Helper T Cells as a Genetic Approach to Study Mechanisms Controlling their Differentiation and Function

Published on: November 4, 2016

Related Experiment Videos

Last Updated: May 19, 2026

Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation
15:33

Adenoviral Transduction of Naive CD4 T Cells to Study Treg Differentiation

Published on: August 13, 2013

Retroviral Transduction of Helper T Cells as a Genetic Approach to Study Mechanisms Controlling their Differentiation and Function
11:50

Retroviral Transduction of Helper T Cells as a Genetic Approach to Study Mechanisms Controlling their Differentiation and Function

Published on: November 4, 2016

Area of Science:

  • Immunology
  • Cell Biology
  • Molecular Biology

Background:

  • Regulatory T cells (Tregs) are critical for immune homeostasis, preventing autoimmunity and inflammation.
  • The role of phosphoinositide 3-kinase (PI3K) signaling in Treg function and development is complex and debated.
  • Conflicting data exists regarding whether PI3K pathway inhibition promotes or impairs Treg development and function.

Purpose of the Study:

  • To reconcile divergent findings on the role of PI3K signaling in Treg development and function.
  • To investigate the impact of PI3K and its downstream effectors (Akt, Foxo, mTOR) on Tregs.
  • To discuss the implications for immune health and therapeutic strategies.

Main Methods:

  • Literature review and synthesis of existing studies on PI3K signaling in Tregs.
  • Analysis of data concerning the downstream effectors Akt, Foxo, and mTOR in Treg biology.
  • Comparative analysis of studies with differing conclusions on PI3K pathway modulation.

Main Results:

  • The precise role of PI3K signaling in Tregs appears context-dependent, influencing both development and function.
  • Downstream effectors like Akt, Foxo, and mTOR exhibit differential regulation within Tregs.
  • Understanding these complex interactions is key to resolving discrepancies in the literature.

Conclusions:

  • Reconciliation of conflicting data suggests a nuanced role for PI3K signaling in Tregs.
  • Therapeutic targeting of the PI3K pathway in Tregs requires careful consideration of downstream effectors.
  • Further research is needed to fully elucidate PI3K pathway dynamics for potential therapeutic interventions in autoimmune diseases.