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Related Concept Videos

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...
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...

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Related Experiment Video

Updated: May 13, 2026

An Adipocyte Cell Culture Model to Study the Impact of Protein and Micro-RNA Modulation on Adipocyte Function
09:20

An Adipocyte Cell Culture Model to Study the Impact of Protein and Micro-RNA Modulation on Adipocyte Function

Published on: May 4, 2021

Adipocyte-derived lipids modulate CD4+ T-cell function.

Andreea Ioan-Facsinay1, Joanneke C Kwekkeboom, Sanne Westhoff

  • 1Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands. A.Ioan@lumc.nl

European Journal of Immunology
|March 19, 2013
PubMed
Summary
This summary is machine-generated.

Adipose tissue immune cells, like Interferon-gamma (IFN-γ) CD4(+) T cells, are influenced by adipocytes. Adipocytes release lipids, particularly free fatty acids, that enhance T-cell proliferation and cytokine production.

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Isolation of Adipose Tissue Immune Cells
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Isolation, Expansion, and Adipogenic Induction of CD34+CD31+ Endothelial Cells from Human Omental and Subcutaneous Adipose Tissue

Published on: July 17, 2018

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Last Updated: May 13, 2026

An Adipocyte Cell Culture Model to Study the Impact of Protein and Micro-RNA Modulation on Adipocyte Function
09:20

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Published on: May 4, 2021

Isolation of Adipose Tissue Immune Cells
07:09

Isolation of Adipose Tissue Immune Cells

Published on: May 22, 2013

Isolation, Expansion, and Adipogenic Induction of CD34+CD31+ Endothelial Cells from Human Omental and Subcutaneous Adipose Tissue
10:28

Isolation, Expansion, and Adipogenic Induction of CD34+CD31+ Endothelial Cells from Human Omental and Subcutaneous Adipose Tissue

Published on: July 17, 2018

Area of Science:

  • Immunology
  • Cell Biology
  • Metabolic Research

Background:

  • Adipose tissue harbors diverse immune cells with phenotypes varying by adiposity.
  • IFN-γ(+) CD4(+) T cells are found in higher concentrations in human adipose tissue than in blood.

Purpose of the Study:

  • To investigate how human adipocytes modulate CD4(+) T-cell cytokine production and proliferation.
  • To identify the specific mediators released by adipocytes that affect T-cell function.

Main Methods:

  • Co-culture experiments with activated CD4(+) T cells and adipocytes.
  • Transwell assays and analysis of adipocyte-conditioned medium (ACM).
  • Fractionation of ACM to isolate lipid and protein components, followed by fatty acid analysis.

Main Results:

  • Adipocytes significantly increase IFN-γ production by activated CD4(+) T cells via soluble mediators.
  • ACM enhances CD4(+) T-cell proliferation upon activation.
  • The proliferation-enhancing effect is primarily attributed to the lipid fraction of ACM, specifically free fatty acids.

Conclusions:

  • Adipocytes modulate CD4(+) T-cell function, including proliferation and cytokine production, through lipid secretion.
  • Free fatty acids are key mediators in this process, potentially contributing to T-cell accumulation in adipose tissue.