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Related Concept Videos

Overview of Exosomes01:36

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Exosomes are stable, lipid bilayer-enclosed vesicles capable of crossing biological barriers. They can carry a wide range of molecules required for intercellular communication. Once exosomes are released from the cell where they originated, they enter a recipient cell through various pathways such as fusion, receptor-mediated endocytosis, macropinocytosis, and phagocytosis.
Stahl et al. discovered exosomes in 1983, but the exosomes were initially considered waste products released from the...
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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.
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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.
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Exocytosis00:50

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Exocytosis is a process that releases molecules outside the cell. Like other bulk transport mechanisms, exocytosis requires energy.
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Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
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Isolation and Characterization of RNA-Containing Exosomes
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Biogenesis and Function of T Cell-Derived Exosomes.

Leandro N Ventimiglia1, Miguel A Alonso1

  • 1Cell Biology and Immunology, Centro de Biología Molecular "Severo Ochoa," Consejo Superior de Investigaciones Científicas and Universidad Autónoma de Madrid Madrid, Spain.

Frontiers in Cell and Developmental Biology
|September 2, 2016
PubMed
Summary

T-cell exosomes carry bioactive molecules to modulate other immune cells. Understanding exosome biogenesis in T cells, focusing on protein sorting, reveals therapeutic targets for immune response modulation.

Keywords:
ESCRT complexMAL proteincondensed membranesexosomesmultivesicular endosomestetraspanins

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Area of Science:

  • Immunology
  • Cell Biology
  • Extracellular Vesicles

Background:

  • Exosomes are extracellular vesicles originating from endosomes, involved in intercellular communication.
  • They transport bioactive molecules like lipids, proteins, and nucleic acids, influencing distant cells.
  • Exosomal cargo varies by cell type, necessitating understanding of their biogenesis and composition.

Purpose of the Study:

  • To review advances in T-cell exosome function and biogenesis.
  • To focus on protein sorting mechanisms within multivesicular endosomes in T cells.
  • To identify potential therapeutic targets for modulating immune responses via T-cell exosomes.

Main Methods:

  • Review of current literature on T-cell exosome biogenesis and function.
  • Focus on protein sorting mechanisms at multivesicular endosomes.
  • Identification of key molecules involved in T-cell exosome production.

Main Results:

  • T-cell exosomes can modulate the activity of other immune cells, including T-cell subsets.
  • Ceramide, tetraspanins, and MAL are identified as crucial for T-cell exosome biogenesis.
  • These molecules represent potential targets for therapeutic manipulation of exosome production.

Conclusions:

  • T-cell exosome biogenesis and protein sorting are critical for their immunomodulatory functions.
  • Targeting molecules like ceramide, tetraspanins, and MAL offers a strategy for therapeutic intervention.
  • Further research into T-cell exosome mechanisms can advance immunomodulatory therapies.