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Updated: Jul 7, 2026

Legionella pneumophila Outer Membrane Vesicles: Isolation and Analysis of Their Pro-inflammatory Potential on Macrophages
Published on: February 22, 2017
Exosomes secreted by bacterially infected macrophages are proinflammatory
Helen C O'Neill1, Ben J C Quah
1School of Biochemistry and Molecular Biology, College of Science, The Australian National University, Canberra, ACT 0200, Australia. Helen.ONeill@anu.edu.au
Abstract:
Exosomes are small vesicles that are secreted from cells. They are derived from multivesicular endosomes that fuse with the plasma membrane, thereby releasing their internal vesicles into the extracellular environment. Exosomes from antigen-presenting cells contain a range of immunostimulatory molecules that activate T cells, which suggests that they may have an important role in the propagation of immune responses. Of considerable interest is the finding that exosomes derived from bacterially infected macrophages carry bacterial coat components and use these to stimulate bystander macrophages and neutrophils to secrete proinflammatory mediators, including tumor necrosis factor-alpha, the chemokine regulated upon activation, normal T cell-expressed and -secreted (RANTES, also known as CCL5), and inducible nitric oxide synthase. Here, we address these studies in relation to other findings on dendritic cell-derived exosomes that are also powerful immunoregulators.
Insights
Exosomes secreted by infected macrophages carry bacterial components, activating other immune cells to release inflammatory signals. These findings highlight exosomes
Area of Science:
- Cell Biology
- Immunology
- Extracellular Vesicles
Background:
- Exosomes are small extracellular vesicles released from cells via endosomal pathways.
- These vesicles contain various molecules, including immunostimulatory components.
- Exosomes play a role in intercellular communication and immune response modulation.
Purpose of the Study:
- To investigate the immunoregulatory functions of exosomes, particularly those derived from infected macrophages.
- To explore how bacterial components on exosomes influence immune cell activation.
- To relate these findings to the known immunomodulatory effects of dendritic cell-derived exosomes.
Main Methods:
- Analysis of exosome composition from infected macrophages.
- Assessment of exosome-mediated stimulation of bystander immune cells (macrophages, neutrophils).
- Measurement of secreted proinflammatory mediators.
Main Results:
- Exosomes from bacterially infected macrophages carry bacterial coat components.
- These exosomes stimulate macrophages and neutrophils to secrete proinflammatory mediators.
- Key mediators include tumor necrosis factor-alpha, RANTES (CCL5), and inducible nitric oxide synthase.
Conclusions:
- Exosomes derived from infected macrophages act as potent immune mediators.
- Bacterial components on exosomes are crucial for activating bystander immune cells.
- Exosomes are significant regulators of innate and adaptive immune responses.
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