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Published on: September 15, 2017
Microparticles as mediators of cellular cross-talk in inflammatory disease
Jörg H W Distler1, Lars C Huber, Steffen Gay
1Department of Internal Medicine 3, University of Erlangen, Erlangen, Germany.
Abstract:
Microparticles are a heterogeneous population of membrane-coated vesicles which can be released from virtually all cell types during activation or apoptosis. Release occurs from the cell surface in an exogenous budding process involving local rearrangement of the cytoskeleton. Given their origin, these particles can be identified by staining for cell surface markers and annexin V. As shown in in vitro studies, microparticles may represent a novel subcellular element for intercellular communication in inflammation. Thus, microparticles can transfer chemokine receptors and arachidonic acid between cells, activate complement, promote leukocyte rolling and stimulate the release of pro-inflammatory mediators. Under certain conditions, however, microparticles may also exert anti-inflammatory properties by inducing immune cell apoptosis and the production of anti-inflammatory mediators. Microparticles may play an important role in the pathogenesis of rheumatologic diseases as evidenced by their elevation in diseases such as systemic sclerosis (SSc), systemic vasculitis and antiphospholipid antibody syndrome and correlation with clinical events. A role in inflammatory arthritis is suggested by the finding that leukocyte-derived microparticles induce the production of matrix metalloproteinases and cytokines by synovial fibroblasts. Together, these findings point to novel signaling pathways of cellular cross-talk that may operate along the spectrum of soluble cytokines and mediators of direct cell-cell contact.
Insights
Microparticles, small cell-derived vesicles, are key in intercellular communication during inflammation. They can promote or reduce inflammation and are implicated in rheumatologic diseases, offering insights into novel cellular signaling pathways.
Area of Science:
- Cell Biology
- Immunology
- Biochemistry
Background:
- Microparticles are vesicles released from cells during activation or apoptosis.
- They bud from the cell surface and can be identified by cell surface markers and annexin V.
- Microparticles play a role in intercellular communication, particularly in inflammation.
Purpose of the Study:
- To explore the role of microparticles in intercellular communication.
- To investigate the pro- and anti-inflammatory properties of microparticles.
- To examine the involvement of microparticles in rheumatologic diseases.
Main Methods:
- In vitro studies analyzing microparticle release and function.
- Staining for cell surface markers and annexin V to identify microparticles.
- Observational studies in patients with rheumatologic diseases.
Main Results:
- Microparticles transfer molecules like chemokine receptors and arachidonic acid between cells.
- They can activate complement, promote leukocyte rolling, and stimulate pro-inflammatory mediator release.
- Microparticles can also induce immune cell apoptosis and anti-inflammatory mediator production.
- Elevated microparticle levels are observed in systemic sclerosis, vasculitis, and antiphospholipid antibody syndrome.
- Leukocyte-derived microparticles stimulate cytokine and matrix metalloproteinase production by synovial fibroblasts.
Conclusions:
- Microparticles are versatile mediators of intercellular communication with both pro- and anti-inflammatory effects.
- They are implicated in the pathogenesis of rheumatologic diseases.
- Microparticles represent novel signaling pathways in cellular cross-talk, bridging cytokine signaling and direct cell-cell contact.
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