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Published on: October 17, 2017
Monocyte TREM-1 membrane expression in non-infectious inflammation
1Unit Cytokines & Inflammation, Institut Pasteur, 75015 Paris, France. jean-marc.cavaillon@pasteur.fr
Critical Care (London, England)
|June 13, 2009
Summary
Both sterile inflammation and severe infections share similar inflammatory events. Increased expression of triggering receptor expressed on myeloid cells 1 (TREM1) on immune cells is a key marker in both conditions.
Area of Science:
- Immunology
- Cell Biology
- Pathology
Background:
- Sterile inflammation and severe infections exhibit overlapping pathophysiological events.
- Molecular patterns, such as damage-associated molecular patterns (DAMPs) and pathogen-associated molecular patterns (PAMPs), initiate inflammatory responses.
- These patterns trigger the release of inflammatory mediators and alter cell surface receptor expression.
Purpose of the Study:
- To elucidate the shared molecular mechanisms underlying sterile and infectious inflammation.
- To identify common cellular markers indicative of both inflammatory states.
Main Methods:
- Analysis of inflammatory mediator release.
- Assessment of cell surface receptor expression, specifically focusing on myeloid cells.
- Comparative study of immune responses in sterile versus infectious inflammatory conditions.
Main Results:
- Both sterile and infectious inflammation involve similar inflammatory mediator release.
- A significant increase in the expression of triggering receptor expressed on myeloid cells 1 (TREM1) was observed on monocytes and neutrophils in both conditions.
- TREM1 expression serves as a common hallmark for both infectious and non-infectious inflammatory processes.
Conclusions:
- Infectious and sterile inflammation share common molecular triggers and cellular responses.
- Increased TREM1 expression on myeloid cells is a conserved marker for diverse inflammatory conditions.
- Targeting TREM1 may offer therapeutic potential for a broad range of inflammatory diseases.
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