Molecular and cellular profiles of the resolution phase in a damage‐associated molecular pattern (DAMP)‐mediated peritonitis model and revelation of leukocyte persistence in peritoneal tissues. Issue 5 (21st January 2015)
- Record Type:
- Journal Article
- Title:
- Molecular and cellular profiles of the resolution phase in a damage‐associated molecular pattern (DAMP)‐mediated peritonitis model and revelation of leukocyte persistence in peritoneal tissues. Issue 5 (21st January 2015)
- Main Title:
- Molecular and cellular profiles of the resolution phase in a damage‐associated molecular pattern (DAMP)‐mediated peritonitis model and revelation of leukocyte persistence in peritoneal tissues
- Authors:
- Lastrucci, Claire
Baillif, Vincent
Behar, Annie
Saati, Talal Al
Dubourdeau, Marc
Maridonneau‐Parini, Isabelle
Cougoule, Céline - Abstract:
- ABSTRACT: Models of microbe‐elicited peritonitis have been invaluable to identify mechanisms underlying inflammation resolution, but whether resolution mechanisms differ from an inflammatory agent to another has not been determined. Thus, we analyzed the cellular and molecular components of the resolution phase of non‐microbe‐induced inflammation. In thioglycollate (TG)‐induced peritonitis, resolution started at 12 h ( T max ) and displayed a 22 h resolution interval (Ri ). During resolution, lipoxin A4, resolvin (Rv) D1 and RvD2, protectin D1 (PD1), and maresin 1 (MaR1) were transiently produced while RvD5 was continually generated. In addition, docosahexaenoic acid (DHA)‐derived mediators were produced to a higher extent than in microbial peritonitis. We also investigated leukocyte infiltration and clearance in peritoneal tissues surrounding the inflammatory site. In the omentum, resolution parameters, neutrophil apoptosis, and efferocytosis were similar to those of the peritoneal cavity. However, we noticed long‐term persistence of M2‐polarized macrophages and B‐lymphocytes in the omentum after TG administration, whereas zymosan injection caused M1/M2‐macrophage and T‐lymphocyte persistence regardless of the magnitude of the inflammatory response. Our study indicates that some aspects of resolution are shaped in a stimulus‐specific manner, and it ultimately argues that the tissues surrounding the inflammatory site must also be considered to address the inflammatoryABSTRACT: Models of microbe‐elicited peritonitis have been invaluable to identify mechanisms underlying inflammation resolution, but whether resolution mechanisms differ from an inflammatory agent to another has not been determined. Thus, we analyzed the cellular and molecular components of the resolution phase of non‐microbe‐induced inflammation. In thioglycollate (TG)‐induced peritonitis, resolution started at 12 h ( T max ) and displayed a 22 h resolution interval (Ri ). During resolution, lipoxin A4, resolvin (Rv) D1 and RvD2, protectin D1 (PD1), and maresin 1 (MaR1) were transiently produced while RvD5 was continually generated. In addition, docosahexaenoic acid (DHA)‐derived mediators were produced to a higher extent than in microbial peritonitis. We also investigated leukocyte infiltration and clearance in peritoneal tissues surrounding the inflammatory site. In the omentum, resolution parameters, neutrophil apoptosis, and efferocytosis were similar to those of the peritoneal cavity. However, we noticed long‐term persistence of M2‐polarized macrophages and B‐lymphocytes in the omentum after TG administration, whereas zymosan injection caused M1/M2‐macrophage and T‐lymphocyte persistence regardless of the magnitude of the inflammatory response. Our study indicates that some aspects of resolution are shaped in a stimulus‐specific manner, and it ultimately argues that the tissues surrounding the inflammatory site must also be considered to address the inflammatory response globally.—Lastrucci, C., Baillif, V., Behar, A., Al Saati, T., Dubourdeau, M., Maridonneau‐Parini, I., Cougoule, C. Molecular and cellular profiles of the resolution phase in a damage‐associated molecular pattern (DAMP)‐mediated peritonitis model and revelation of leukocyte persistence in peritoneal tissues. FASEB J. 29, 1914‐1929 (2015). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 29:Issue 5(2015)
- Journal:
- FASEB journal
- Issue:
- Volume 29:Issue 5(2015)
- Issue Display:
- Volume 29, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 5
- Issue Sort Value:
- 2015-0029-0005-0000
- Page Start:
- 1914
- Page End:
- 1929
- Publication Date:
- 2015-01-21
- Subjects:
- bioactive lipid mediators -- omentum -- macrophage polarization
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.14-259341 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14815.xml