The immune modulatory peptide FhHDM‐1 secreted by the helminth Fasciola hepatica prevents NLRP3 inflammasome activation by inhibiting endolysosomal acidification in macrophages. Issue 1 (28th September 2016)
- Record Type:
- Journal Article
- Title:
- The immune modulatory peptide FhHDM‐1 secreted by the helminth Fasciola hepatica prevents NLRP3 inflammasome activation by inhibiting endolysosomal acidification in macrophages. Issue 1 (28th September 2016)
- Main Title:
- The immune modulatory peptide FhHDM‐1 secreted by the helminth Fasciola hepatica prevents NLRP3 inflammasome activation by inhibiting endolysosomal acidification in macrophages
- Authors:
- Alvarado, Raquel
To, Joyce
Lund, Maria E.
Pinar, Anita
Mansell, Ashley
Robinson, Mark W.
O'Brien, Bronwyn A.
Dalton, John P.
Donnelly, Sheila - Abstract:
- Abstract : The NLRP3 inflammasome is a multimeric protein complex that controls the production of IL‐1β, a cytokine that influences the development of both innate and adaptive immune responses. Helminth parasites secrete molecules that interact with innate immune cells, modulating their activity to ultimately determine the phenotype of differentiated T cells, thus creating an immune environment that is conducive to sustaining chronic infection. We show that one of these molecules, FhHDM‐1, a cathelicidin‐like peptide secreted by the helminth parasite, Fasciola hepatica, inhibits the activation of the NLRP3 inflammasome resulting in reduced secretion of IL‐1β by macrophages. FhHDM‐1 had no effect on the synthesis of pro‐IL‐1β. Rather, the inhibitory effect was associatedwith the capacity of the peptide to prevent acidification of the endolysosome. The activation of cathepsin B protease by lysosomal destabilization was prevented in FhHDM‐1‐treated macrophages. By contrast, peptide derivatives of FhHDM‐1 that did not alter the lysosomal pH did not inhibit secretion of IL‐1β. Wepropose a novel immunemodulatory strategy usedby F. hepatica, whereby secretion of the FhHDM‐1 peptide impairs the activation of NLRP3 by lysosomal cathepsin B protease, which prevents the downstream production of IL‐1β and the development of protective T helper 1 type immune responses that are detrimental to parasite survival.—Alvarado, R., To, J., Lund, M. E., Pinar, A., Mansell, A., Robinson, M. W.,Abstract : The NLRP3 inflammasome is a multimeric protein complex that controls the production of IL‐1β, a cytokine that influences the development of both innate and adaptive immune responses. Helminth parasites secrete molecules that interact with innate immune cells, modulating their activity to ultimately determine the phenotype of differentiated T cells, thus creating an immune environment that is conducive to sustaining chronic infection. We show that one of these molecules, FhHDM‐1, a cathelicidin‐like peptide secreted by the helminth parasite, Fasciola hepatica, inhibits the activation of the NLRP3 inflammasome resulting in reduced secretion of IL‐1β by macrophages. FhHDM‐1 had no effect on the synthesis of pro‐IL‐1β. Rather, the inhibitory effect was associatedwith the capacity of the peptide to prevent acidification of the endolysosome. The activation of cathepsin B protease by lysosomal destabilization was prevented in FhHDM‐1‐treated macrophages. By contrast, peptide derivatives of FhHDM‐1 that did not alter the lysosomal pH did not inhibit secretion of IL‐1β. Wepropose a novel immunemodulatory strategy usedby F. hepatica, whereby secretion of the FhHDM‐1 peptide impairs the activation of NLRP3 by lysosomal cathepsin B protease, which prevents the downstream production of IL‐1β and the development of protective T helper 1 type immune responses that are detrimental to parasite survival.—Alvarado, R., To, J., Lund, M. E., Pinar, A., Mansell, A., Robinson, M. W., O'Brien, B. A., Dalton, J. P., Donnelly, S. The immune modulatory peptide FhHDM‐1 secreted by the helminth Fasciola hepatica prevents NLRP3 inflammasome activation by inhibiting endolysosomal acidification in macrophages. FASEB J. 31, 85–95 (2017) www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 31:Issue 1(2017)
- Journal:
- FASEB journal
- Issue:
- Volume 31:Issue 1(2017)
- Issue Display:
- Volume 31, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 31
- Issue:
- 1
- Issue Sort Value:
- 2017-0031-0001-0000
- Page Start:
- 85
- Page End:
- 95
- Publication Date:
- 2016-09-28
- Subjects:
- trematode -- liver fluke -- IL‐1b -- lysosome
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201500093r ↗
- 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:
- 13227.xml