Apoptotic-cell-derived membrane microparticles and IFN-α induce an inflammatory immune response

A Section a dysregulation in the clearance of apoptotic material is considered a major pathogenetic factor for the emergence of autoimmune diseases. Apoptotic-cell-derived membrane microparticles (AdMPs), which are released from the cell surface during apoptosis, have been implicated in the pathogen...

Full description

Saved in:
Bibliographic Details
Main Authors: Nießen, Anna (Author) , Heyder, Petra (Author) , Krienke, Stefan (Author) , Blank, Norbert (Author) , Tykocinski, Lars-Oliver (Author) , Lorenz, Hanns-Martin (Author) , Schiller, Martin (Author)
Format: Article (Journal)
Language:English
Published: 15 July 2015
In: Journal of cell science
Year: 2015, Volume: 128, Issue: 14, Pages: 2443-2453
ISSN:1477-9137
DOI:10.1242/jcs.162735
Online Access:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1242/jcs.162735
Verlag, kostenfrei, Volltext: http://jcs.biologists.org/content/128/14/2443
Get full text
Author Notes:Anna Niessen, Petra Heyder, Stefan Krienke, Norbert Blank, Lars-Oliver Tykocinski, Hanns-Martin Lorenz, Martin Schiller
Description
Summary:A Section a dysregulation in the clearance of apoptotic material is considered a major pathogenetic factor for the emergence of autoimmune diseases. Apoptotic-cell-derived membrane microparticles (AdMPs), which are released from the cell surface during apoptosis, have been implicated in the pathogenesis of autoimmunity. Also of importance are cytokines, such as interferon-α (IFN-α), which is known to be a major player in patients with systemic lupus erythematosus (SLE). This study investigates the combined effect of AdMPs and IFN-α on professional phagocytes. In the presence of IFN-α, phagocytosis of AdMPs by human monocytes was significantly increased in a dose-dependent manner. The combination of AdMPs and raised IFN-α concentrations resulted in an increase in the secretion of pro-inflammatory cytokines and an upregulation of surface molecule expression involved in antigen uptake. In addition, macrophage polarisation was shifted towards a more inflammatory type of cell. The synergism between IFN-α and AdMPs seemed to be mediated by an upregulation of phosphorylated STAT1. Our results indicate that IFN-α, together with AdMPs, amplify the initiation and maintenance of inflammation. This mechanism might especially play a crucial role in disorders with a defective clearance of apoptotic material.
Item Description:Gesehen am 23.02.2017
Physical Description:Online Resource
ISSN:1477-9137
DOI:10.1242/jcs.162735