Apoptotic-cell-derived membrane microparticles and IFN-α induce an inflammatory immune response.
J Cell Sci
; 128(14): 2443-53, 2015 Jul 15.
Article
en En
| MEDLINE
| ID: mdl-26034070
ABSTRACT
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.
Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Interferón-alfa
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Apoptosis
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Micropartículas Derivadas de Células
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Lupus Eritematoso Sistémico
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Macrófagos
Límite:
Female
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Humans
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Male
Idioma:
En
Revista:
J Cell Sci
Año:
2015
Tipo del documento:
Article
País de afiliación:
Alemania