Neutrophil Extracellular Trap Induced Dendritic Cell Activation Leads to Th1 Polarization in Type 1 Diabetes
Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
32346380
PubMed Central
PMC7172866
DOI
10.3389/fimmu.2020.00661
Knihovny.cz E-zdroje
- Klíčová slova
- NET, autoimmunity, innate immunity, monocyte-derived dendritic cells, netosis, neutrophils, type 1 diabetes,
- MeSH
- buněčná diferenciace MeSH
- dendritické buňky imunologie MeSH
- diabetes mellitus 1. typu imunologie MeSH
- dítě MeSH
- dospělí MeSH
- extracelulární pasti imunologie MeSH
- interferon gama metabolismus MeSH
- kultivované buňky MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- neutrofily imunologie MeSH
- přirozená imunita MeSH
- regulace genové exprese MeSH
- rovnováha Th1-Th2 MeSH
- Th1 buňky imunologie MeSH
- transformující růstový faktor beta metabolismus MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- interferon gama MeSH
- transformující růstový faktor beta MeSH
Neutrophils releasing neutrophil extracellular traps (NETs) infiltrate the pancreas prior to type 1 diabetes (T1D) onset; however, the precise nature of their contribution to disease remains poorly defined. To examine how NETs affect immune functions in T1D, we investigated NET composition and their effect on dendritic cells (DCs) and T lymphocytes in T1D children. We showed that T1D patient NET composition differs substantially from that of healthy donors and that the presence of T1D-NETs in a mixed peripheral blood mononuclear cell culture caused a strong shift toward IFNγ-producing T lymphocytes, mediated through activation of innate immunity cells in T1D samples. Importantly, in a monocyte-derived DC (moDC) culture, NETs induced cytokine production, phenotypic change and IFNγ-producing T cells only in samples from T1D patients but not in those from healthy donors. RNA-seq analysis revealed that T1D-NETs presence causes TGFβ downregulation and IFNα upregulation and creates pro-T1D signature in healthy moDCs.
Christian Albrecht University of Kiel Kiel Germany
Institute of Clinical Molecular Biology University Hospital in Schleswig Holstein Kiel Germany
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