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Running to stand still: BCR-like signaling suppresses type I IFN responses in pDC
Melissa K Swiecki1, Marco Colonna
1Department of Pathology and Immunology, Washington University School of Medicine, St Louis MO 63110, USA.
Insights
Plasmacytoid dendritic cells (pDCs) typically produce type I interferon (IFN). New research reveals a B cell receptor (BCR)-like pathway in pDCs that actually suppresses this crucial IFN production.
Area of Science:
- Immunology
- Cellular Biology
Background:
- Plasmacytoid dendritic cells (pDCs) are key producers of type I interferon (IFN).
- The regulatory pathways governing pDC type I IFN responses are not fully understood.
Purpose of the Study:
- To investigate novel signaling cascades that modulate type I IFN production in pDCs.
Main Methods:
- Analysis of B cell receptor (BCR)-like signaling pathways.
- Assessment of type I IFN production in pDCs.
Main Results:
- A BCR-like signaling cascade was identified in pDCs.
- This cascade was found to suppress type I IFN production.
Conclusions:
- pDCs possess an intrinsic regulatory mechanism involving BCR-like signaling.
- This pathway acts as a negative regulator of type I IFN production in pDCs.
Abstract:
Plasmacytoid dendritic cells (pDC) specialize in the secretion of type I interferon (IFN). Although multiple pathways that modulate type I IFN responses have been described they are inadequately defined. In this issue of the European Journal of Immunology, evidence for a B cell receptor (BCR)-like signaling cascade in pDC that suppresses type I IFN production is provided.
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