Mincle and human B cell function
Kazuhito Kawata1, Petr Illarionov, Guo-Xiang Yang
1Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis School of Medicine, Davis, 95616 CA, USA.
Journal of Autoimmunity
|June 16, 2012
Summary
Mincle, a C-type lectin receptor, is highly expressed on naive B cells. Its ligation reduces B cell antibody production, suggesting a role in human B cell immune responses.
Area of Science:
- Immunology
- Cell Biology
Background:
- C-type lectin receptors (CLRs) are crucial pattern recognition receptors involved in immune responses and autoimmunity.
- Mincle, a CLR expressed on various antigen-presenting cells, recognizes damaged cells and induces inflammatory cytokine production in macrophages.
- While Mincle's role in macrophage responses to fungal infections is established, its function in B cells remains unclear.
Purpose of the Study:
- To investigate the function of Mincle in human B cells.
- To analyze Mincle expression on different B cell subsets.
- To determine the effects of Mincle ligation on B cell cytokine and immunoglobulin synthesis.
Main Methods:
- Flow cytometry was used to assess Mincle expression on naive (CD27-CD19+) and memory (CD27+CD19+) B cells.
- B cells were stimulated with TLR9 ligand to induce Mincle expression.
- Mincle and TLR9 ligands were co-stimulated to analyze cytokine and immunoglobulin production.
Main Results:
- Mincle expression was significantly higher on naive B cells compared to memory B cells.
- TLR9 ligand stimulation increased Mincle expression on B cells.
- Co-stimulation of TLR9 and Mincle ligands decreased IgG and IgA production, with no significant changes in TNF-α, IL-6, IL-8, and IL-10.
Conclusions:
- Mincle is expressed on human B cells, with higher levels on naive B cells.
- Mincle ligation, in conjunction with TLR9 stimulation, modulates B cell immunoglobulin production.
- These findings identify Mincle as a significant factor in human B cell immune responses.
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