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The expression of membrane-bound CD14 renders mouse B-1 cells susceptible to LPS
T Sugiyama1, N Koide, D Chakravortty
1Department of Microbiology and Immunology, and Division of Bacterial Toxin, Research Center for Infectious Disease, Aichi Medical University, Nagakute, Aichi, Japan. sugiyama@aichi-med-u.ac.jp
Abstract:
The surface expression of CD14 on mouse B-1 cells and its role on their response to lipopolysaccharide (LPS) were studied by using the murine TH2.52 B-1 cell line and peritoneal B-1 cells. TH2.52 cells with the B-1 phenotype were found to express membrane-bound CD14. Furthermore, CD14 was expressed on physiological peritoneal CD5+ B-1 cells. The stimulation of CD14-expressing TH2.52 cells with a low concentration of LPS resulted in the activation of nuclear factor (NF)-B and a mitogen-activated protein kinase (MAPK). The LPS-induced NF-B and MAPK activation was markedly inhibited by anti-CD14 antibody. These results suggest that B-1 cells may respond to LPS via membrane-bound CD14.
Insights
Mouse B-1 cells express CD14, a molecule crucial for their response to lipopolysaccharide (LPS). This suggests B-1 cells utilize membrane-bound CD14 to detect and react to LPS.
Area of Science:
- Immunology
- Cell Biology
Background:
- B-1 cells are a distinct subset of lymphocytes with unique immune functions.
- Lipopolysaccharide (LPS) is a potent activator of the innate immune system, primarily recognized by Toll-like receptor 4 (TLR4).
- CD14 is a pattern recognition receptor involved in LPS sensing.
Purpose of the Study:
- To investigate the surface expression of CD14 on mouse B-1 cells.
- To determine the role of CD14 in the response of B-1 cells to LPS.
Main Methods:
- Utilized the murine TH2.52 B-1 cell line and primary peritoneal B-1 cells.
- Assessed CD14 surface expression via flow cytometry.
- Stimulated cells with LPS and measured activation of nuclear factor (NF)-κB and mitogen-activated protein kinase (MAPK) pathways.
- Investigated the effect of anti-CD14 antibody on LPS-induced signaling.
Main Results:
- Both the TH2.52 B-1 cell line and primary peritoneal CD5+ B-1 cells expressed membrane-bound CD14.
- LPS stimulation of CD14-expressing TH2.52 cells induced NF-κB and MAPK activation.
- Anti-CD14 antibody significantly inhibited LPS-induced NF-κB and MAPK activation.
Conclusions:
- Mouse B-1 cells express CD14 on their surface.
- Membrane-bound CD14 plays a significant role in mediating the activation of B-1 cells by LPS.
- These findings suggest a novel mechanism for B-1 cell recognition of LPS through CD14.