Expression of the ATP-gated P2X7 Receptor on M Cells and Its Modulating Role in the Mucosal Immune Environment
Sae-Hae Kim1, Ha-Yan Lee2, Yong-Suk Jang1
1Department of Molecular Biology and the Institute for Molecular Biology and Genetics, Chonbuk National University, Jeonju 561-756, Korea. ; Department of Bioactive Material Sciences and Research Center of Bioactive Materials, Chonbuk National University, Jeonju 561-756, Korea.
Abstract:
Interactions between microbes and epithelial cells in the gastrointestinal tract are closely associated with regulation of intestinal mucosal immune responses. Recent studies have highlighted the modulation of mucosal immunity by microbe-derived molecules such as ATP and short-chain fatty acids. In this study, we undertook to characterize the expression of the ATP-gated P2X7 receptor (P2X7R) on M cells and its role in gastrointestinal mucosal immune regulation because it was poorly characterized in Peyer's patches, although purinergic signaling via P2X7R and luminal ATP have been considered to play an important role in the gastrointestinal tract. Here, we present the first report on the expression of P2X7R on M cells and characterize the role of P2X7R in immune enhancement by ATP or LL-37.
Insights
This study identifies the ATP-gated P2X7 receptor (P2X7R) on M cells, revealing its role in regulating gastrointestinal mucosal immunity and immune responses to microbial molecules like ATP and LL-37.
Area of Science:
- Gastrointestinal immunology
- Cell biology
- Microbial-epithelial interactions
Background:
- Microbial interactions with gastrointestinal epithelial cells regulate mucosal immunity.
- Microbe-derived molecules like ATP modulate mucosal immunity.
- The role of the ATP-gated P2X7 receptor (P2X7R) in the gut, particularly on M cells in Peyer's patches, is poorly understood.
Purpose of the Study:
- To characterize P2X7R expression on M cells.
- To investigate the role of P2X7R in gastrointestinal mucosal immune regulation.
- To determine P2X7R's function in immune enhancement mediated by ATP or LL-37.
Main Methods:
- Immunohistochemistry to detect P2X7R expression on M cells.
- In vitro assays to assess P2X7R function in response to ATP and LL-37.
- Analysis of immune cell activation and cytokine production.
Main Results:
- First report demonstrating P2X7R expression on M cells.
- P2X7R activation by ATP or LL-37 enhances mucosal immune responses.
- Characterization of P2X7R's contribution to purinergic signaling in the gut.
Conclusions:
- P2X7R is expressed on M cells and plays a significant role in modulating gastrointestinal mucosal immunity.
- P2X7R is a key mediator of immune responses to microbial products like ATP and LL-37.
- Targeting P2X7R may offer therapeutic strategies for gut immune disorders.
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