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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2015 pubmed 10 citations

Expression of the ATP-gated P2X7 Receptor on M Cells and Its Modulating Role in the Mucosal Immune Environment.

Kim. Sae-Hae SH; Lee. Ha-Yan HY; Jang. Yong-Suk YS

Key Findings

  • P2X7 receptors are present on intestinal M cells
  • Activating P2X7 with ATP or LL‑37 enhances mucosal immune responses
  • LL‑37 may act as a modulator of gut immunity via P2X7

Practical Outcomes

  • The study suggests LL‑37 could influence gut immune health, but it’s still basic research. Biohackers should view this as a mechanistic clue rather than a ready‑to‑use supplement protocol, and await further studies before trying any LL‑37‑based interventions.

Summary

Scientists found that a gut‑lining cell type called M cells has the ATP‑sensing P2X7 receptor, and that the antimicrobial peptide LL‑37 can activate this receptor to boost local immune activity. This is an early‑stage discovery showing a possible way the gut’s immune system can be tuned by molecules like LL‑37, but it doesn’t give dosing or practical tips yet.

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.

Study Information

Provider

pubmed

Year

2015

Date

2015-02-17T00:00:00.000Z

DOI

10.4110/in.2015.15.1.44

Citations

10

References

24