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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2024 pubmed 40 citations

LL-37: Structures, Antimicrobial Activity, and Influence on Amyloid-Related Diseases.

Bhattacharjya. Surajit S; Zhang. Zhizhuo Z; Ramamoorthy. Ayyalusamy A

Key Findings

  • LL-37 is the only human cathelicidin peptide and is found in many tissues, from skin to gut.
  • Beyond killing microbes, LL-37 can modulate inflammation, attract immune cells, and promote wound healing.
  • Derived fragments of LL-37 show anti‑cancer and anti‑amyloid (protein‑clumping) activities, suggesting broader therapeutic potential.

Practical Outcomes

  • For now, the main takeaway is that LL‑37 is a promising template for future antimicrobial and disease‑modifying drugs, but there are no validated dosing guidelines or ready‑to‑use protocols for self‑experimenters. Keep an eye on emerging LL‑37‑based supplements or topical products, and consider the peptide’s safety profile before any DIY use.

Summary

LL-37 is a natural 37‑amino‑acid peptide that helps our bodies fight infections, calm inflammation, attract immune cells, heal wounds, and may even protect against cancer and harmful protein clumps linked to diseases like Alzheimer’s. Scientists are studying its shape and how it works so they can design new drugs based on it, but the review doesn’t give specific ways to use LL‑37 right now.

Abstract

Antimicrobial peptides (AMPs), as well as host defense peptides (HDPs), constitute the first line of defense as part of the innate immune system. Humans are known to express antimicrobial precursor proteins, which are further processed to generate AMPs, including several types of α/β defensins, histatins, and cathelicidin-derived AMPs like LL37. The broad-spectrum activity of AMPs is crucial to defend against infections caused by pathogenic bacteria, viruses, fungi, and parasites. The emergence of multi-drug resistant pathogenic bacteria is of global concern for public health. The prospects of targeting antibiotic-resistant strains of bacteria with AMPs are of high significance for developing new generations of antimicrobial agents. The 37-residue long LL37, the only cathelicidin family of AMP in humans, has been the major focus for the past few decades of research. The host defense activity of LL37 is likely underscored by its expression throughout the body, spanning from the epithelial cells of various organs-testis, skin, respiratory tract, and gastrointestinal tract-to immune cells. Remarkably, apart from canonical direct killing of pathogenic organisms, LL37 exerts several other host defense activities, including inflammatory response modulation, chemo-attraction, and wound healing and closure at the infected sites. In addition, LL37 and its derived peptides are bestowed with anti-cancer and anti-amyloidogenic properties. In this review article, we aim to develop integrative, mechanistic insight into LL37 and its derived peptides, based on the known biophysical, structural, and functional studies in recent years. We believe that this review will pave the way for future research on the structures, biochemical and biophysical properties, and design of novel LL37-based molecules.

Study Information

Provider

pubmed

Year

2024

Date

2024-03-08T00:00:00.000Z

DOI

10.3390/biom14030320

Citations

40

References

262