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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2025 pubmed 3 citations

Temporal dynamics of the interstitial fluid proteome in human skeletal muscle following exhaustive exercise.

Stocks. Ben B; Quesada. Julia Prats JP; Mozzicato. Anthony M AM; Jacob. Carolina C; Jensen. Simone S; MacGregor. Kirstin A KA; Bangsbo. Jens J; Zierath. Juleen R JR; Hostrup. Morten M; Deshmukh. Atul S AS

Key Findings

  • Exhaustive exercise increases CAMP/LL‑37 levels in muscle interstitial fluid
  • LL‑37 treatment enlarges C2C12 muscle cells in vitro
  • LL‑37 activates PI3K/AKT, MAPK, and mTOR pathways linked to muscle growth

Practical Outcomes

  • LL‑37 looks promising as a muscle‑growth enhancer, but currently it’s only proven in cell culture. Biohackers should treat it as a research target rather than a ready‑to‑use supplement until human studies, dosing guidelines, and safety data emerge.

Summary

After a hard workout, a natural peptide called LL‑37 (derived from CAMP) rises in the fluid around muscle fibers. In lab tests, adding LL‑37 to muscle cells made them grow bigger and turned on key growth pathways. The study shows LL‑37 might help muscle building, but it’s only been tested in cells, not people, and no dosing or safety info is available yet.

Abstract

The skeletal muscle interstitial space is the extracellular region around myofibers and mediates cross-talk between resident cell types. We applied a proteomic workflow to characterize the human skeletal muscle interstitial fluid proteome at rest and in response to exercise. Following exhaustive exercise, markers of skeletal muscle damage accumulate in the interstitial space followed by the appearance of immune cell-derived proteins. Among the proteins up-regulated after exercise, we identified cathelicidin-related antimicrobial peptide (CAMP) as a bioactive molecule regulating muscle fiber development. Treatment with the bioactive peptide derivative of CAMP (LL-37) resulted in the growth of larger C2C12 skeletal muscle myotubes. Phosphoproteomics revealed that LL-37 activated pathways central to muscle growth and proliferation, including phosphatidylinositol 3-kinase, AKT serine/threonine kinase 1, mitogen-activated protein kinases, and mammalian target of rapamycin. Our findings provide a proof of concept that the interstitial fluid proteome is quantifiable via microdialysis sampling in vivo. These data highlight the importance of cellular communication in the adaptive response to exercise.

Study Information

Provider

pubmed

Year

2025

Date

2025-01-31T00:00:00.000Z

DOI

10.1126/sciadv.adp8608

Citations

3

References

44