Dissecting the relationship between antimicrobial peptides and mesenchymal stem cells.
Silva-Carvalho. Amandda Évelin AÉ; Cardoso. Marlon Henrique MH; Alencar-Silva. Thuany T; Bogéa. Gabriela Muller Reche GMR; Carvalho. Juliana Lott JL; Franco. Octávio Luiz OL; Saldanha-Araujo. Felipe F
Key Findings
- Mesenchymal stem cells (MSCs) produce LL‑37 along with other antimicrobial peptides.
- LL‑37 not only kills microbes but also influences MSC proliferation, migration, and regeneration.
- Combining MSCs with antimicrobial peptides like LL‑37 is proposed as a future therapeutic strategy.
Practical Outcomes
- For biohackers, the takeaway is that LL‑37 may have dual roles—antimicrobial and stem‑cell‑modulating—but there’s no ready‑to‑use supplement protocol yet. More research is needed before trying LL‑37 for longevity or performance benefits.
Summary
This paper reviews how stem cells naturally make the antimicrobial peptide LL‑37 (and others) and how that peptide can also affect the stem cells themselves, boosting their growth and movement. It suggests that mixing stem cells with LL‑37 could improve treatments against infections and aid tissue repair, but it doesn’t give specific dosing or protocols for everyday use.
Abstract
Among the various biological properties presented by Mesenchymal Stem Cells (MSCs), their ability to control the immune response and fight pathogen infection through the production of antimicrobial peptides (AMPs) have been the subject of intense research in recent years. AMPs secreted by MSCs exhibit activity against a wide range of microorganisms, including bacteria, fungi, yeasts, and viruses. The main AMPs produced by these cells are hepcidin, cathelicidin LL-37, and β-defensin-2. In addition to acting against pathogens, those AMPs have also been shown to interact with MSCs to modulate MSC proliferation, migration, and regeneration, indicating that such peptides exert a more diverse biological effect than initially thought. In the present review, we discuss the production of AMPs by MSCs, revise the multiple functions of these peptides, including their influence over MSCs, and present an overview of clinical situations in which the antimicrobial properties of MSCs may be explored for therapy. Finally, we discuss possibilities of combining MSCs and AMPs to generate improved therapeutic strategies.
Study Information
pubmed
2021
2021-10-09T00:00:00.000Z
10.1016/j.pharmthera.2021.108021
31
222