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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 1
2017 pubmed 18 citations

The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells.

Milhan. Noala Vicensoto Moreira NVM; de Barros. Patricia Pimentel PP; de Lima Zutin. Elis Andrade EA; de Oliveira. Felipe Eduardo FE; Camargo. Carlos Henrique Ribeiro CHR; Camargo. Samira Esteves Afonso SEA

Key Findings

  • 5‑10 µg/mL LL‑37 is non‑toxic to dental pulp stem cells
  • Higher dose (10 µg/mL) pauses cells in G0/G1 phase and boosts DSPP protein and gene expression
  • LL‑37 may aid the conversion of stem cells into odontoblast‑like cells

Practical Outcomes

  • For most DIY health enthusiasts this study isn’t directly usable, as it requires cell‑culture techniques. It does suggest that LL‑37 is safe at low micromolar levels and could be explored for dental tissue repair, but no simple dosing protocol for humans is provided.

Summary

LL-37, a natural antimicrobial peptide, was tested on human dental pulp stem cells in the lab. At 5‑10 µg/mL it didn’t kill the cells, actually helped them survive a bit more, and at the higher dose pushed them toward becoming tooth‑building cells by raising a protein called DSPP.

Abstract

This study evaluated the biocompatibility of 5 and 10 μg/mL LL-37 in vitro and its effect on the differentiation of human dental pulp stem cells (DPSCs) into odontoblast-like cells. Cell viability, genotoxicity, nitric oxide production, cell cycle, dentine sialophosphoprotein (DSPP) production, and DSPP gene expression. Concentrations of 5 and 10 μg/mL of LL-37 were not cytotoxic and generally increased cell viability, especially on the third day (P < .05). The tested concentrations did not induce genotoxicity (P < .05). LL-37 did not significantly alter nitrite production at either concentration. Cell cycle analysis revealed that 10 μg/mL of LL-37 arrested cells in G0/G1 (P < .05). The control group exhibited higher numbers of cells in other phases of the cell cycle (P < .05). The expression of the DSPP protein and gene was also higher in the 10 μg/mL of LL-37 group (P < .05). These results demonstrated that LL-37 was biocompatible at these concentrations and increased the number of viable cells, especially during the initial period. The 10 μg/mL concentration arrested the cell cycle and increased expression of the DSPP protein and gene, which indicates that this peptide contributes to odontoblastic differentiation.

Study Information

Provider

pubmed

Year

2017

Date

2017-10-21T00:00:00.000Z

DOI

10.1016/j.joen.2017.08.010

Citations

18

References

35