# The antibacterial effect of human adipose-derived stem cells on LL-37-resistant bacteria

**Authors:** Parisa Afzal Haghjoo, Ali Mojtahedi, Malek Moien Ansar, Malek Masoud Ansar, Safieh Danesh Mobarhan, Christian Agyare, Christian Agyare, Christian Agyare

PMC · DOI: 10.1371/journal.pone.0333647 · PLOS One · 2025-10-17

## TL;DR

Human fat cells show strong antibacterial effects against bacteria that resist a natural immune peptide, suggesting potential for treating tough infections.

## Contribution

Demonstrates hADSCs' antibacterial activity against LL-37-resistant pathogens, even when LL-37 levels drop after exposure.

## Key findings

- Conditioned media from hADSCs inhibited all three pathogens, with highest efficacy against Pseudomonas aeruginosa.
- LL-37 levels in conditioned media decreased after bacterial exposure, but antibacterial activity remained strong.
- hADSC secretomes show therapeutic potential for infections caused by LL-37-resistant bacteria.

## Abstract

Human adipose-derived stem cells (hADSCs) exhibit antibacterial properties, but their effectiveness against bacteria resistant to LL-37- a natural human antimicrobial peptide important in the immune defense- is not fully understood. Some bacteria have evolved mechanisms to evade the antimicrobial effects of LL-37. We aimed to investigate the antibacterial efficacy of hADSCs against Pseudomonas aeruginosa, Proteus mirabilis, and methicillin-resistant Staphylococcus aureus (MRSA), focusing on the antimicrobial peptide LL-37. hADSCs were isolated from human adipose tissue, identified by flow cytometry and differentiation assays, and divided into three groups: unstimulated, stimulated with interferon-gamma (IFN-γ; 100 ng/mL) or Escherichia coli (300 CFU). LL-37 gene expression was measured by qPCR after 6 hours in the E. coli stimulated group. LL-37 peptide levels were quantified by ELISA in conditioned media from unstimulated, IFN-γ stimulated cells, both before and after incubation with pathogens (300 CFU). Antibacterial activity was assessed by colony counting incubation following incubation of conditioned media with bacteria. Conditioned media from both unstimulated and stimulated hADSCs significantly inhibited growth of all three pathogens (P < 0.05), with highest efficacy against P. aeruginosa (86.4% inhibition), followed by MRSA (74%) and P. mirabilis (63%). LL-37 gene expression increased after bacterial stimulation, and also LL-37 concentrations increased in conditioned media but significantly decreased after bacterial exposure (P < 0.05). Despite this reduction, antibacterial activity persisted. hADSC-conditioned media exert potent antibacterial effects against LL-37-resistant pathogens, even when LL-37 levels are reduced after bacterial exposure. These findings support the therapeutic potential of hADSC secretomes, particularly for infections caused by bacteria capable of reducing LL-37 levels.

## Linked entities

- **Genes:** CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820]
- **Proteins:** CAMP (cathelicidin antimicrobial peptide)
- **Chemicals:** doxorubicin (PubChem CID 31703)
- **Species:** Pseudomonas aeruginosa (taxon 287), Proteus mirabilis (taxon 584), Staphylococcus aureus (taxon 1280), Escherichia coli (taxon 562), Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820] {aka CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26}
- **Diseases:** infections (MESH:D007239)
- **Chemicals:** methicillin (MESH:D008712)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280], Proteus mirabilis (species) [taxon 584], Escherichia coli (E. coli, species) [taxon 562], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12533887/full.md

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Source: https://tomesphere.com/paper/PMC12533887