# Skin Barrier-Improving and Anti-Inflammatory Effects of Exosomes Derived from the Fructobacillus fructosus NSH-1 Strain Isolated from the Campsis grandiflora Flower

**Authors:** Byeong-Min Choi, Hyehyun Hong, Yeon-Bo Jang, Tae-Jin Park, Seung-Young Kim

PMC · DOI: 10.4014/jmb.2512.12008 · Journal of Microbiology and Biotechnology · 2026-03-12

## TL;DR

Exosomes from a bacteria found in Campsis grandiflora flowers show anti-inflammatory and skin barrier-improving effects in cell studies.

## Contribution

The study identifies exosomes from Fructobacillus fructosus NSH-1 as novel bioactive agents for skin health.

## Key findings

- NSH-1 exosomes inhibit pro-inflammatory mediators like TNF-α, IL-6, and PGE2 in a concentration-dependent manner.
- Treatment with NSH-1 exosomes enhances skin barrier function by increasing hyaluronan, collagen, and wound healing.
- Exosomes reduce iNOS and COX-2 expression while upregulating filaggrin, involucrin, and loricrin proteins.

## Abstract

This study investigated the anti-inflammatory and skin barrier-improving activities of Fructobacillus fructosus strain NSH-1-derived exosomes in LPS-stimulated RAW 264.7 cells and HaCaT cells. Nanoparticle tracking and transmission electron microscopy analyses confirmed the concentration, purity, and morphology of NSH-1 exosomes. The exosomes showed no cytotoxicity at concentrations of 1.5 × 107, 3.0 × 107, and 6.0 × 107 particles/ml, but demonstrated concentration-dependent inhibitory activity against nitric oxide production. Furthermore, NSH-1 exosomes significantly inhibited the production of pro-inflammatory mediators, including TNF-α, IL-6, IL-1β, and PGE2. In HaCaT cells, treatment with NSH-1 exosomes enhanced skin barrier function by increasing the production of hyaluronan and collagen in a concentration-dependent manner and promoting wound-healing activity. Western blot analysis revealed that treatment with NSH-1 exosomes reduced the expression levels of inflammatory proteins iNOS and COX-2, while increasing the expression of skin barrier-related proteins such as filaggrin, involucrin, and loricrin. Overall, these findings indicate that NSH-1 exosomes exert strong anti-inflammatory activity by suppressing the expression of the pro-inflammatory cytokines iNOS and COX-2, while simultaneously enhancing skin barrier integrity by upregulating filaggrin, involucrin, and loricrin. Thus, exosomes derived from F. fructosus NSH-1, isolated from Campsis grandiflora flowers, demonstrate promise as natural bioactive agents for anti-inflammatory and skin barrier-improving applications.

## Linked entities

- **Proteins:** NOS2 (nitric oxide synthase 2), COX2 (cytochrome c oxidase subunit II), LOC102285057 (hornerin), LOC102087249 (keratin-associated protein 10-9), LORICRIN (loricrin cornified envelope precursor protein), TNF (tumor necrosis factor), IL6 (interleukin 6), IL1B (interleukin 1 beta), ptges2.L (prostaglandin E synthase 2 L homeolog)
- **Species:** Fructobacillus fructosus (taxon 1631), Campsis grandiflora (taxon 108594)

## Full-text entities

- **Genes:** LORICRIN (loricrin cornified envelope precursor protein) [NCBI Gene 4014] {aka LOR}, ISYNA1 (inositol-3-phosphate synthase 1) [NCBI Gene 51477] {aka INO1, INOS, IPS, IPS 1, IPS-1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, FLG (filaggrin) [NCBI Gene 2312] {aka ATOD2, FLG-1, FLG1}, IVL (involucrin) [NCBI Gene 3713], COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** cytotoxicity (MESH:D064420), Inflammatory (MESH:D007249)
- **Chemicals:** NSH-1 (-), LPS (MESH:D008070), hyaluronan (MESH:D006820), nitric oxide (MESH:D009569)
- **Species:** Fructobacillus fructosus (species) [taxon 1631], Campsis grandiflora (Chinese trumpet-creeper, species) [taxon 108594]

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12991936/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12991936/full.md

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Source: https://tomesphere.com/paper/PMC12991936