# Staphylococcus aureus utilizes vimentin to internalize human keratinocytes

**Authors:** Kyoungok Jang, Hangeun Kim, Dobin Choi, Soojin Jang, Dae-Kyun Chung

PMC · DOI: 10.3389/fcimb.2025.1543186 · Frontiers in Cellular and Infection Microbiology · 2025-02-21

## TL;DR

Staphylococcus aureus uses the protein vimentin to infect human skin cells, and this process involves specific signaling pathways.

## Contribution

This study reveals that S. aureus induces vimentin expression and uses it to enhance infection in human keratinocytes.

## Key findings

- Live S. aureus increases vimentin expression in HaCaT cells through TLR2 signaling.
- Vimentin secreted by infected cells binds to S. aureus and promotes intracellular infection.
- Heat-killed bacteria and supernatants do not induce vimentin expression.

## Abstract

Vimentin is an intermediate filamentous cytoskeletal protein involved in cell migration, adhesion, and division. Recent studies have demonstrated that several bacteria and viruses interact with vimentin to facilitate entry and trafficking within eukaryotic cells. However, the relationship between Staphylococcus aureus and vimentin remains unclear.

In the current study, we elucidated vimentin expression mechanism in human keratinocytes infected with S. aureus using Western blot (WB), Flow cytometry, Immunofluorescence (IF) staining, utilizing neutralizing antibodies, and small interference (si) RNA, and a vimentin overexpression vector. The physical interaction between vimentin and S. aureus was shown by IF on cell surface, intra- and intercellular space.

HaCaT cells increased vimentin expression through physical interaction with live S. aureus, and not by heat-killed bacteria or bacterial culture supernatants. The Toll-like receptor (TLR) 2 signaling pathway, which includes interleukin 1 receptor-associated kinase (IRAK) and nuclear factor kappa B (NF-κB)/c-Jun N-terminal kinase (JNK) signaling activation, was involved in S. aureus-mediated vimentin expression. The vimentin protein induced by S. aureus was secreted extracellularly and bound to S. aureus in the culture media. The binding of vimentin to S. aureus accelerated the intracellular infection of HaCaT cells.

Thus, these experiments elucidated the mechanism of vimentin protein expression during S. aureus infection in human skin keratinocytes and revealed the role of vimentin in this process. These findings suggest that vimentin could serve as a potential target for the prevention or treatment of S. aureus infections.

## Linked entities

- **Genes:** TLR2 (toll like receptor 2) [NCBI Gene 7097], IRAK1 (interleukin 1 receptor associated kinase 1) [NCBI Gene 3654], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], MAPK8 (mitogen-activated protein kinase 8) [NCBI Gene 5599]
- **Proteins:** PRELID1 (PRELI domain containing 1)
- **Species:** Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Diseases:** infection (MESH:D007239)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280]
- **Cell lines:** HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11885264/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC11885264/full.md

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Source: https://tomesphere.com/paper/PMC11885264