# Non-polar components in PM2.5 increase matrix remodeling of CRS by up-regulating CEMIP in nasal fibroblasts

**Authors:** Jiayao Zhou, Ying Zhu, Huilin Hu, Ru Tang, Shiyao Zhang, Yuelong Gu, Song Mao, Shilei Pu, Hai Lin, Yue Zhao, Zhipeng Li, Weitian Zhang

PMC · DOI: 10.3389/fgene.2025.1672729 · Frontiers in Genetics · 2025-10-23

## TL;DR

Non-polar components in PM2.5, especially PAHs, worsen chronic rhinosinusitis by boosting nasal fibroblast migration and matrix remodeling.

## Contribution

Identifies non-polar organic components in PM2.5, particularly PAHs, as key drivers of CRS through CEMIP upregulation in nasal fibroblasts.

## Key findings

- Non-polar organic components (N-OC) significantly promote human nasal fibroblast migration.
- N-OC upregulates CEMIP, MMP1, and IL-1β expression in nasal fibroblasts.
- PAHs have a stronger effect on nasal fibroblasts compared to n-alkanes.

## Abstract

Fine particulate matter (PM2.5) is harmful to respiratory health and can lead to chronic rhinosinusitis (CRS). But how its components lead to CRS by affecting the function of nasal fibroblasts remains unclear.

In this study, polar organic components (P-OC) and non-polar organic components (N-OC) isolated from PM2.5 were used to intervene human nasal fibroblasts (hNFs), respectively. CCK8 assay and LDH assay were used to detect cell viability, and scratch assay was used to detect cell migration ability. Gene expression changes were detected by RNA-sequencing and molecular biology.

P-OC inhibited the viability and migration of hNFs, while N-OC significantly promoted the migration of hNFs. The expression of CEMIP, MMP1 and IL-1β was upregulated after N-OC treatment. CEMIP gene silencing inhibited hNFs migration and the expression of MMP1 and IL-1β. The effect of PAHs exposure on cells was more obvious than n-alkanes.

N-OC in PM2.5, especially PAHs, can aggravate CRS by activating hNFs through CEMIP. This study provides new ideas for exploring the pathogenic mechanism of air pollution on upper respiratory diseases.

## Linked entities

- **Genes:** CEMIP (cell migration inducing hyaluronidase 1) [NCBI Gene 57214], MMP1 (matrix metallopeptidase 1) [NCBI Gene 4312], IL1B (interleukin 1 beta) [NCBI Gene 3553]
- **Diseases:** chronic rhinosinusitis (MONDO:0006031), CRS (MONDO:0007399)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, MMP1 (matrix metallopeptidase 1) [NCBI Gene 4312] {aka CLG}, CEMIP (cell migration inducing hyaluronidase 1) [NCBI Gene 57214] {aka CCSP1, CEMIP1, HYBID, KIAA1199, TMEM2L}
- **Diseases:** CRS (MESH:D000092562), respiratory diseases (MESH:D012140)
- **Chemicals:** PAHs (MESH:D011084), n-alkanes (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12588579/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12588579/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12588579/full.md

---
Source: https://tomesphere.com/paper/PMC12588579