# Impact of Particulate Matter on the Exacerbation of Immunoglobulin A Nephropathy: An Animal Experimental Study

**Authors:** Minhyeok Lee, Yeon Woo Lee, Daeun Kang, Ji Woong Son, Wan Jin Hwang, Sin Yung Woo, Mi Jin Hong, Yusin Pak, Se-Hee Yoon, Won Min Hwang, Sung-Ro Yun, Yohan Park

PMC · DOI: 10.3390/ijms26199387 · 2025-09-25

## TL;DR

This study shows that exposure to particulate matter worsens immunoglobulin A nephropathy in mice through immune system activation.

## Contribution

The study experimentally demonstrates that PM exposure exacerbates IgAN via TLR9-mediated immune activation and aberrant IgA glycosylation.

## Key findings

- PM exposure increased lung TLR9 expression and was associated with pigment-laden macrophages.
- HIGA mice exposed to PM showed elevated aberrant IgA and APRIL levels with worsened kidney pathology.
- Transcriptomic analysis revealed immune dysregulation in splenic B cells of PM-exposed HIGA mice.

## Abstract

Particulate matter (PM) exposure is linked to chronic kidney disease; however, its effect on immunoglobulin A (IgA) nephropathy (IgAN) remains unclear. We investigated whether PM exposure exacerbates IgAN in a mouse model. HIGA mice (IgAN model) and BALB/c controls were exposed to PM in a sealed chamber for 13 weeks. Lung Toll-like receptor 9 (TLR9) expression, serum aberrantly glycosylated IgA, A proliferation-inducing ligand (APRIL) levels, mesangial IgA deposition, and kidney pathology were assessed. RNA sequencing of splenic B cells was performed to evaluate immune-related gene expression. PM exposure increased lung TLR9 expression in both strains, particularly around pigment-laden macrophages. HIGA mice showed elevated aberrant IgA and APRIL levels, with aggravated mesangial expansion and IgA deposition. Transcriptomic analysis revealed immune dysregulation in splenic B cells of PM-exposed HIGA mice. Our findings provide experimental evidence that PM exposure aggravates IgAN via TLR9-mediated mucosal immune activation, leading to aberrant IgA glycosylation and mesangial deposition. These findings emphasize that reducing PM exposure may benefit patients with IgAN.

## Linked entities

- **Genes:** TLR9 (toll like receptor 9) [NCBI Gene 54106]
- **Proteins:** CD79A (CD79a molecule), TNFSF13 (TNF superfamily member 13)
- **Diseases:** chronic kidney disease (MONDO:0005300)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Tnfsf13 (tumor necrosis factor (ligand) superfamily, member 13) [NCBI Gene 69583] {aka 2310026N09Rik, April, Tall2, Tnlg7b, Trdl1}, Tlr9 (toll-like receptor 9) [NCBI Gene 81897]
- **Diseases:** chronic kidney disease (MESH:D051436), Immunoglobulin A Nephropathy (MESH:D005922)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12525145/full.md

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Source: https://tomesphere.com/paper/PMC12525145