Injury-Induced Epithelial Spp1 Engages Cd44 to Promote Neutrophil Recruitment and Exacerbate Acute Kidney Injury

This study provides the first evidence that tubular cell-derived Spp1 functions as a key DAMP mediating the early recruitment of Cd44<sup>+</sup> neutrophils in AKI. By inhibiting paracrine Spp1, 5-ASA limits neutrophil migration and ameliorates renal injury, supporting its therapeutic potential in AKI. Targeting Spp1 may represent a promising new strategy for AKI treatment.

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Publication Details

Journal
Journal of Inflammation Research
Published
2026-02-01
DOI
https://doi.org/10.2147/jir.s581725
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
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article

Injury-Induced Epithelial Spp1 Engages Cd44 to Promote Neutrophil Recruitment and Exacerbate Acute Kidney Injury

Zijian Zhang, Z H Zhao, Xiaopeng Hu, Runyi Wang et al.
Journal of Inflammation Research
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
article

Injury-Induced Epithelial Spp1 Engages Cd44 to Promote Neutrophil Recruitment and Exacerbate Acute Kidney Injury

Zijian Zhang, Z H Zhao, Xiaopeng Hu, Runyi Wang, Jiayu Wang, Xin Zheng
article en

Abstract

This study provides the first evidence that tubular cell-derived Spp1 functions as a key DAMP mediating the early recruitment of Cd44<sup>+</sup> neutrophils in AKI. By inhibiting paracrine Spp1, 5-ASA limits neutrophil migration and ameliorates renal injury, supporting its therapeutic potential in AKI. Targeting Spp1 may represent a promising new strategy for AKI treatment.

Journal of Inflammation ResearchVol. Volume 19
Capital Medical University (CN), Beijing Chao-Yang Hospital, Capital Medical University (CN), Capital Institute of Pediatrics (CN)
Openalex Percentile: Top 48%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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