CXCL5 inhibition improves kidney function by protecting renal tubular epithelial cells in diabetic kidney disease.
Journal
Clinical immunology
Journal Volume
268
ISSN
1521-7035
Date Issued
2024-11
Author(s)
DOI
10.1016/j.clim.2024.110369
Abstract
Inflammation is one of exacerbating factors of diabetic kidney disease (DKD). Upregulated CXCL5 is found in clinical and experimental diabetes studies. This study aimed to investigate the impact and mechanism of CXCL5 on DKD. DKD patients with different levels of urine albumin-to-creatinine ratio were enrolled. Lepr mice and CXCL5-knockout diabetic mice were used as mouse models for DKD. Human renal tubular epithelial cells were used for in vitro experiments. Circulating CXCL5 were increased in DKD patients compared to the non-DKD subjects. CXCL5 inhibition through CXCL5-neutralizing antibodies or genetic knockout improved kidney function and ameliorated tubular injury and renal fibrosis. In high-glucose-stimulated tubular epithelial cells, administration of CXCL5-neutralizing antibodies or siRNA resulted in reduced phospho-JNK/c-JUN/p65 and the downstream inflammatory, fibrotic, and apoptotic protein expressions. Administration of CXCR2 and JNK inhibitors impeded the CXCL5-induced tubular epithelial cell damages. In conclusion, these findings indicated that anti-CXCL5 strategies may be potential treatments for DKD.
Subjects
Chemokine CXC motif ligand 5
Diabetic kidney disease
Fibrosis
Inflammation
Renal tubular epithelial cell
SDGs
Publisher
Academic Press Inc.
Description
Article Number : 110369
Type
journal article