2. Academic Validation
  3. Endothelial CXCR2 deficiency attenuates renal inflammation and glycocalyx shedding through NF-κB signaling in diabetic kidney disease

Endothelial CXCR2 deficiency attenuates renal inflammation and glycocalyx shedding through NF-κB signaling in diabetic kidney disease

  • Cell Commun Signal. 2024 Mar 25;22(1):191. doi: 10.1186/s12964-024-01565-2.
Siyuan Cui # 1 2,  Xin Chen # 1 2 3,  Jiayu Li 4,  Wei Wang 4,  Deqi Meng 1 2 4,  Shenglong Zhu 5,  Shiwei Shen 6 7
Affiliations

Affiliations

  • 1 Department of Endocrinology, The Affiliated Wuxi No.2 People's Hospital of Nanjing Medical University, Wuxi, China.
  • 2 Department of Endocrinology, Jiangnan University Medical Center, Wuxi, China.
  • 3 Nanjing Medical University, Nanjing, China.
  • 4 Wuxi School of Medicine, Jiangnan University, Wuxi, China.
  • 5 Wuxi School of Medicine, Jiangnan University, Wuxi, China. [email protected].
  • 6 Department of Endocrinology, The Affiliated Wuxi No.2 People's Hospital of Nanjing Medical University, Wuxi, China. [email protected].
  • 7 Department of Endocrinology, Jiangnan University Medical Center, Wuxi, China. [email protected].
  • # Contributed equally.
PMID: 38528533 DOI: 10.1186/s12964-024-01565-2
Abstract

Background: The incidence of diabetic kidney disease (DKD) continues to rapidly increase, with limited available treatment options. One of the hallmarks of DKD is persistent inflammation, but the underlying molecular mechanisms of early diabetic kidney injury remain poorly understood. C-X-C Chemokine Receptor 2 (CXCR2), plays an important role in the progression of inflammation-related vascular diseases and may bridge between glomerular endothelium and persistent inflammation in DKD.

Methods: Multiple methods were employed to assess the expression levels of CXCR2 and its ligands, as well as renal inflammatory response and endothelial glycocalyx shedding in patients with DKD. The effects of CXCR2 on glycocalyx shedding, and persistent renal inflammation was examined in a type 2 diabetic mouse model with CXCR2 knockout specifically in endothelial cells (DKD-Cxcr2 eCKO mice), as well as in glomerular endothelial cells (GECs), cultured in high glucose conditions.

Results: CXCR2 was associated with early renal decline in DKD patients, and endothelial-specific knockout of CXCR2 significantly improved renal function in DKD mice, reduced inflammatory cell infiltration, and simultaneously decreased the expression of proinflammatory factors and chemokines in renal tissue. In DKD conditions, glycocalyx shedding was suppressed in endothelial CXCR2 knockout mice compared to CXCR2 L/L mice. Modulating CXCR2 expression also affected high glucose-induced inflammation and glycocalyx shedding in GECs. Mechanistically, CXCR2 deficiency inhibited the activation of NF-κB signaling, thereby regulating inflammation, restoring the endothelial glycocalyx, and alleviating DKD.

Conclusions: Taken together, under DKD conditions, activation of CXCR2 exacerbates inflammation through regulation of the NF-κB pathway, leading to endothelial glycocalyx shedding and deteriorating renal function. Endothelial CXCR2 deficiency has a protective role in inflammation and glycocalyx dysfunction, suggesting its potential as a promising therapeutic target for DKD treatment.

Keywords

CXCR2; Diabetic kidney disease; Glycocalyx shedding; Inflammation; NF-κB signaling.

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