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Published on: August 19, 2020
Plasma glycocalyx pattern: a mirror of endothelial damage in chronic kidney disease
Gemma Valera1, Andrea Figuer2,3, Jara Caro4
1Departamento de Genética, Fisiología y Microbiología, Facultad de Ciencias Biológicas, Universidad Complutense de Madrid/Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain.
Insights
Elevated perlecan in chronic kidney disease (CKD) correlates with pro-inflammatory monocytes. However, decorin may reduce monocyte inflammation, suggesting both are potential markers for endothelial damage in CKD patients.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Immunology
Background:
- Chronic kidney disease (CKD) is associated with endothelial damage and increased cardiovascular disease risk.
- Microinflammation and endothelial damage contribute to the heightened atherogenicity observed in CKD patients.
- Elevated levels of endothelial glycocalyx degradation products, including perlecan and decorin, are noted in CKD.
Purpose of the Study:
- To investigate the association between plasma perlecan and decorin levels and the pro-inflammatory and atherogenic state in CKD.
- To explore the relationship between these markers and monocyte subpopulations and intracellular adhesion molecule (ICAM)-1 expression in CKD patients.
Main Methods:
- Study included 17 healthy controls and 109 CKD patients (advanced CKD, hemodialysis, peritoneal dialysis, kidney transplantation).
- Plasma perlecan and decorin levels were quantified using enzyme-linked immunosorbent assays.
- Monocyte phenotype, including ICAM-1 expression, was analyzed via direct immunofluorescence and flow cytometry.
Main Results:
- Plasma perlecan levels were significantly higher in CKD patients compared to controls.
- Higher perlecan levels correlated with an increased prevalence of ICAM-1 positive monocytes.
- Advanced CKD patients exhibited higher decorin levels, associated with reduced ICAM-1 expression on monocytes.
Conclusions:
- Elevated perlecan in CKD may indicate a pro-inflammatory state linked to increased ICAM-1 positive monocytes.
- Elevated decorin might function as a negative regulator of ICAM-1 expression on monocytes.
- Perlecan and decorin show potential as biomarkers for inflammation, monocyte activation, and endothelial damage in CKD.
Background:
Endothelial damage and cardiovascular disease complicate chronic kidney disease (CKD). The increased atherogenicity observed in patients with CKD can be linked to microinflammation and endothelial damage. Circulating endothelial glycocalyx degradation products, such as perlecan and decorin, tend to be elevated in CKD. We aimed to explore the association between the plasma perlecan and decorin levels and this pro-inflammatory and atherogenic state by studying monocyte subpopulations and intracellular adhesion molecule (ICAM)-1 expression in patients with CKD.
Methods:
We studied 17 healthy controls, 23 patients with advanced CKD, 25 patients on haemodialysis, 23 patients on peritoneal dialysis and 20 patients who underwent kidney transplantation. Perlecan and decorin levels were evaluated using enzyme-linked immunosorbent assays, and the monocyte phenotype was analysed using direct immunofluorescence and flow cytometry.
Results:
The plasma perlecan levels were higher in patients with CKD than in the healthy controls. These levels were associated with a higher prevalence of ICAM-1+ monocytes. Conversely, patients with advanced CKD (pre-dialysis) had higher plasma decorin levels, which were associated with a reduced ICAM-1 expression per monocyte.
Conclusions:
Elevated perlecan levels in CKD may be associated with a higher prevalence of ICAM-1+ monocytes and a pro-inflammatory phenotype. Elevated decorin levels may act as a negative regulator of ICAM-1 expression in monocytes. Therefore, perlecan and decorin may be related to inflammation and monocyte activation in CKD and may act as potential markers of endothelial damage.
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