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Significance of CD163-Positive Macrophages in Proliferative Glomerulonephritis
Jun Li1, Chang-Hua Liu, Dao-Liang Xu
1Department of Nephrology, Clinical Medical College, Yangzhou University, Yangzhou, China.
Background:
CD163, a marker of M2 macrophages, possesses anti-inflammatory properties. This study aims to investigate the clinicopathological significance of CD163-positive macrophages in proliferative glomerulonephritis.
Methods:
Renal tissue samples from patients with lupus nephritis (LN, n = 22), antineutrophil cytoplasmic autoantibody (ANCA)-associated pauci-immune necrotizing glomerulonephritis (PNGN, n = 10), type 1 membranoproliferative glomerulonephritis (n = 5), minimal change disease (n = 8) and normal control kidneys (n = 3) were included in this study. The expression of CD163, CD68, CD20 and CD3 in renal tissues was detected by immunohistochemistry or immunofluorescence. The level of urinary neutrophil gelatinase-associated lipocalin (NGAL) was determined by enzyme-linked immunosorbent assay.
Results:
CD163 was mainly expressed in active crescentic glomerulonephritis, proliferative glomerular lesions and areas of tubulointerstitial injury. Patients with LN-IV and PNGN had numerous CD163-positive cells in glomerular and acute tubulointerstitial lesions. CD163-positive cells in glomeruli positively correlated to proteinuria yet negatively correlated to estimated glomerular filtration rate. There was a positive correlation between the number of CD163 cells in acute tubulointerstitial lesions and NGAL levels, whereas a negative correlation between CD163 numbers and estimated glomerular filtration rate. The number of CD163-positive cells in crescentic glomerulonephritis was more than other groups. In LN, the number of CD163 cells in the tubulointerstitial and glomerular lesions had a positive correlation with activity index. Dual staining showed that CD163-positive cells also expressed CD68, although they did not show any staining for CD20 or CD3.
Conclusions:
CD163-positive macrophages were involved in the pathogenesis of proliferative glomerular lesions, active crescentic glomerulonephritis and acute tubular injury of patients with PNGN and active LN.
Insights
CD163-positive macrophages are linked to kidney damage in proliferative glomerulonephritis and lupus nephritis. Their presence correlates with disease severity and impaired kidney function, suggesting a role in disease progression.
Area of Science:
- Nephrology
- Immunology
- Pathology
Background:
- CD163 is an M2 macrophage marker with anti-inflammatory properties.
- The role of CD163-positive macrophages in proliferative glomerulonephritis is not fully understood.
Purpose of the Study:
- To investigate the clinicopathological significance of CD163-positive macrophages in proliferative glomerulonephritis.
- To explore the association of CD163 expression with disease activity and renal function.
Main Methods:
- Renal tissue samples from patients with lupus nephritis (LN), ANCA-associated pauci-immune necrotizing glomerulonephritis (PNGN), and other kidney diseases were analyzed.
- Immunohistochemistry/immunofluorescence was used to detect CD163, CD68, CD20, and CD3 expression.
- Urinary neutrophil gelatinase-associated lipocalin (NGAL) levels were measured.
Main Results:
- CD163 was highly expressed in active crescentic glomerulonephritis, proliferative glomerular lesions, and tubulointerstitial injury, particularly in LN and PNGN.
- Glomerular CD163 correlated positively with proteinuria and negatively with estimated glomerular filtration rate (eGFR).
- Tubulointerstitial CD163 correlated positively with urinary NGAL and negatively with eGFR, and was associated with higher activity index in LN.
Conclusions:
- CD163-positive macrophages are implicated in the pathogenesis of proliferative glomerulonephritis, crescentic glomerulonephritis, and acute tubular injury.
- These macrophages play a role in active lupus nephritis and ANCA-associated pauci-immune necrotizing glomerulonephritis.
- CD163 expression serves as a potential biomarker for disease severity and progression in these conditions.
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