Tubular CD146 expression in nephropathies is related to chronic renal failure

被引:19
作者
Daniel, L
Bardin, N
Moal, V
Dignat-George, F
Berland, Y
Figarella-Branger, D
机构
[1] Fac Med Marseille, IFR Physiopathol Humaine, FR-13385 Marseille, France
[2] INSERM, EMI 0019, Fac Pharm, F-13258 Marseille, France
[3] Concept Hosp, Dept Nephrol, Marseille, France
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2005年 / 99卷 / 04期
关键词
CD146; kidney; tubular cells; chronic renal failure; proteinuria;
D O I
10.1159/000083890
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: CD146, a member of the immunoglobulin superfamily, is mainly expressed at the endothelial junction. The soluble form of CD146 is increased in the serum of patients with chronic renal failure. The aim of the study was to investigate CD146 expression on biopsies of normal kidney and nephropathies. Methods: We did an immunohistochemical analysis of 10 normal renal tissues and 126 patients with nephropathies. Results: The mean age of the patients was 47.5 +/- 18 years with 65% of men. At the time of the biopsy, 73 patients (57.9%) had a renal failure and the mean proteinuria was 3.3 +/- 2.9 g/ 24 h. Inflammatory syndrome was present in 60 (47.6%) patients. Fibrous interstitial changes from minimal lesions to diffuse lesions were seen in 105 (83.3%) biopsies; the mean glomerulosclerosis index was 16.9 +/- 19.7%. Normal kidneys showed CD146 staining on endothelial cells, smooth muscle cells, and mesangium. Normal tubular cells were not stained. If endocapillary proliferation was present, the mesangial CD146 expression was higher. This mesangial expression correlated with proteinuria ( p = 0.007) and not with renal failure ( p = 0.07). A de novo expression on tubular cells was found in 53 patients (42%) and this expression correlated with age ( p < 0.001), male sex ( p = 0.04), glomerulosclerosis ( p < 0.001), interstitial fibrosis ( p < 0.001), and renal failure ( p < 0.001). Conclusion: Renal CD146 expression is of interest for determining the pathogenesis of mesangial alterations during glomerular injuries and of tubular phenotypic changes during chronic renal failure. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:E105 / E111
页数:7
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