Common histological patterns in glomerular epithelial cells in secondary focal segmental glomerulosclerosis

被引:60
|
作者
Kuppe, Christoph [1 ]
Groene, Hermann-Josef [2 ]
Ostendorf, Tammo [1 ]
van Kuppevelt, Toin H. [3 ]
Boor, Peter [4 ]
Floege, Juergen [1 ]
Smeets, Bart [1 ,5 ]
Moeller, Marcus J. [1 ]
机构
[1] RWTH Aachen Univ Hosp, Dept Internal Med Nephrol & Clin Immunol 2, Aachen, Germany
[2] German Canc Res Ctr, Dept Cellular & Mol Pathol, Heidelberg, Germany
[3] Radboud Univ Nijmegen, Med Ctr, Dept Biochem, NL-6525 ED Nijmegen, Netherlands
[4] RWTH Aachen Univ Hosp, Dept Pathol, Aachen, Germany
[5] Radboud Univ Nijmegen, Med Ctr, Dept Pathol, NL-6525 ED Nijmegen, Netherlands
关键词
chronic kidney disease; glomerulosclerosis; glomerulus; parietal epithelial cells; progression; renal biopsy; PODOCYTE; LESIONS; SCLEROSIS; DISEASES; DISTINCT; TUFT;
D O I
10.1038/ki.2015.116
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
Parietal epithelial cells (PECs) are involved in the development of sclerotic lesions in primary focal and segmental glomerulosclerosis (FSGS). Here, the role of PECs was explored in the more common secondary FSGS lesions in 68 patient biopsies, diagnosed with 11 different frequently or rarely encountered glomerular pathologies and additional secondary FSGS lesions. For each biopsy, one section was quadruple stained for PECs (ANXA3), podocytes (synaptopodin), PEC matrix (LKIV69), and Hoechst (nuclei), and a second was quadruple stained for activated PECs (CD44 and cytokeratin-19), PEC matrix, and nuclei. In all lesions, cellular adhesions (synechiae) between Bowman's capsule and the tuft were formed by cells expressing podocyte and/or PEC markers. Cells expressing PEC markers were detected in all FSGS lesions independent of the underlying glomerular disease and often stained positive for markers of activation. Small FSGS lesions, which were hardly identified on PAS sections previously, were detectable by immunofluorescent staining using PEC markers, potentially improving the diagnostic sensitivity to identify these lesions. Thus, similar patterns of cells expressing podocyte and/or PEC markers were found in the formation of secondary FSGS lesions independent of the underlying glomerular disease. Hence, our findings support the hypothesis that FSGS lesions follow a final cellular pathway to nephron loss that includes involvement of cells expressing PEC markers.
引用
收藏
页码:990 / 998
页数:9
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