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继发性局灶节段性肾小球硬化症肾小球上皮细胞的常见组织学模式。

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

机构信息

Department of Internal Medicine II, Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Aachen, Germany.

Department of Cellular and Molecular Pathology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Kidney Int. 2015 Nov;88(5):990-8. doi: 10.1038/ki.2015.116. Epub 2015 Apr 8.

Abstract

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.

摘要

壁细胞(PEC)参与原发性局灶节段性肾小球硬化症(FSGS)中硬化病变的发生。在这里,研究了 68 例患者活检中更常见的继发性 FSGS 病变中 PEC 的作用,这些患者被诊断为 11 种不同的常见或罕见肾小球病变以及其他继发性 FSGS 病变。对于每个活检,一个切片四重染色用于壁细胞(ANXA3)、足细胞(突触蛋白)、壁细胞基质(LKIV69)和 Hoechst(细胞核),第二个切片四重染色用于激活壁细胞(CD44 和角蛋白-19)、壁细胞基质和细胞核。在所有病变中,表达足细胞和/或 PEC 标志物的细胞在鲍曼囊和毛乳头之间形成细胞黏附(黏连)。在所有 FSGS 病变中都检测到表达 PEC 标志物的细胞,与潜在的肾小球疾病无关,并且经常对激活标志物呈阳性染色。以前在 PAS 切片上几乎无法识别的小 FSGS 病变,通过使用 PEC 标志物的免疫荧光染色可检测到,这可能提高了识别这些病变的诊断敏感性。因此,在不依赖于潜在肾小球疾病的情况下,在继发性 FSGS 病变的形成中发现了表达足细胞和/或 PEC 标志物的细胞的相似模式。因此,我们的发现支持 FSGS 病变遵循导致肾小球滤过单位丧失的最终细胞途径的假说,其中包括表达 PEC 标志物的细胞的参与。

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