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Podocytes undergo phenotypic changes and express macrophagic-associated markers in idiopathic collapsing glomerulopathy

机译:足细胞经历表型改变并在特发性萎缩性肾小球病中表达巨噬细胞相关标记

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Podocytes undergo phenotypic changes and express macrophagic-associated markers in idiopathic collapsing glomerulopathy. Collapsing glomerulopathy (CG), a severe form of focal segmental glomerulosclerosis (FSG), is characterized by tuft retraction and consolidation in numerous glomeruli and changes in podocyte morphology and topography. Other glomeruli are less affected. Collapsing glomerulopathy is also characterized by tubulointerstitial atrophy and fibrosis. The pathophysiology of the glomerular and tubulointerstitial lesions is poorly understood. We studied renal tissue of five Black and three White patients, all human immunodeficiency virus (HIV) negative, with nephrotic syndrome, renal failure, and histological evidence of CG. Immunohistochemistry identified normal podocyte phenotypes by podocalyxin, vimentin and complement receptor 1 (CR1) labeling. Three monoclonal antibodies were used to further characterize podocyte epitopes: anti-CD68 clone KP1, anti-CD68 clone PG-M1 and anti-M130 clone M18 (Ber-MAC3). Light microscopy of collapsed glomeruli showed podocyte swelling, vacuolization, multinucleation, "cobblestone-like" alignment around the glomerular tuft, and pseudo-crescent formation in Bowman's space. In collapsed glomeruli, podocalyxin, vimentin and CR1 labeling tagged both normal and vacuolated podocytes still attached to the GBM, but labeling was not found in cobblestone-like podocytes or in podocytes detached from the GBM. Conversely, numerous podocytes undergoing detachment and shedding into Bowman's space expressed macrophagic-associated epitopes. Cells with macrophagic-associated epitopes clumped in cystically dilated tubules and were aligned in tubules of smaller caliber. Their appearance was that of viable cells. There was no morphologic indication that these cells expressing macrophage-associated antigens originated from outside the glomeruli or outside the tubules. We conclude that in CG podocytes detach from the GBM, lose their normal podocytic phenotype and acquire macrophage differentiation antigens. The presence of cells with such antigens in tubular lumens suggests that detached metaplastic podocytes progress along the tubule or, alternatively, that CG tubular cells also undergo metaplastic changes into macrophage-like cells.
机译:足细胞发生表型变化,并在特发性萎缩性肾小球病中表达巨噬细胞相关标记。塌陷性肾小球病(CG)是局灶性节段性肾小球硬化(FSG)的一种严重形式,其特征是簇簇在许多肾小球内缩回和合并,以及足细胞形态和地形的变化。其他肾小球受影响较小。肾小球塌陷的特征还在于肾小管间质萎缩和纤维化。肾小球和肾小管间质病变的病理生理了解甚少。我们研究了五名黑人和三名白人患者的肾脏组织,所有人类免疫缺陷病毒(HIV)阴性,具有肾病综合征,肾衰竭和CG的组织学证据。免疫组织化学通过podocalyxin,波形蛋白和补体受体1(CR1)标记鉴定出正常的足细胞表型。使用三种单克隆抗体进一步表征足细胞表位:抗CD68克隆KP1,抗CD68克隆PG-M1和抗M130克隆M18(Ber-MAC3)。塌陷的肾小球的光学显微镜显示足细胞肿胀,空泡化,多核化,肾小球簇周围的“鹅卵石状”排列以及鲍曼空间中的假新月形形成。在塌陷的肾小球中,足突霉素,波形蛋白和CR1标记标记仍附着在GBM上的正常足泡和空泡足细胞,但在鹅卵石样足细胞或从GBM分离的足细胞中未发现标记。相反,大量脱离和脱落进入鲍曼氏空间的足细胞表达了巨噬细胞相关表位。具有巨噬细胞相关表位的细胞在囊状扩张的小管中聚集,并在较小口径的小管中排列。它们的外观是活细胞的外观。没有形态学迹象表明这些表达巨噬细胞相关抗原的细胞起源于肾小球外或肾小管外。我们得出的结论是,CG足细胞脱离了GBM,失去了正常的足细胞表型,并获得了巨噬细胞分化抗原。肾小管腔中含有这种抗原的细胞的存在表明,脱离的化生足细胞沿着小管前进,或者,CG肾小管细胞也经历了化生改变,变成了巨噬细胞样细胞。

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