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足细胞病的病理学病变模式:方式与原因?

The Pathology Lesion Patterns of Podocytopathies: How and why?

作者信息

Ravaglia Fiammetta, Melica Maria Elena, Angelotti Maria Lucia, De Chiara Letizia, Romagnani Paola, Lasagni Laura

机构信息

Nephrology and Dialysis Unit, Santo Stefano Hospital, Prato, Italy.

Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Florence, Italy.

出版信息

Front Cell Dev Biol. 2022 Feb 24;10:838272. doi: 10.3389/fcell.2022.838272. eCollection 2022.

Abstract

Podocytopathies are a group of proteinuric glomerular disorders driven by primary podocyte injury that are associated with a set of lesion patterns observed on kidney biopsy, i.e., minimal changes, focal segmental glomerulosclerosis, diffuse mesangial sclerosis and collapsing glomerulopathy. These unspecific lesion patterns have long been considered as independent disease entities. By contrast, recent evidence from genetics and experimental studies demonstrated that they represent signs of repeated injury and repair attempts. These ongoing processes depend on the type, length, and severity of podocyte injury, as well as on the ability of parietal epithelial cells to drive repair. In this review, we discuss the main pathology patterns of podocytopathies with a focus on the cellular and molecular response of podocytes and parietal epithelial cells.

摘要

足细胞病是一组由原发性足细胞损伤驱动的蛋白尿性肾小球疾病,与肾活检中观察到的一系列病变模式相关,即微小病变、局灶节段性肾小球硬化、弥漫性系膜硬化和塌陷性肾小球病。长期以来,这些非特异性病变模式一直被视为独立的疾病实体。相比之下,最近来自遗传学和实验研究的证据表明,它们代表了反复损伤和修复尝试的迹象。这些持续的过程取决于足细胞损伤的类型、持续时间和严重程度,以及壁层上皮细胞驱动修复的能力。在这篇综述中,我们讨论了足细胞病的主要病理模式,重点是足细胞和壁层上皮细胞的细胞和分子反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7d/8907833/8dff8bee9b6c/fcell-10-838272-g001.jpg

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