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特发性膜性肾病的实验模型研究进展(综述)。

Advances of the experimental models of idiopathic membranous nephropathy (Review).

机构信息

Key Laboratory of Chinese Internal Medicine of The Ministry of Education and Beijing, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine, Beijing 100700, P.R. China.

Beijing Chinese Medicine Hospital Pinggu Hospital, Beijing 101200, P.R. China.

出版信息

Mol Med Rep. 2020 May;21(5):1993-2005. doi: 10.3892/mmr.2020.11014. Epub 2020 Mar 9.

Abstract

Idiopathic membranous nephropathy (IMN) is one of the main types of chronic kidney disease in adults and one of the most common causes of end‑stage renal disease. In recent years, the morbidity of IMN among primary glomerular diseases has markedly increased, while the pathogenesis of the disease remains unclear. To address this, a number of experimental models, including Heymann nephritis, anti‑thrombospondin type‑1 domain‑containing 7A antibody‑induced IMN, cationic bovine serum albumin, anti‑human podocyte antibodies and zymosan‑activated serum‑induced C5b‑9, have been established. This review comprehensively summarized the available animal and cell models for IMN. The limitations and advantages of the current models were discussed and two improved models were introduced to facilitate the selection of an appropriate model for further studies on IMN.

摘要

特发性膜性肾病(IMN)是成人慢性肾脏病的主要类型之一,也是终末期肾病的最常见病因之一。近年来,原发性肾小球疾病中 IMN 的发病率显著增加,但其发病机制尚不清楚。为此,建立了多种实验模型,包括马兜铃酸肾病、抗血栓素型 1 结构域包含 7A 抗体诱导的 IMN、阳离子牛血清白蛋白、抗人足细胞抗体和酵母聚糖激活血清诱导的 C5b-9。本综述全面总结了现有的 IMN 动物和细胞模型。讨论了当前模型的局限性和优势,并介绍了两种改进的模型,以方便选择合适的模型,进一步研究 IMN。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8faa/7115214/1400f78dc7ea/MMR-21-05-1993-g00.jpg

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