Literature DB >> 25845564

Heymann nephritis in Lewis rats.

Yuan Min Wang1, Vincent W S Lee2, Huiling Wu3, David C H Harris2, Stephen I Alexander1.   

Abstract

Human membranous nephritis is a major cause of end-stage kidney disease. Active Heymann nephritis (HN) is an auto-immune model of membranous nephritis induced in Lewis rats by immunization with a crude renal tubular antigen (Fx1A) or megalin (gp330). The pathogenesis of HN is through the binding of anti-Fx1A autoantibodies to the auto-antigen expressed on glomerular epithelial cells, resulting in severe glomerular injury and proteinuria. The pathological features of HN include immune deposits in glomeruli and infiltration of glomeruli and the tubulointerstitium by macrophages and T cells. This unit describes the method of the preparation of Fx1A and the induction of HN in Lewis rats by immunization with Fx1A.
Copyright © 2015 John Wiley & Sons, Inc.

Entities:  

Keywords:  Fx1A; Lewis rats; active Heymann nephritis; glomerulonephritis; proteinuria

Mesh:

Substances:

Year:  2015        PMID: 25845564     DOI: 10.1002/0471142735.im1529s109

Source DB:  PubMed          Journal:  Curr Protoc Immunol        ISSN: 1934-3671


  2 in total

1.  VEGFA promotes the occurrence of PLA2R-associated idiopathic membranous nephropathy by angiogenesis via the PI3K/AKT signalling pathway.

Authors:  Ben Ke; Jinjing Huang; Zhibing Duan; Wen Shen; Yao Wu; Weiping Tu; Xiangdong Fang
Journal:  BMC Nephrol       Date:  2022-09-16       Impact factor: 2.585

Review 2.  B Cells in Primary Membranous Nephropathy: Escape from Immune Tolerance and Implications for Patient Management.

Authors:  Benjamin Y F So; Desmond Y H Yap; Tak Mao Chan
Journal:  Int J Mol Sci       Date:  2021-12-17       Impact factor: 5.923

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.