Literature DB >> 9435688

Slit diaphragm-reactive nephritogenic MAb 5-1-6 alters expression of ZO-1 in rat podocytes.

H Kawachi1, H Kurihara, P S Topham, D Brown, M A Shia, M Orikasa, F Shimizu, D J Salant.   

Abstract

Monoclonal antibody (MAb) 5-1-6 identifies a 51-kDa protein (p51) on rat podocyte foot processes and causes severe complement- and leukocyte-independent proteinuria when injected into rats. In the studies reported here, we used various immunohistological techniques to define the precise location of p51 and its relationship to ZO-1, a known component of the podocyte slit diaphragm in adult rat glomeruli. Our results demonstrate that p51 and ZO-1 lie close to each other on opposite sides of the podocyte plasma membrane at the point of insertion of the slit diaphragm: ZO-1 on the cytoplasmic face and p51 on the slit diaphragm and adjoining outer leaflet of the plasma membrane bordering the filtration slits. In addition to their geographic proximity, there appears to be a relationship between p51 and ZO-1. After MAb 5-1-6 injection, there was a progressive decline in stainable ZO-1 in the podocytes of heavily proteinuric rats. In addition, Western blot analysis of glomerular lysates showed that the decline in staining was due to a loss of immunoreactive ZO-1 rather than redistribution or diffusion of the protein. Simultaneously, the distribution of glomerular-bound MAb 5-1-6 became more clumped, apparently because of partial endocytosis into a lysosomal compartment, while the slit diaphragms remained morphologically intact. These findings suggest that MAb 5-1-6 alters the molecular composition of the slit diaphragm and thereby affects the glomerular permeability barrier.

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Year:  1997        PMID: 9435688     DOI: 10.1152/ajprenal.1997.273.6.F984

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  17 in total

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4.  Nephritogenic mAb 5-1-6 is directed at the extracellular domain of rat nephrin.

Authors:  P S Topham; H Kawachi; S A Haydar; S Chugh; T A Addona; K B Charron; L B Holzman; M Shia; F Shimizu; D J Salant
Journal:  J Clin Invest       Date:  1999-12       Impact factor: 14.808

5.  Angiotensin II type 1 receptor blockade ameliorates proteinuria in puromycin aminonucleoside nephropathy by inhibiting the reduction of NEPH1 and nephrin.

Authors:  Aya Takahashi; Yoshiyasu Fukusumi; Mihoko Yamazaki; Mutsumi Kayaba; Yukina Kitazawa; Masayuki Tomita; Hiroshi Kawachi
Journal:  J Nephrol       Date:  2014-10-09       Impact factor: 3.902

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7.  High-glucose and advanced glycosylation end products increased podocyte permeability via PI3-K/Akt signaling.

Authors:  Tae-Sun Ha
Journal:  J Mol Med (Berl)       Date:  2010-01-08       Impact factor: 4.599

Review 8.  Slit diaphragm dysfunction in proteinuric states: identification of novel therapeutic targets for nephrotic syndrome.

Authors:  Hiroshi Kawachi; Koichi Suzuki; Naoko Miyauchi; Taeko Hashimoto; Yasuhiro Otaki; Fujio Shimizu
Journal:  Clin Exp Nephrol       Date:  2009-03-07       Impact factor: 2.801

Review 9.  Idiopathic nephrotic syndrome: the EBV hypothesis.

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Journal:  Pediatr Res       Date:  2016-09-28       Impact factor: 3.756

10.  Impact of cyclosporin on podocyte ZO-1 expression in puromycin aminonucleoside nephrosis rats.

Authors:  Beom Seok Kim; Hyeong Cheon Park; Shin Wook Kang; Kyu Hun Choi; Sung Kyu Ha; Dae Suk Han; Ho Yung Lee
Journal:  Yonsei Med J       Date:  2005-02-28       Impact factor: 2.759

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