Literature DB >> 7604502

Early ultrastructural glomerular alterations in neonatal nephrotic mice (ICGN strain).

A Ogura1, H Fujimura, T Asano, M Koura, I Naito, Y Kobayashi.   

Abstract

ICGN is a strain of mice with hereditary nephrotic syndrome of an unknown cause. In this study, early glomerular alterations in newborn ICGN mice were observed with electron microscopy to gain a better insight into the onset of the disease. Development of the glomeruli was normal until fusion of epithelial and endothelial basement membranes in the developing capillary stage. From the maturing glomerulus stage onward, the fused glomerular basement membrane (GBM) increased in thickness by excessive accumulation of the basement membrane material secreted from the epithelial cells. This accumulation was followed by overall loss of epithelial foot processes in the glomeruli. These findings indicate that the disease in ICGN mice is caused by some defect(s) in the GMB maturation process, which may be crucial for the generation of the glomerular permselectivity.

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Year:  1995        PMID: 7604502     DOI: 10.1177/030098589503200317

Source DB:  PubMed          Journal:  Vet Pathol        ISSN: 0300-9858            Impact factor:   2.221


  10 in total

1.  Deficiency of the tensin2 gene in the ICGN mouse: an animal model for congenital nephrotic syndrome.

Authors:  A-Ri Cho; Kozue Uchio-Yamada; Takeshi Torigai; Tomomi Miyamoto; Ichiro Miyoshi; Junichiro Matsuda; Tsutomu Kurosawa; Yasuhiro Kon; Atsushi Asano; Nobuya Sasaki; Takashi Agui
Journal:  Mamm Genome       Date:  2006-05       Impact factor: 2.957

2.  Transforming growth factor-beta1 mediated up-regulation of lysyl oxidase in the kidneys of hereditary nephrotic mouse with chronic renal fibrosis.

Authors:  Yasufumi Goto; Kozue Uchio-Yamada; Sayuri Anan; Yoshie Yamamoto; Atsuo Ogura; Noboru Manabe
Journal:  Virchows Arch       Date:  2005-08-05       Impact factor: 4.064

3.  A Decrease in Glomerular Endothelial Cells and Endothelial-mesenchymal Transition during Glomerulosclerosis in the Tensin2-deficient Mice (ICGN strain).

Authors:  Takashi Kato; Shinya Mizuno; Akihiko Ito
Journal:  Acta Histochem Cytochem       Date:  2014-11-21       Impact factor: 1.938

4.  Mouse chromosome 2 harbors genetic determinants of resistance to podocyte injury and renal tubulointerstitial fibrosis.

Authors:  Hayato Sasaki; Junpei Kimura; Ken-Ichi Nagasaki; Kiyoma Marusugi; Takashi Agui; Nobuya Sasaki
Journal:  BMC Genet       Date:  2016-05-26       Impact factor: 2.797

5.  Nephron, Wilms' tumor-1 (WT1), and synaptopodin expression in developing podocytes of mice.

Authors:  Takashi Kato; Shinya Mizuno
Journal:  Exp Anim       Date:  2017-02-07

Review 6.  Tensin 2-deficient nephropathy: mechanosensitive nephropathy, genetic susceptibility.

Authors:  Hayato Sasaki; Nobuya Sasaki
Journal:  Exp Anim       Date:  2022-04-19

7.  Analysis of ultrastructural glomerular basement membrane lesions and podocytes associated with proteinuria and sclerosis in Osborne-Mendel rats with progressive glomerulonephropathy.

Authors:  Kyohei Yasuno; Junichi Kamiie; Kinji Shirota
Journal:  J Vet Sci       Date:  2013-06-21       Impact factor: 1.672

8.  Quantitative trait Loci for resistance to the congenital nephropathy in tensin 2-deficient mice.

Authors:  Hayato Sasaki; Nobuya Sasaki; Tomohiro Nishino; Ken-Ichi Nagasaki; Hiroshi Kitamura; Daisuke Torigoe; Takashi Agui
Journal:  PLoS One       Date:  2014-06-26       Impact factor: 3.240

9.  Spontaneous early-onset glomerulonephritis in a 8-week-old male Crj:CD1 (ICR) mouse.

Authors:  Kyohei Ago; Go Sugahara; Kinji Shirota; Yasushi Kurata
Journal:  J Toxicol Pathol       Date:  2015-09-04       Impact factor: 1.628

10.  Genetic loci for resistance to podocyte injury caused by the tensin2 gene deficiency in mice.

Authors:  Yuki Takahashi; Hayato Sasaki; Shiori Okawara; Nobuya Sasaki
Journal:  BMC Genet       Date:  2018-04-10       Impact factor: 2.797

  10 in total

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