Literature DB >> 3534448

Nephronophthisis. A primary tubular basement membrane defect.

A H Cohen, J R Hoyer.   

Abstract

In order to characterize abnormalities in nephronophthisis, renal tissues from four patients were studied by light and electron microscopies and immunofluorescence using antibodies to laminin, type IV collagen, and tubular basement membranes (TBM). There were constant morphological alterations affecting TBM of all segments of the nephron, with or without cysts. These included extreme thinning and attenuation, layering, and thickening of these structures which ranged in size from 36 nm to 2000 nm. A combination of these features often affected the same TBM simultaneously, with abrupt transitions between different lesions. Although the ultrastructural TBM aberrations were observed in a wide variety of other chronic and acute renal disorders, they rarely occurred to the extent as in nephronophthisis or with abrupt transitions, both suggesting diagnostic significance. Laminin and type IV collagen were present in normal intensity and distribution, however, anti-TBM antibody staining was inconstantly reduced, perhaps signifying lack of a normal antigenic component in the TBM. These findings may well indicate the fundamental defect in nephronophthisis to be production of abnormal TBM, similar to the glomerular basement membrane lesions and consequences in Alport's syndrome.

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Year:  1986        PMID: 3534448

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  10 in total

1.  Senior-Loken syndrome. Case reports of two siblings and association with sensorineural deafness.

Authors:  M P Clarke; T J Sullivan; C Francis; R Baumal; T Fenton; W G Pearce
Journal:  Br J Ophthalmol       Date:  1992-03       Impact factor: 4.638

Review 2.  Comparative pathology of canine hereditary nephropathies: an interpretive review.

Authors:  C A Picut; R M Lewis
Journal:  Vet Res Commun       Date:  1987       Impact factor: 2.459

3.  Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.

Authors:  S Ala-Mello; E M Sankila; O Koskimies; A de la Chapelle; H Kääriäinen
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

4.  Role of extracellular matrix renal tubulo-interstitial nephritis antigen (TINag) in cell survival utilizing integrin (alpha)vbeta3/focal adhesion kinase (FAK)/phosphatidylinositol 3-kinase (PI3K)/protein kinase B-serine/threonine kinase (AKT) signaling pathway.

Authors:  Ping Xie; Vinay K Kondeti; Sun Lin; Yoshisuke Haruna; Kirtee Raparia; Yashpal S Kanwar
Journal:  J Biol Chem       Date:  2011-07-27       Impact factor: 5.157

5.  Poor renal uptake of 99mtechnetium-dimercaptosuccinic acid and near-normal 99mtechnetium-mercaptoacetyltriglycine renogram in nephronophthisis.

Authors:  H Hecht; J Ohlsson; S A Starck
Journal:  Pediatr Nephrol       Date:  1996-04       Impact factor: 3.714

6.  A tubulointerstitial nephritis antigen gene defect causes childhood-onset chronic renal failure.

Authors:  Yutaka Takemura; Machiko Koshimichi; Keisuke Sugimoto; Hidehiko Yanagida; Shinsuke Fujita; Tomoki Miyazawa; Kohei Miyazaki; Mitsuru Okada; Tsukasa Takemura
Journal:  Pediatr Nephrol       Date:  2010-02-16       Impact factor: 3.714

Review 7.  Imaging of fetal cystic kidney disease: multicystic dysplastic kidney versus renal cystic dysplasia.

Authors:  Mariana L Meyers; Amy L Treece; Brandon P Brown; Vijaya M Vemulakonda
Journal:  Pediatr Radiol       Date:  2020-11-30

8.  Infantile chronic tubulo-interstitial nephritis with cortical microcysts: variant of nephronophthisis or new disease entity?

Authors:  M F Gagnadoux; J L Bacri; M Broyer; R Habib
Journal:  Pediatr Nephrol       Date:  1989-01       Impact factor: 3.714

9.  Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study Group.

Authors:  F Hildebrandt; I Singh-Sawhney; B Schnieders; L Centofante; H Omran; A Pohlmann; C Schmaltz; H Wedekind; C Schubotz; C Antignac
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

Review 10.  The nephronophthisis complex: clinical and genetic aspects.

Authors:  F Hildebrandt; R Waldherr; R Kutt; M Brandis
Journal:  Clin Investig       Date:  1992-09
  10 in total

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