Literature DB >> 2435258

Lectin histochemistry and ultrastructure of kidneys from patients with I-cell disease.

M Castagnaro, J Alroy, A A Ucci, R Jaffe.   

Abstract

The undegraded stored material in I-cell disease (ICD) includes mucopolysaccharides, lipids, and oligosaccharides. We used ten different lectins as histochemical probes to identify specific carbohydrate residues in stored materials, and electron microscopy to examine the morphology of abnormally stored material in kidneys from two patients with ICD. In both cases, all the glomerular epithelial cells (ie, podocytes), endothelial cells, and renal tubular cells were enlarged and vacuolated. Ultrastructural studies revealed both fibrillogranular material and lamellated membrane structures in the vacuoles. The cytoplasm of affected cells stained with Concanavalia ensiformis agglutinin, wheat-germ agglutinin, and succinylated-wheat-germ agglutinin, but no corresponding control cells stained with lectins. The latter findings indicate an accumulation of N-linked oligosaccharides containing alpha-mannosyl, beta-N-acetylglucosaminyl, and sialyl residues in renal cells affected by ICD.

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Year:  1987        PMID: 2435258

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  2 in total

1.  Lectin histochemistry of an ovine lysosomal storage disease with deficiencies of beta-galactosidase and alpha-neuraminidase.

Authors:  R D Murnane; A J Ahern-Rindell; D J Prieur
Journal:  Am J Pathol       Date:  1989-10       Impact factor: 4.307

Review 2.  Proteinuria in a child with sialidosis: case report and histological studies.

Authors:  C E Kashtan; T E Nevins; Z Posalaky; R L Vernier; A J Fish
Journal:  Pediatr Nephrol       Date:  1989-04       Impact factor: 3.714

  2 in total

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