Literature DB >> 6275710

Alterations in the proximal nephron of beige mice with the Chédiak-Higashi syndrome.

M Eguchi, K C Poon, S S Spicer.   

Abstract

The proximal nephron of C57 beige mice with a genetic defect analagous to the Chédiak-Higashi syndrome (CHS) has been compared with that of normal C57 black mice. The concanavalin A-horseradish peroxidase (Con A-HRP) technique stained the brush border of the proximal straight tubule heavily in black mice and weakly in beige mice. In beige mice this method stained the brush border of the proximal convoluted tubules weakly and the brush border of the proximal straight tubules only negligibly. Periodic acid-Schiff staining showed no such difference between beige and black mice but revealed an increase distally in the size of the CHS inclusions in the proximal straight tubule of beige mice. Immunostaining visualized abundant lysozyme in the first portion of the proximal nephron but none in the more distal segments of beige and black mice alike. At the ultrastructural level, the proximal convoluted tubules of black mice contained two morphologic types of heterophagosomes, which apparently differed in accord with the stage of their development. Proximal straight tubules contained morphologically different heterophagic bodies. The mature stages of these heterophagosomes were greatly enlarged in CHS mice. With the periodic acid-thiocarbohydrazide-silver proteinate (PA-T-SP) method for localizing glycoprotein ultrastructurally, the microvillar brush border, apical invaginations of the plasmalemma, Golgi cisternae, and lysosomal inclusions stained selectively in the proximal nephron in both strains. The proximal straight nephron of beige mice after staining with the PA-T-SP method appeared depleted of the strongly reactive apical invaginations in some areas, particularly where large heterophagosomes bordered the apical plasmalemma. The enlarged secondary lysosomes of heterophagic origin in beige mice varied in showing both diffuse and focal PA-T-SP reactivity. Lysosomal acid phosphatase activity appeared decreased, and peroxisomes were normal in size but increased in number in the proximal nephron of beige mice.

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Year:  1982        PMID: 6275710      PMCID: PMC1915971     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  32 in total

1.  Studies on microperoxisomes. II. A cytochemical method for light and electron microscopy.

Authors:  A B Novikoff; P M Novikoff; C Davis; N Quintana
Journal:  J Histochem Cytochem       Date:  1972-12       Impact factor: 2.479

2.  Ultrastructure of bone marrow granulocytes in normal mink and mink with the homolog of the Chediak-Higashi trait of humans. I. Origin of the abnormal granules present in the neutrophils of mink with the C-HS trait.

Authors:  W C Davis; S S Spicer; W B Greene; G A Padgett
Journal:  Lab Invest       Date:  1971-04       Impact factor: 5.662

3.  Ultrastructure of cells in bone marrow and peripheral blood of normal mink and mink with the homologue of the Chediak-Higashi trait of humans. II. Cytoplasmic granules in eosinophils, basophils, mononuclear cells and platelets.

Authors:  W C Davis; S S Spicer; W B Greene; G A Padgett
Journal:  Am J Pathol       Date:  1971-06       Impact factor: 4.307

4.  Observations on the segmentation of the proximal tubule in the rat kidney. Comparison of results from phase contrast, fluorescence and electron microscopy.

Authors:  A B Maunsbach
Journal:  J Ultrastruct Res       Date:  1966-10

5.  Ultrastructural visualization of cellular carbohydrate components by means of concanavalin A.

Authors:  W Bernhard; S Avrameas
Journal:  Exp Cell Res       Date:  1971-01       Impact factor: 3.905

6.  The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique.

Authors:  R C Graham; M J Karnovsky
Journal:  J Histochem Cytochem       Date:  1966-04       Impact factor: 2.479

7.  Abnormal bactericidal, metabolic, and lysosomal functions of Chediak-Higashi Syndrome leukocytes.

Authors:  R K Root; A S Rosenthal; D J Balestra
Journal:  J Clin Invest       Date:  1972-03       Impact factor: 14.808

8.  Defective function of renal lysosomes in mice with the Chediak-Higashi syndrome.

Authors:  D J Prieur; W C Davis; G A Padgett
Journal:  Am J Pathol       Date:  1972-05       Impact factor: 4.307

9.  Distribution of peroxisomes (microbodies) in the nephron of the rat: a cytochemical study.

Authors:  M E Beard; A B Novikoff
Journal:  J Cell Biol       Date:  1969-08       Impact factor: 10.539

10.  Changes in fine structure and acid phosphatase localization in rat thyroid cells following thyrotropin administration.

Authors:  B K Wetzel; S S Spicer; S H Wollman
Journal:  J Cell Biol       Date:  1965-06       Impact factor: 10.539

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  1 in total

1.  Glycoconjugates in normal human kidney. A histochemical study using 13 biotinylated lectins.

Authors:  L D Truong; V T Phung; Y Yoshikawa; C A Mattioli
Journal:  Histochemistry       Date:  1988
  1 in total

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