ALTERATIONS IN THE PROXIMAL NEPHRON OF BEIGE MICE WITH THE CHEDIAK-HIGASHI-SYNDROME
- 1 January 1982
- journal article
- research article
- Vol. 106 (1) , 95-109
Abstract
The proximal nephron of C57 beige mice with a genetic defect analogous to the Chediak-Higashi syndrome (CHS) [in humans] was 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 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 1st 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 2 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.This publication has 32 references indexed in Scilit:
- STUDIES ON MICROPEROXISOMES II. A CYTOCHEMICAL METHOD FOR LIGHT AND ELECTRON MICROSCOPYJournal of Histochemistry & Cytochemistry, 1972
- Defective function of renal lysosomes in mice with the Chediak-Higashi syndrome.1972
- Abnormal Bactericidal, Metabolic, and Lysosomal Functions of Chediak-Higashi Syndrome LeukocytesJournal of Clinical Investigation, 1972
- 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.1971
- 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.1971
- Ultrastructural visualization of cellular carbohydrate components by means of concanavalin AExperimental Cell Research, 1971
- DISTRIBUTION OF PEROXISOMES (MICROBODIES) IN THE NEPHRON OF THE RATThe Journal of cell biology, 1969
- Observations on the segmentation of the proximal tubule in the rat kidneyJournal of Ultrastructure Research, 1966
- THF EARLY STAGES OF ABSORPTION OF INJECTED HORSERADISH PEROXIDASE IN THE PROXIMAL TUBULES OF MOUSE KIDNEY: ULTRASTRUCTURAL CYTOCHEMISTRY BY A NEW TECHNIQUEJournal of Histochemistry & Cytochemistry, 1966
- CHANGES IN FINE STRUCTURE AND ACID PHOSPHATASE LOCALIZATION IN RAT THYROID CELLS FOLLOWING THYROTROPIN ADMINISTRATIONThe Journal of cell biology, 1965