Dec 1, 1975

Defective lysosomal enzyme secretion in kidneys of Chediak-Higashi (beige) mice

The Journal of Cell Biology
E J BrandtR T Swank

Abstract

The beige mouse is an animal model for the human Chediak-Higashi syndrome, a disease characterized by giant lysosomes in most cell types. In mice, treatment with androgenic hormones causes a 20-50-fold elevation in at least one kidney lysosomal enzyme, beta-glucuronidase. Beige mice treated with androgen had significantly higher kidney beta-glucuronidase, beta-galactosidase, and N-acetyl-beta-D-glucosaminidase (hexosaminidase) levels than normal mice. Other androgen-inducible enzymes and enzyme markers for the cytosol, mitochondria, and peroxisomes were not increased in kidney of beige mice. No significant lysosomal enzyme elevation was observed in five other organs of beige mice with or without androgen treatment, nor in kidneys of beige females not treated with androgen. Histochemical staining for glucuronidase together with subcellular fractionation showed that the higher glucuronidase content of beige mouse kidney is caused by a striking accumulation of giant glucuronidase-containing lysosomes in tubule cells near the corticomedullary boundary. In normal mice lysosomal enzymes are coordinately released into the lumen of the kidney tubules and appreciable amounts of lysosomal enzymes are present in the urine. Levels of urina...Continue Reading

Mentioned in this Paper

D-Amino Acid Dehydrogenase
Alcohol Oxidoreductases
Spleen
Succinate Dehydrogenase
Myocardium
Kidney
LYST
Exo-beta-D-Glucuronidase
Lysosomes
GUSB

About this Paper

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