Apparently normal extracellular acidic alpha-mannosidase in fibroblast cultures from patients with mannosidosis

• Published in: American journal of human genetics Vol. 34; no. 1; pp. 100 - 111
• Main Authors: Ben-Yoseph, Y, DeFranco, C L, Charrow, J, Hahn, L C, Nadler, H L
• Format: Journal Article
• Language: English
• Published: United States 01.01.1982
• Subjects: alpha-Mannosidase; Carbohydrate Metabolism, Inborn Errors - enzymology; Carbohydrate Metabolism, Inborn Errors - genetics; Cells, Cultured; Culture Media; Fibroblasts - enzymology; Hot Temperature; Humans; Kinetics; Lysosomes - enzymology; Mannose - metabolism; Mannosidases - deficiency; Mannosidases - metabolism; Mutation
• ISSN: 0002-9297; 1537-6605

Fibroblasts from patients with mannosidosis, cultured in medium supplemented with fetal calf serum from which acidic alpha-mannosidase (alpha-D-mannoside mannohydrolase, E.C.3.2.1.24) has been removed, secreted a normal amount of apparently unaffected acidic alpha-mannosidase into fetal calf serum-free medium. Both the intracellular and extracellular acidic alpha-mannosidase activities were completely precipitated by antiserum to placenta alpha-mannosidase B. In contrast to the heat-lability of the intracellular acidic alpha-mannosidase and its low affinity for artificial mannoside substrate, the extracellular enzyme exhibited both normal thermostability and normal kinetics. Mixing experiments with the intercellular enzymes suggested that the decreased activity in the patients' fibroblasts is not the effect of an inhibitor or absence of an activator. However, incubation of the mannosidosis extracellular enzyme with either normal or patient cell lysate resulted in a partial loss of activity, whereas an additive value was observed with the normal extracellular enzyme. In contrast to normal culture medium, the medium from mannosidosis cell culture was unable to enhance the rate of reduction of intracellular radioactivity in mucolipidosis type II fibroblasts precultured in the presence of radiolabeled mannose. These findings suggest that the defect in mannosidosis is expressed only after the enzyme has been delivered to lysosomes and presumably undergone some form of processing there.