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QUANTITATIVE CORRELATION BETWEEN THE RESIDUAL ACTIVITY OF BETA-HEXOSAMINIDASE-A AND ARYLSULFATASE-A AND THE SEVERITY OF THE RESULTING LYSOSOMAL STORAGE DISEASE
Author(s): LEINEKUGEL P, MICHEL S, CONZELMANN E, SANDHOFF K
Source: HUMAN GENETICS    Volume: 88    Issue: 5    Pages: 513-523    Published: MAR 1992  
Times Cited: 162     References: 42     
Abstract: A previously suggested model for the correlation between residual activity of a lysosomal enzyme and the turnover rate of its substrate(s) has been extended to a discussion of substrate accumulation rates in individual cells and whole organs. With these considerations, much of the observed variability in age of onset and clinical phenotype, as well as the phenomenon of pseudo-deficiency, can be understood as the consequences of small differences in the residual activity of the affected enzyme. In order to experimentally verify the basic assumptions on which this model rests, studies were performed in cell culture. The radiolabeled substrates ganglioside G(M2) and sulfatide were added to cultures of skin fibroblasts with different activities of beta-hexosaminidase A or arylsulfatase A, respectively, and their uptake and turnover measured. In both series of experiments, the correlation between residual enzyme activity and the turnover rate of the substrate was essentially as predicted: degradation increased steeply with residual activity, to reach the control level at a residual activity of approximately 10-15% of normal. All cells with an activity above this critical threshold had a normal turnover. Comparison of the results of these feeding studies with the clinical status of the donor of each cell line basically confirmed our notions but also revealed the limitations of the cell culture approach.
Document Type: Article
Language: English
Addresses:
1. UNIV BONN, INST ORGAN CHEM & BIOCHEM, GERHARD DOMAGK STR 1, W-5300 BONN 1, GERMANY
Publisher: SPRINGER VERLAG, 175 FIFTH AVE, NEW YORK, NY 10010
Subject Category: Genetics & Heredity
IDS Number: HJ345
ISSN: 0340-6717
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