Diagnosis of arylsulfatase A deficiency in intact cultured cells using a fluorescent derivative of cerebroside sulfate
- 1 April 1987
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 31 (4) , 211-217
- https://doi.org/10.1111/j.1399-0004.1987.tb02798.x
Abstract
A fluorescent derivative of cerebroside sulfate (12-(1-pyrene)dodecanoyl-sphingosylgalactosyl-0-3-sulfate (P12-sulfatide)) has been synthesized as a potential substrate for the determination of cerebroside sulfatidase (or arylsulfatase A) activity. It was administered into cultured human skin fibroblasts and thereby utilized for the diagnosis of arylsulfatase A deficiency. Cultured skin fibroblasts from normal individuals and healthy persons suffering from a pseudoarylsulfatase A deficiency (PD) degraded the P12-sulfatide, while in cells derived from a metachromatic leukodystrophy (MLD) patient it remained essentially intact. This contrasts with in vitro determinations of enzymatic activity, where the MLD or PD-derived arylsulfatase A exhibit similar deficiency, in spite of a profoundly different clinical course. Administration of the fluorescent sulfatide into the intact cells permitted a sensitive and rapid diagnosis of MLD and its distinction from the PD-phenomenon. This might be of particular importance for cases in which a rapid diagnosis is required and for prenatal diagnosis of fetuses from families afflicted with both MLD and pseudo-deficiency mutant genes.Keywords
This publication has 18 references indexed in Scilit:
- A variant form of metachromatic leucodystrophy in a patient suffering from another congenital degenerative neurological diseaseActa Neurologica Scandinavica, 2009
- Metachromatic leukodystrophy manifesting as a schizophrenic disorder: Computed tomographic correlationAnnals of Neurology, 1985
- Non‐progressive psychomotor retardation in a child with severe deficiency of arylsulphatase A activityClinical Genetics, 1984
- Deficiency of lysosomal hydrolases in apparently healthy individualsAmerican Journal of Medical Genetics, 1983
- Problems in the clinical interpretation of arylsulfatase A deficiencyAmerican Journal of Medical Genetics, 1981
- Intracellular Localization of Exogenous β‐Glucuronidase in Cultured Skin FibroblastsEuropean Journal of Biochemistry, 1979
- Low arylsulphatase A activity in a family without metachromatic leukodystrophyClinical Genetics, 1978
- Cerebroside sulfate hydrolysis by fibroblasts from a parent with metachromatic leukodystrophyThe Journal of Pediatrics, 1978
- An efficient method for modulation of cholesterol level in cell membranesFEBS Letters, 1978
- The assay of arylsulphatases A and B in human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1959