» Articles » PMID: 990381

Deficit in Neuraminidase Associated with Mucolipidosis II (I-cell Disease)

Overview
Journal Biomedicine
Specialty Biology
Date 1976 Sep 30
PMID 990381
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Using a tritiated sialyloligosaccharide as a substrate, the authors showed that mucolipidosis II is characterized by a lack of neuraminidase activity in leucocytes, while the other acidic hydrolases activities are normal. According to Ashwell, terminal galactose is the required signal for glycoproteins uptake by the cells. Thus, a neuraminidase deficit may explain the increase of sialylated hydrolases activities in the plasma and the non-recognition of these enzymes by cultured fibroblasts.

Citing Articles

Chick embryo fibroblasts produce two forms of hyaluronidase.

Orkin R, Toole B J Cell Biol. 1980; 85(2):248-57.

PMID: 7372707 PMC: 2110628. DOI: 10.1083/jcb.85.2.248.


Influence of sialic acid on cell surface properties in I-cell disease fibroblasts.

Vladutiu G, Fike R, Amigone V In Vitro. 1981; 17(7):588-92.

PMID: 7327591 DOI: 10.1007/BF02618456.


Cellular localization of neuraminidases in cultured human fibroblasts.

Zeigler M, Bach G Biochem J. 1981; 198(3):505-8.

PMID: 7326018 PMC: 1163295. DOI: 10.1042/bj1980505.


Cherry-red spot myoclonus syndrome and alpha-neuraminidase deficiency: neurophysiological, pharmacological and biochemical study in an adult.

Franceschetti S, Uziel G, Di Donato S, Caimi L, Avanzini G J Neurol Neurosurg Psychiatry. 1980; 43(10):934-40.

PMID: 6777461 PMC: 490715. DOI: 10.1136/jnnp.43.10.934.


I-cell disease. A hypothesis for the structure of the carbohydrate recognition site on beta-D-N-acetylhexosaminidase.

Vladutiu G Biochem J. 1978; 171(2):509-12.

PMID: 656062 PMC: 1183985. DOI: 10.1042/bj1710509.