Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblasts.

Abstract

High-titre stocks of an amphotropic retrovirus, constructed so as to express a full-length cDNA encoding the human lysosomal enzyme N-acetylgalactosamine-4-sulphatase (4-sulphatase) from the cytomegalovirus immediate early promoter, were used to infect skin fibroblasts from a clinically severe mucopolysaccharidosis type VI (MPS VI) patient. The infected MPS VI cells showed correction of the enzymic defect with the enzyme being expressed at high levels and in the correct subcellular compartment. Surprisingly this did not result in correction of glycosaminoglycan turnover as measured by accumulation of 35S in metabolically labelled cells. We demonstrate that this is apparently caused by an induced reduction of the activities of other lysosomal sulphatases, presumably due to competition for a sulphatase-specific processing mechanism by the over-expressed 4-sulphatase. The level of steroid sulphatase, which is a microsomal sulphatase, was also reduced. Infection of skin fibroblasts from a second, clinically mildly affected, MPS VI patient with the same virus also resulted in no significant change in the level of glycosaminoglycan storage. However, in this case the cause of the observed phenomenon was less clear. These results are of obvious practical importance when considering gene therapy for a sulphatase deficiency such as MPS VI and also provide possible new avenues for exploration of the processes involved in sulphatase synthesis and genetically determined multiple sulphatase deficiency.

• Authors: D S Anson, V Muller, J Bielicki, G S Harper, J J Hopwood
• Journal: The Biochemical journal (Biochem J) Vol. 294 ( Pt 3) Pg. 657-62 (Sep 15 1993) ISSN: 0264-6021 [Print] England
• PMID: 8379921 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Glycosaminoglycans
• Recombinant Proteins
• Chondro-4-Sulfatase

Topics

• Chondro-4-Sulfatase (genetics, metabolism)
• Genetic Therapy
• Glycosaminoglycans (metabolism)
• Humans
• Lysosomes (enzymology)
• Mucopolysaccharidosis VI (enzymology)
• Recombinant Proteins (metabolism)
• Skin (enzymology)
• Transfection