| Literature DB >> 17965825 |
Ikuo Kawashima1,2, Kazuhiko Watabe3, Youichi Tajima1,2, Tomoko Fukushige4, Tamotsu Kanzaki4, Takuro Kanekura4, Kanako Sugawara5, Naho Ohyanagi5, Toshihiro Suzuki5, Tadayasu Togawa5, Hitoshi Sakuraba6,7.
Abstract
Peripheral neuropathy is one of the important manifestations of Fabry disease. Enzyme replacement therapy with presently available recombinant alpha-galactosidases does not always improve the Fabry neuropathy. But the reason has not been determined yet. We established a Schwann cell line from Fabry mice, characterized it, and then examined the uptake of alpha-galactosidase by cells and its effect on the degradation of accumulated substrate. The cells exhibited a distinct Schwann cell morphology and biochemical phenotype (alpha-Galactosidase activity was deficient, and numerous cytoplasmic inclusion bodies were present in the cells). A recombinant alpha-galactosidase added to the culture medium was incorporated into the cultured Fabry Schwann cells dose dependently. But the increase in cell-associated enzyme activity was less than that in the cases of human and mouse Fabry fibroblasts. The administration of a high dose of the enzyme improved the pathological changes in cells, although a low dose of it did not. Cellular uptake of the enzyme was strongly inhibited in the presence of mannose 6-phosphate. This suggests that the enzyme is incorporated via cation-independent mannose 6-phosphate receptors in Schwann cells. The low expression of cation-independent mannose 6-phosphate receptors in Schwann cells must be one of the reasons their uptake of the present enzymes was low. The administration of a high dose of the enzyme or the development of an enzyme containing many mannose 6-phosphate residues is required to improve Fabry neuropathy.Entities:
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Year: 2007 PMID: 17965825 DOI: 10.1007/s10038-007-0210-x
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172