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https://hdl.handle.net/2440/17363
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dc.contributor.author | Robinson, A. | - |
dc.contributor.author | Crawley, A. | - |
dc.contributor.author | Hopwood, J. | - |
dc.date.issued | 2005 | - |
dc.identifier.citation | Molecular Genetics and Metabolism, 2005; 85(3):203-212 | - |
dc.identifier.issn | 1096-7192 | - |
dc.identifier.issn | 1096-7206 | - |
dc.identifier.uri | http://hdl.handle.net/2440/17363 | - |
dc.description.abstract | Alpha-mannosidosis is a lysosomal storage disorder characterised by the lysosomal accumulation of mannose-containing oligosaccharides and a range of pathological consequences, caused by a deficiency of the lysosomal enzyme alpha-mannosidase. One of the major features of alpha-mannosidosis is progressive neurological decline, for which there is no safe and effective treatment. Implantation of stem cells into the central nervous system has been proposed as a potential therapy for these disorders. We report the construction and characterisation of mouse embryonic stem cell lines for the sustained over-expression of recombinant human lysosomal alpha-mannosidase (rhalphaM). Two vectors (involving recombinant human alpha-mannosidase expression driven by either the chicken beta-actin promoter/CMV enhancer or by the elongation factor 1-alpha promoter) were constructed and used to transfect mouse D3 embryonic stem cells. Selected clonal cell lines were isolated and tested to evaluate their expression of recombinant human alpha-mannosidase. Stem cell clones transfected with the chicken beta-actin promoter/CMV enhancer maintained rhalphaM expression levels throughout differentiation. This expression was not markedly elevated above background. In contrast, the vector incorporating the elongation factor 1-alpha promoter facilitated substantial over-expression of alpha-mannosidase when analysed out to 21 days of differentiation in stably transfected cell lines. The highest expressing cell line was found to qualitatively retain a similar differentiation potential to untransfected cells, and to secrete alpha-mannosidase that could mediate a reduction in the level of oligosaccharides stored by human alpha-mannosidosis skin fibroblasts. These results suggest potential for the use of this cell line for investigation of a stem cell therapy approach to treat alpha-mannosidosis. | - |
dc.language.iso | en | - |
dc.publisher | Academic Press Inc Elsevier Science | - |
dc.source.uri | http://dx.doi.org/10.1016/j.ymgme.2005.03.005 | - |
dc.subject | Cell Line | - |
dc.subject | Stem Cells | - |
dc.subject | Animals | - |
dc.subject | Humans | - |
dc.subject | Mice | - |
dc.subject | alpha-Mannosidosis | - |
dc.subject | alpha-Mannosidase | - |
dc.subject | Mannosephosphates | - |
dc.subject | Stem Cell Transplantation | - |
dc.subject | Transfection | - |
dc.subject | Gene Expression | - |
dc.subject | Up-Regulation | - |
dc.title | Over-expression of human lysosomal -mannosidae in mouse embryonic stem cells | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1016/j.ymgme.2005.03.005 | - |
pubs.publication-status | Published | - |
Appears in Collections: | Aurora harvest 2 Paediatrics publications |
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