Abstract
In order to evaluate the mechanisms leading to neuropathology in Mucopolysaccharidosis type IIIA (MPS-IIIA, Sanfilippo syndrome), we have harvested and cultured primary neural cells isolated from the cerebellum of newborn and adult MPS-IIIA and unaffected mice. Cell viability and plating efficiency were comparable for brain tissue obtained from either newborn or adult MPS-IIIA and unaffected mice. Cultures (newborn and adult) comprised a mixed brain cell population including astrocytes, oligodendrocytes, and neurons. Newborn MPS-IIIA cells contained inclusions and vacuoles consistent with the pathology present in affected brain tissue. Newborn and adult MPS-IIIA brain cells had approximately 5-7% of the sulfamidase activity present in primary neural cells cultured from unaffected newborn and adult mice. In addition, high levels of glucosamine-N-sulfate[α-1,4]hexuronic acid, a heparan sulfate-derived disaccharide, were detected in both newborn and adult MPS-IIIA brain cells. These results suggest that the primary MPS-IIIA brain cells exhibit characteristics of MPS-IIIA phenotype at the histopathological and biochemical level in culture.
Original language | English |
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Pages (from-to) | 949-959 |
Number of pages | 11 |
Journal | Cellular and Molecular Neurobiology |
Volume | 28 |
Issue number | 7 |
DOIs | |
Publication status | Published or Issued - Nov 2008 |
Keywords
- Brain cell culture
- Heparan sulfate
- Lysosomal storage disorder
- Mouse model
- Mucopolysaccharidosis type IIIA
- Pathology
- Sulfamidase
ASJC Scopus subject areas
- Cellular and Molecular Neuroscience
- Cell Biology