In:
Journal of Negative Results in BioMedicine, Springer Science and Business Media LLC, Vol. 6, No. 1 ( 2007-12)
Abstract:
Sandhoff disease is an inherited lysosomal storage disease caused by a mutation in the gene for the β-subunit ( Hexb gene) of β-hexosaminidase A (αβ) and B (ββ). The β-subunit together with the GM2 activator protein catabolize ganglioside GM2. This enzyme deficiency results in GM2 accumulation primarily in the central nervous system. To investigate how abnormal GM2 catabolism affects the peripheral nervous system in a mouse model of Sandhoff disease ( Hexb-/- ), we examined the electrophysiology of dissected sciatic nerves, structure of central and peripheral myelin, and lipid composition of the peripheral nervous system. Results We detected no significant difference in signal impulse conduction velocity or any consistent change in the frequency-dependent conduction slowing and failure between freshly dissected sciatic nerves from the Hexb +/- and Hexb -/- mice. The low-angle x-ray diffraction patterns from freshly dissected sciatic and optic nerves of Hexb +/- and Hexb -/- mice showed normal myelin periods; however, Hexb -/- mice displayed a ~10% decrease in the relative amount of compact optic nerve myelin, which is consistent with the previously established reduction in myelin-enriched lipids (cerebrosides and sulfatides) in brains of Hexb-/- mice. Finally, analysis of lipid composition revealed that GM2 content was present in the sciatic nerve of the Hexb -/- mice (undetectable in Hexb +/-). Conclusion Our findings demonstrate the absence of significant functional, structural, or compositional abnormalities in the peripheral nervous system of the murine model for Sandhoff disease, but do show the potential value of integrating multiple techniques to evaluate myelin structure and function in nervous system disorders.
Type of Medium:
Online Resource
ISSN:
1477-5751
DOI:
10.1186/1477-5751-6-8
Language:
English
Publisher:
Springer Science and Business Media LLC
Publication Date:
2007
detail.hit.zdb_id:
2091480-5
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