The study supports a role for myelin-associated glycoprotein (MAG) in the maintenance of myelin at the paranodal regions, as its deficiency leads to tomacula formation via redundant myelin foldings.
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Hypothesis-generating for MAG in paranodal myelin maintenance; human studies needed before clinical translation.
The pathogenesis of tomacula in mice with a null mutation of the myelin-associated glycoprotein (MAG) gene is not well understood. This study, using a novel teased nerve fiber technique, demonstrates that tomacula in MAG-deficient mice are formed by redundant myelin infoldings and outfoldings in the paranodal regions as early as 4 weeks after birth and increase in size and frequency with age. Although tomacula show degenerative changes with increasing age, there was no significant evidence of demyelination/remyelination. Longitudinal sections of normal teased nerve fibers show early redundant myelin foldings in externally normal paranodal regions. These data and the absence of internodal tomacula support a role for MAG in the maintenance of myelin at the paranodal regions.
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Cai et al. (2002) studied this question.
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