Abstract

Background The hyh (hydrocephalus with hop gait) mouse carries a point mutation in alpha-SNAP protein and develops inherited hydrocephalus. Mutant mice are born with moderate hydrocephalus and a patent Sylvius aqueduct (SA). During the first postnatal week, SA obliterates and a severe hydrocephalus characterized by an enormous expansion of the dorsal third ventricle and of the collicular recess of the SA, develops. Interestingly, neither of these dilated cavities present spontaneous ventriculostomies. The aim of the present investigation was to elucidate some of the cellular phenomena occurring at the ventricular walls that allow such enormous ventricular dilatations.

Highlights

  • The hyh mouse carries a point mutation in alpha-SNAP protein and develops inherited hydrocephalus

  • Proliferative cells were found in two discrete ependymal regions of the dorsal walls of the third ventricle (3Vd) and the Sylvius aqueduct (SA) (SAd)

  • In mutant hyh mice, postnatal ependymogenesis occuring in 3Vd and SAd increased several fold

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Summary

Open Access

Address: 1Instituto de Histología y Patología, Universidad Austral de Chile, Valdivia, Chile and 2Departamento de Biología Celular, Universidad de Málaga, Spain. 51st Annual Meeting of the Society for Research into Hydrocephalus and Spina Bifida Meeting abstracts – A single PDF containing all abstracts in this Supplement is available here. http://www.biomedcentral.com/content/files/pdf/1743-8454-4-S1-info.pdf

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