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The Neuroepithelium Disruption Could Generate Autoantibodies against AQP4 and Cause Neuromyelitis Optica and Hydrocephalus
Author(s) -
Leandro Castañeyra-Ruiz,
Ibrahim González-Marrero,
Agustín Castañeyra-Ruiz,
Juan M. González-Toledo,
María Castañeyra-Ruiz,
Francisco J. Pérez-Moltó,
Emilia M. Carmona-Calero,
Agustín Castañeyra-Perdomo
Publication year - 2014
Publication title -
international scholarly research notices
Language(s) - English
Resource type - Journals
ISSN - 2356-7872
DOI - 10.1155/2014/580572
Subject(s) - neuromyelitis optica , aquaporin 4 , medicine , cerebrospinal fluid , hydrocephalus , pathology , myelitis , neuroepithelial cell , subventricular zone , antibody , immunology , spinal cord , biology , radiology , stem cell , progenitor cell , genetics , neural stem cell , psychiatry
Neuromyelitis optica is an inflammatory disease characterized by neuritis and myelitis of the optic nerve. Its physiopathology is connected with the aquaporin-4 water channel, since antibodies against aquaporin-4 have been found in the cerebrospinal fluid and blood of neuromyelitis optica patients. The seropositivity for aquaporin-4 antibodies is used for the diagnosis of neuromyelitis optica or neuromyelitis optica spectrum disease. On the other hand, aquaporin-4 is expressed in astrocyte feet in the brain-blood barrier and subventricular zones of the brain ventricles. Aquaporin-4 expression is high in cerebrospinal fluid in hydrocephalus. Furthermore, neuroepithelial denudation precedes noncommunicating hydrocephalus and this neuroepithelial disruption could allow aquaporin-4 to reach anomalous brain areas where it is unrecognized and induce the generation of aquaporin-4 antibodies which could cause the neuromyelitis optica and certain types of hydrocephalus.

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