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• W2744609562 startingPage "375" @default.
• W2744609562 abstract "The brain ventricular system (BVS) consists of brain ventricles and channels connecting ventricles filled with cerebrospinal fluid (CSF). The disturbance of CSF flow has been linked to neurodegenerative disease including hydrocephalus, which manifests itself as an abnormal expansion of BVS. This relatively common developmental disorder has been observed in human and domesticated animals and linked to functional deficiency of various cells lineages facing BVS, including the choroid plexus or ependymal cells that generate CSF or the ciliated cells that cilia beating generates CSF flow. To understand the underlying causes of hydrocephalus, several animal models were developed, including rodents (mice, rat, and hamster) and zebrafish. At another side of a spectrum of BVS anomalies there is the slit-ventricle syndrome, which develops due to insufficient inflation of BVS. Recent advances in functional genetics of zebrafish brought to light novel genetic elements involved in development of BVS and circulation of CSF. This review aims to reveal common elements of morphologically different BVS of zebrafish as a typical representative of teleosts and other vertebrates and illustrate useful features of the zebrafish model for studies of BVS. Along this line, recent analyses of the two novel zebrafish mutants affecting different subunits of the potassium voltage-gated channels allowed to emphasize an important functional convergence of the evolutionarily conserved elements of protein transport essential for BVS development, which were revealed by the zebrafish and mouse studies." @default.
• W2744609562 created "2017-08-17" @default.
• W2744609562 creator A5023303739 @default.
• W2744609562 date "2017-08-05" @default.
• W2744609562 modified "2023-10-16" @default.
• W2744609562 title "Development of brain ventricular system" @default.
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• W2744609562 doi "https://doi.org/10.1007/s00018-017-2605-y" @default.
• W2744609562 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5765195" @default.
• W2744609562 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28780589" @default.
• W2744609562 hasPublicationYear "2017" @default.
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