| Literature DB >> 27751903 |
Gry Fluge Vindedal1, Anna E Thoren2, Vidar Jensen2, Arne Klungland3, Yong Zhang4, Michael J Holtzman4, Ole Petter Ottersen5, Erlend A Nagelhus6.
Abstract
There is a constitutive production of water in brain. The efflux routes of this excess water remain to be identified. We used basal brain water content as a proxy for the capacity of water exit routes. Basal brain water content was increased in mice with a complete loss of aquaporin-4 (AQP4) water channels (global Aqp4-/- mice), but not in mice with a selective removal of perivascular AQP4 or in a novel mouse line with a selective deletion of ependymal AQP4 (Foxj1-Cre:Aqp4flox/flox mice). Unique for the global Aqp4-/- mice is the loss of the AQP4 pool subjacent to the pial membrane. Our data suggest that water accumulates in brain when subpial AQP4 is missing, pointing to a critical role of this pool of water channels in brain water exit. Copyright ÂEntities:
Keywords: AQP4; Alpha-syntrophin; Aquaporin; Astrocytes; Brain edema; CSF; Cerebrospinal fluid; Endfeet; Ependyma; Extracellular space; Foxj1; Glia; Glymphatic; Interstitial fluid; Neuron-glial; Paravascular; Water homeostasis
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Year: 2016 PMID: 27751903 PMCID: PMC5157926 DOI: 10.1016/j.mcn.2016.10.004
Source DB: PubMed Journal: Mol Cell Neurosci ISSN: 1044-7431 Impact factor: 4.314