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Clearance of activity‐evoked K + transients and associated glia cell swelling occur independently of AQP4 : A study with an isoform‐selective AQP4 inhibitor
Author(s) -
ToftBertelsen Trine Lisberg,
Larsen Brian Roland,
Christensen Sofie Kjellerup,
Khandelia Himanshu,
Waagepetersen Helle S.,
MacAulay Nanna
Publication year - 2021
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.23851
Subject(s) - extracellular , ependymal cell , aquaporin 4 , hippocampal formation , biology , microbiology and biotechnology , gene isoform , neuroglia , inhibitory postsynaptic potential , intracellular , biophysics , astrocyte , xenopus , neuroscience , central nervous system , biochemistry , gene
The mammalian brain consists of 80% water, which is continuously shifted between different compartments and cellular structures by mechanisms that are, to a large extent, unresolved. Aquaporin 4 (AQP4) is abundantly expressed in glia and ependymal cells of the mammalian brain and has been proposed to act as a gatekeeper for brain water dynamics, predominantly based on studies utilizing AQP4‐deficient mice. However, these mice have a range of secondary effects due to the gene deletion. An efficient and selective AQP4 inhibitor has thus been sorely needed to validate the results obtained in the AQP4 −/− mice to quantify the contribution of AQP4 to brain fluid dynamics. In AQP4‐expressing Xenopus laevis oocytes monitored by a high‐resolution volume recording system, we here demonstrate that the compound TGN‐020 is such a selective AQP4 inhibitor. TGN‐020 targets the tested species of AQP4 with an IC 50 of ~3.5 μM, but displays no inhibitory effect on the other AQPs (AQP1‐AQP9). With this tool, we employed rat hippocampal slices and ion‐sensitive microelectrodes to determine the role of AQP4 in glia cell swelling following neuronal activity. TGN‐020‐mediated inhibition of AQP4 did not prevent stimulus‐induced extracellular space shrinkage, nor did it slow clearance of the activity‐evoked K + transient. These data, obtained with a verified isoform‐selective AQP4 inhibitor, indicate that AQP4 is not required for the astrocytic contribution to the K + clearance or the associated extracellular space shrinkage.