<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang B</submitter><funding>NIBIB NIH HHS</funding><funding>NEI NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>15280-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2397463</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>283(22)</volume><pubmed_abstract>Aquaporin-4 (AQP4) is a water transport protein expressed in glial cell plasma membranes, including glial cell foot processes lining the blood-brain barrier. AQP4 deletion in mice reduces cytotoxic brain edema produced by different pathologies. To determine whether AQP4 is rate-limiting for brain water accumulation and whether altered AQP4 expression, as occurs in various pathologies, could have functional importance, we generated mice that overexpressed AQP4 in brain glial cells by a transgenic approach using the glial fibrillary acid protein promoter. Overexpression of AQP4 protein in brain by approximately 2.3-fold did not affect mouse survival, appearance, or behavior, nor did it affect brain anatomy or intracranial pressure (ICP). However, following acute water intoxication produced by intraperitoneal water injection, AQP4-overexpressing mice had an accelerated progression of cytotoxic brain swelling, with ICP elevation of 20 +/- 2 mmHg at 10 min, often producing brain herniation and death. In contrast, ICP elevation was 14 +/- 2 mmHg at 10 min in control mice and 9.8 +/- 2 mmHg in AQP4 knock-out mice. The deduced increase in brain water content correlated linearly with brain AQP4 protein expression. We conclude that AQP4 expression is rate-limiting for brain water accumulation, and thus, that altered AQP4 expression can be functionally significant.</pubmed_abstract><journal>The Journal of biological chemistry</journal><pubmed_title>Glial cell aquaporin-4 overexpression in transgenic mice accelerates cytotoxic brain swelling.</pubmed_title><pmcid>PMC2397463</pmcid><funding_grant_id>EY 13574</funding_grant_id><funding_grant_id>EB 00415</funding_grant_id><funding_grant_id>HL 73856</funding_grant_id><funding_grant_id>DK 72517</funding_grant_id><funding_grant_id>DK 35124</funding_grant_id><funding_grant_id>HL 59198</funding_grant_id><pubmed_authors>Zador Z</pubmed_authors><pubmed_authors>Verkman AS</pubmed_authors><pubmed_authors>Yang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Glial cell aquaporin-4 overexpression in transgenic mice accelerates cytotoxic brain swelling.</name><description>Aquaporin-4 (AQP4) is a water transport protein expressed in glial cell plasma membranes, including glial cell foot processes lining the blood-brain barrier. AQP4 deletion in mice reduces cytotoxic brain edema produced by different pathologies. To determine whether AQP4 is rate-limiting for brain water accumulation and whether altered AQP4 expression, as occurs in various pathologies, could have functional importance, we generated mice that overexpressed AQP4 in brain glial cells by a transgenic approach using the glial fibrillary acid protein promoter. Overexpression of AQP4 protein in brain by approximately 2.3-fold did not affect mouse survival, appearance, or behavior, nor did it affect brain anatomy or intracranial pressure (ICP). However, following acute water intoxication produced by intraperitoneal water injection, AQP4-overexpressing mice had an accelerated progression of cytotoxic brain swelling, with ICP elevation of 20 +/- 2 mmHg at 10 min, often producing brain herniation and death. In contrast, ICP elevation was 14 +/- 2 mmHg at 10 min in control mice and 9.8 +/- 2 mmHg in AQP4 knock-out mice. The deduced increase in brain water content correlated linearly with brain AQP4 protein expression. We conclude that AQP4 expression is rate-limiting for brain water accumulation, and thus, that altered AQP4 expression can be functionally significant.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 May</publication><modification>2025-04-04T19:30:30.934Z</modification><creation>2019-03-27T00:15:17Z</creation></dates><accession>S-EPMC2397463</accession><cross_references><pubmed>18375385</pubmed><doi>10.1074/jbc.M801425200</doi><doi>10.1074/jbc.m801425200</doi></cross_references></HashMap>