<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>42(3)</volume><submitter>Lu H</submitter><pubmed_abstract>Aquaporin 4 (AQP4) is highly expressed on astrocytes and is critical for controlling brain water transport in neurological diseases. Tumor necrosis factor (TNF)-α is a common cytokine found in disease microenvironment. The aim of the present study was to determine whether TNF-α can regulate the expression of AQP4 in astrocytes. Primary astrocyte cultures were treated with different concentrations of TNF-α and the cell viability was assessed through cell counting kit-8 (CCK-8) assay and AQP4 expression was detected by qPCR, Western blots, and immunofluorescence assays. The activation of nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) pathway was detected by Western blot. Further, dual-luciferase reporting system and chromatin immunoprecipitation (ChIP) were used to detect</pubmed_abstract><journal>Bioscience reports</journal><pagination>BSR20212224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8935387</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TNF-α induces AQP4 overexpression in astrocytes through the NF-κB pathway causing cellular edema and apoptosis.</pubmed_title><pmcid>PMC8935387</pmcid><pubmed_authors>Lu H</pubmed_authors><pubmed_authors>Ai L</pubmed_authors><pubmed_authors>Zhang B</pubmed_authors></additional><is_claimable>false</is_claimable><name>TNF-α induces AQP4 overexpression in astrocytes through the NF-κB pathway causing cellular edema and apoptosis.</name><description>Aquaporin 4 (AQP4) is highly expressed on astrocytes and is critical for controlling brain water transport in neurological diseases. Tumor necrosis factor (TNF)-α is a common cytokine found in disease microenvironment. The aim of the present study was to determine whether TNF-α can regulate the expression of AQP4 in astrocytes. Primary astrocyte cultures were treated with different concentrations of TNF-α and the cell viability was assessed through cell counting kit-8 (CCK-8) assay and AQP4 expression was detected by qPCR, Western blots, and immunofluorescence assays. The activation of nuclear factor κ-light-chain-enhancer of activated B cells (NF-κB) pathway was detected by Western blot. Further, dual-luciferase reporting system and chromatin immunoprecipitation (ChIP) were used to detect</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T20:23:40.547Z</modification><creation>2025-04-04T20:23:40.547Z</creation></dates><accession>S-EPMC8935387</accession><cross_references><pubmed>35260880</pubmed><doi>10.1042/BSR20212224</doi></cross_references></HashMap>