<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liang M</submitter><funding>Xinjiang Production and Construction Corps</funding><funding>National Natural Science Foundation of China</funding><pagination>100981</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12925546</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>67(2)</volume><pubmed_abstract>In recent studies, acute physiological stress has been shown to enhance liver gluconeogenesis by activating β3-adrenergic receptor (ADRB3)-dependent interleukin-6 (IL-6) production in brown adipocytes, effectively fueling "fight or flight" responses. However, the specific molecular mechanism of this IL-6 production in an ADRB3-dependent manner is not fully understood. ADRB3 regulates multiple metabolic programs in adipose tissue, including thermogenesis, lipolysis, and glucose uptake, by activating cAMP-PKA-CREB signaling. Our previous studies revealed that the transcription factor Krüppel-like factor 7 (KLF7) transcriptionally induces IL-6 expression in white adipocytes. Using Klf7-adipocyte knockout mice, we showed that Klf7 is also required for ADRB3-induced IL-6 production during stres</pubmed_abstract><journal>Journal of lipid research</journal><pubmed_title>KLF7 induced ADRB3-dependent IL-6 production in brown adipocytes during stress.</pubmed_title><pmcid>PMC12925546</pmcid><funding_grant_id>2022ZD083</funding_grant_id><funding_grant_id>82260162</funding_grant_id><funding_grant_id>2022AB022</funding_grant_id><funding_grant_id>2023ZD037</funding_grant_id><funding_grant_id>62025102</funding_grant_id><funding_grant_id>2023AB057</funding_grant_id><funding_grant_id>82160156</funding_grant_id><funding_grant_id>2022ZD001</funding_grant_id><pubmed_authors>Xu L</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Chu X</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Hou Y</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Cui Q</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Yuan F</pubmed_authors><pubmed_authors>Zhao M</pubmed_authors><pubmed_authors>Xie J</pubmed_authors><pubmed_authors>Liang M</pubmed_authors><pubmed_authors>Su Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>KLF7 induced ADRB3-dependent IL-6 production in brown adipocytes during stress.</name><description>In recent studies, acute physiological stress has been shown to enhance liver gluconeogenesis by activating β3-adrenergic receptor (ADRB3)-dependent interleukin-6 (IL-6) production in brown adipocytes, effectively fueling "fight or flight" responses. However, the specific molecular mechanism of this IL-6 production in an ADRB3-dependent manner is not fully understood. ADRB3 regulates multiple metabolic programs in adipose tissue, including thermogenesis, lipolysis, and glucose uptake, by activating cAMP-PKA-CREB signaling. Our previous studies revealed that the transcription factor Krüppel-like factor 7 (KLF7) transcriptionally induces IL-6 expression in white adipocytes. Using Klf7-adipocyte knockout mice, we showed that Klf7 is also required for ADRB3-induced IL-6 production during stres</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-12T03:16:20.435Z</modification><creation>2026-07-12T03:08:03.535Z</creation></dates><accession>S-EPMC12925546</accession><cross_references><pubmed>41565113</pubmed><doi>10.1016/j.jlr.2026.100981</doi></cross_references></HashMap>