<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guo X</submitter><funding>U.S. Department of Health and Human Services</funding><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><pagination>114192</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11197849</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(5)</volume><pubmed_abstract>The preoptic area of the hypothalamus (POA) is essential for sleep regulation. However, the cellular makeup of the POA is heterogeneous, and the molecular identities of the sleep-promoting cells remain elusive. To address this question, this study compares mice during recovery sleep following sleep deprivation to mice allowed extended sleep. Single-nucleus RNA sequencing (single-nucleus RNA-seq) identifies one galanin inhibitory neuronal subtype that shows upregulation of rapid and delayed activity-regulated genes during recovery sleep. This cell type expresses higher levels of growth hormone receptor and lower levels of estrogen receptor compared to other galanin subtypes. single-nucleus RNA-seq also reveals cell-type-specific upregulation of purinergic receptor (P2ry14) and serotonin rec</pubmed_abstract><journal>Cell reports</journal><pubmed_title>Single-nucleus RNA-seq identifies one galanin neuronal subtype in mouse preoptic hypothalamus activated during recovery from sleep deprivation.</pubmed_title><pmcid>PMC11197849</pmcid><funding_grant_id>R21NS122370</funding_grant_id><funding_grant_id>R21 NS122370</funding_grant_id><pubmed_authors>Lian J</pubmed_authors><pubmed_authors>Pack AI</pubmed_authors><pubmed_authors>Keenan BT</pubmed_authors><pubmed_authors>Reiner BC</pubmed_authors><pubmed_authors>Guo X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-nucleus RNA-seq identifies one galanin neuronal subtype in mouse preoptic hypothalamus activated during recovery from sleep deprivation.</name><description>The preoptic area of the hypothalamus (POA) is essential for sleep regulation. However, the cellular makeup of the POA is heterogeneous, and the molecular identities of the sleep-promoting cells remain elusive. To address this question, this study compares mice during recovery sleep following sleep deprivation to mice allowed extended sleep. Single-nucleus RNA sequencing (single-nucleus RNA-seq) identifies one galanin inhibitory neuronal subtype that shows upregulation of rapid and delayed activity-regulated genes during recovery sleep. This cell type expresses higher levels of growth hormone receptor and lower levels of estrogen receptor compared to other galanin subtypes. single-nucleus RNA-seq also reveals cell-type-specific upregulation of purinergic receptor (P2ry14) and serotonin rec</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2025-04-20T02:15:06.729Z</modification><creation>2025-04-20T02:15:06.729Z</creation></dates><accession>S-EPMC11197849</accession><cross_references><pubmed>38703367</pubmed><doi>10.1016/j.celrep.2024.114192</doi></cross_references></HashMap>