<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tarale P</submitter><funding>NIAAA NIH HHS</funding><funding>NIAAA</funding><pagination>279</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11526652</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Microglia, a type of resident immune cells within the central nervous system, have been implicated in ethanol-activated neuronal death of the stress regulatory proopiomelanocortin (POMC) neuron-producing β-endorphin peptides in the hypothalamus in a postnatal rat model of fetal alcohol spectrum disorders. We determined if microglial extracellular vesicles (exosomes) are involved in the ethanol-induced neuronal death of the β-endorphin neuron via secreting elevated levels of the chemokine monocyte chemoattractant protein 1 (MCP1), a key regulator of neuroinflammation.&lt;h4>Methods&lt;/h4>We employed an in vitro model, consisting of primary culture of hypothalamic microglia prepared from postnatal day 2 (PND2) rat hypothalami and treated with or without 50 mM ethanol for 24 h, </pubmed_abstract><journal>Journal of neuroinflammation</journal><pubmed_title>Ethanol-activated microglial exosomes induce MCP1 signaling mediated death of stress-regulatory proopiomelanocortin neurons in the developing hypothalamus.</pubmed_title><pmcid>PMC11526652</pmcid><funding_grant_id>R01AA028767</funding_grant_id><funding_grant_id>R01 AA028767</funding_grant_id><pubmed_authors>Tarale P</pubmed_authors><pubmed_authors>Chaudhary S</pubmed_authors><pubmed_authors>Sarkar DK</pubmed_authors><pubmed_authors>Mukherjee S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ethanol-activated microglial exosomes induce MCP1 signaling mediated death of stress-regulatory proopiomelanocortin neurons in the developing hypothalamus.</name><description>&lt;h4>Background&lt;/h4>Microglia, a type of resident immune cells within the central nervous system, have been implicated in ethanol-activated neuronal death of the stress regulatory proopiomelanocortin (POMC) neuron-producing β-endorphin peptides in the hypothalamus in a postnatal rat model of fetal alcohol spectrum disorders. We determined if microglial extracellular vesicles (exosomes) are involved in the ethanol-induced neuronal death of the β-endorphin neuron via secreting elevated levels of the chemokine monocyte chemoattractant protein 1 (MCP1), a key regulator of neuroinflammation.&lt;h4>Methods&lt;/h4>We employed an in vitro model, consisting of primary culture of hypothalamic microglia prepared from postnatal day 2 (PND2) rat hypothalami and treated with or without 50 mM ethanol for 24 h, </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-05T09:12:28.228Z</modification><creation>2025-04-05T09:12:28.228Z</creation></dates><accession>S-EPMC11526652</accession><cross_references><pubmed>39478585</pubmed><doi>10.1186/s12974-024-03274-6</doi></cross_references></HashMap>