<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Holman CD</submitter><funding>NICHD NIH HHS</funding><funding>NIDDK NIH HHS</funding><pubmed_abstract>The energy-burning capability of beige adipose tissue is a potential therapeutic tool for reducing obesity and metabolic disease, but this capacity is decreased by aging. Here, we evaluate the impact of aging on the profile and activity of adipocyte stem and progenitor cells (ASPCs) and adipocytes during the beiging process. We found that aging increases the expression of &lt;i>Cd9&lt;/i> and other fibro-inflammatory genes in fibroblastic ASPCs and blocks their differentiation into beige adipocytes. Fibroblastic ASPC populations from young and aged mice were equally competent for beige differentiation &lt;i>in vitro&lt;/i>, suggesting that environmental factors suppress adipogenesis &lt;i>in vivo&lt;/i>. Examination of adipocytes by single nucleus RNA-sequencing identified compositional and transcriptional </pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2023.03.20.533514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10055201</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aging impairs cold-induced beige adipogenesis and adipocyte metabolic reprogramming.</pubmed_title><pmcid>PMC10055201</pmcid><funding_grant_id>R01 DK121801</funding_grant_id><funding_grant_id>P30 DK046200</funding_grant_id><funding_grant_id>P30 DK019525</funding_grant_id><funding_grant_id>R01 DK120982</funding_grant_id><funding_grant_id>P30 DK135043</funding_grant_id><funding_grant_id>R01 DK123356</funding_grant_id><funding_grant_id>RC2 DK116691</funding_grant_id><funding_grant_id>P30 DK057521</funding_grant_id><funding_grant_id>T32 DK007314</funding_grant_id><funding_grant_id>T32 HD083185</funding_grant_id><pubmed_authors>Holman CD</pubmed_authors><pubmed_authors>Seale P</pubmed_authors><pubmed_authors>Rosen ED</pubmed_authors><pubmed_authors>Sakers AP</pubmed_authors><pubmed_authors>Cheng L</pubmed_authors><pubmed_authors>Calhoun RP</pubmed_authors><pubmed_authors>Jacobs C</pubmed_authors><pubmed_authors>Tsai L</pubmed_authors><pubmed_authors>Fein EC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aging impairs cold-induced beige adipogenesis and adipocyte metabolic reprogramming.</name><description>The energy-burning capability of beige adipose tissue is a potential therapeutic tool for reducing obesity and metabolic disease, but this capacity is decreased by aging. Here, we evaluate the impact of aging on the profile and activity of adipocyte stem and progenitor cells (ASPCs) and adipocytes during the beiging process. We found that aging increases the expression of &lt;i>Cd9&lt;/i> and other fibro-inflammatory genes in fibroblastic ASPCs and blocks their differentiation into beige adipocytes. Fibroblastic ASPC populations from young and aged mice were equally competent for beige differentiation &lt;i>in vitro&lt;/i>, suggesting that environmental factors suppress adipogenesis &lt;i>in vivo&lt;/i>. Examination of adipocytes by single nucleus RNA-sequencing identified compositional and transcriptional </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-07-06T03:15:27.148Z</modification><creation>2026-07-06T03:08:41.829Z</creation></dates><accession>S-EPMC10055201</accession><cross_references><pubmed>36993336</pubmed><doi>10.1101/2023.03.20.533514</doi></cross_references></HashMap>