<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Luk C</submitter><funding>British Heart Foundation</funding><funding>Medical Research Council</funding><funding>Diabetes UK</funding><funding>Wellcome Trust</funding><funding>Biotechnology and Biological Sciences Research Council</funding><pagination>170</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11696296</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>During recent decades, changes in lifestyle have led to widespread nutritional obesity and its related complications. Remodelling adipose tissue as a therapeutic goal for obesity and its complications has attracted much attention and continues to be actively explored. The endothelium lines all blood vessels and is close to all cells, including adipocytes. The endothelium has been suggested to act as a paracrine organ. We explore the role of endothelial insulin-like growth factor-1 receptor (IGF-1R), as a paracrine modulator of white adipose phenotype. We show that a reduction in endothelial IGF-1R expression in the presence of high-fat feeding in male mice leads to depot-specific beneficial white adipose tissue remodelling, increases whole-body energy expenditure and enhances insulin sensi</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Paracrine role of endothelial IGF-1 receptor in depot-specific adipose tissue adaptation in male mice.</pubmed_title><pmcid>PMC11696296</pmcid><funding_grant_id>FS/19/59/34896</funding_grant_id><funding_grant_id>BB/R013500/1</funding_grant_id><funding_grant_id>PG/14/54/30939</funding_grant_id><funding_grant_id>110158/Z/15/Z</funding_grant_id><funding_grant_id>MR/X009734/1</funding_grant_id><funding_grant_id>RG/15/7/31521</funding_grant_id><funding_grant_id>PG/18/82/34120</funding_grant_id><funding_grant_id>16/0005382</funding_grant_id><funding_grant_id>220257/Z/20/Z</funding_grant_id><funding_grant_id>FS/12/80/29821</funding_grant_id><funding_grant_id>FS/19/59/34896A</funding_grant_id><pubmed_authors>Vidal-Puig A</pubmed_authors><pubmed_authors>Bruns AF</pubmed_authors><pubmed_authors>Kearney MT</pubmed_authors><pubmed_authors>Griffin KJ</pubmed_authors><pubmed_authors>Sukumar P</pubmed_authors><pubmed_authors>MacCannell ADV</pubmed_authors><pubmed_authors>Hartley RC</pubmed_authors><pubmed_authors>Simon Futers T</pubmed_authors><pubmed_authors>Warmke N</pubmed_authors><pubmed_authors>Prag HA</pubmed_authors><pubmed_authors>Ozber CH</pubmed_authors><pubmed_authors>Limumpornpetch S</pubmed_authors><pubmed_authors>Wheatcroft SB</pubmed_authors><pubmed_authors>Simmons KJ</pubmed_authors><pubmed_authors>Yuldasheva NY</pubmed_authors><pubmed_authors>Brown OI</pubmed_authors><pubmed_authors>Murphy MP</pubmed_authors><pubmed_authors>Witte KK</pubmed_authors><pubmed_authors>Mughal R</pubmed_authors><pubmed_authors>Drozd M</pubmed_authors><pubmed_authors>Skromna A</pubmed_authors><pubmed_authors>Wilkinson CG</pubmed_authors><pubmed_authors>Luk C</pubmed_authors><pubmed_authors>Watt NT</pubmed_authors><pubmed_authors>Beech DJ</pubmed_authors><pubmed_authors>Bridge KI</pubmed_authors><pubmed_authors>Moran A</pubmed_authors><pubmed_authors>Viswambharan H</pubmed_authors><pubmed_authors>Scragg JL</pubmed_authors><pubmed_authors>Smith J</pubmed_authors><pubmed_authors>Straw S</pubmed_authors><pubmed_authors>Haywood NJ</pubmed_authors><pubmed_authors>Cubbon RM</pubmed_authors><pubmed_authors>Cheng CW</pubmed_authors><pubmed_authors>Makava N</pubmed_authors><pubmed_authors>Walker AM</pubmed_authors><pubmed_authors>Roberts LD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Paracrine role of endothelial IGF-1 receptor in depot-specific adipose tissue adaptation in male mice.</name><description>During recent decades, changes in lifestyle have led to widespread nutritional obesity and its related complications. Remodelling adipose tissue as a therapeutic goal for obesity and its complications has attracted much attention and continues to be actively explored. The endothelium lines all blood vessels and is close to all cells, including adipocytes. The endothelium has been suggested to act as a paracrine organ. We explore the role of endothelial insulin-like growth factor-1 receptor (IGF-1R), as a paracrine modulator of white adipose phenotype. We show that a reduction in endothelial IGF-1R expression in the presence of high-fat feeding in male mice leads to depot-specific beneficial white adipose tissue remodelling, increases whole-body energy expenditure and enhances insulin sensi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-06-02T02:05:07.734Z</modification><creation>2025-04-05T22:52:55.091Z</creation></dates><accession>S-EPMC11696296</accession><cross_references><pubmed>39747815</pubmed><doi>10.1038/s41467-024-54669-1</doi></cross_references></HashMap>