<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang Y</submitter><funding>Key Technologies Research and Development Program</funding><funding>Department of Science and Technology of Sichuan Province</funding><pagination>165</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8961928</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Browning of white adipose tissue (WAT) is a particularly appealing target for therapeutics in the treatment of obesity and related metabolic diseases. Although small extracellular vesicles (sEVs) released from adipose tissue (sEVs-AT) have emerged as novel player that regulate systemic metabolism by connecting different organs, the role of specific contents in sEVs-AT played in WAT browning has not been clarified.&lt;h4>Results&lt;/h4>We revealed Nucleophosmin3 (NPM3), which was mainly transferred by sEVs derived from brown adipose tissue (sEVs-BAT), was served as a batokine that could induce WAT browning by regulating the stability of PRDM16 mRNA. sEVs-BAT enhanced the expressions of browning related genes in 3T3-L1 preadipocytes and WAT while knocking down of NPM3 in BAT imp</pubmed_abstract><journal>Journal of nanobiotechnology</journal><pubmed_title>Nucleophosmin3 carried by small extracellular vesicles contribute to white adipose tissue browning.</pubmed_title><pmcid>PMC8961928</pmcid><funding_grant_id>2017YFA0104800</funding_grant_id><funding_grant_id>2019YFS0312</funding_grant_id><pubmed_authors>Yu M</pubmed_authors><pubmed_authors>Tian W</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Dong J</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nucleophosmin3 carried by small extracellular vesicles contribute to white adipose tissue browning.</name><description>&lt;h4>Background&lt;/h4>Browning of white adipose tissue (WAT) is a particularly appealing target for therapeutics in the treatment of obesity and related metabolic diseases. Although small extracellular vesicles (sEVs) released from adipose tissue (sEVs-AT) have emerged as novel player that regulate systemic metabolism by connecting different organs, the role of specific contents in sEVs-AT played in WAT browning has not been clarified.&lt;h4>Results&lt;/h4>We revealed Nucleophosmin3 (NPM3), which was mainly transferred by sEVs derived from brown adipose tissue (sEVs-BAT), was served as a batokine that could induce WAT browning by regulating the stability of PRDM16 mRNA. sEVs-BAT enhanced the expressions of browning related genes in 3T3-L1 preadipocytes and WAT while knocking down of NPM3 in BAT imp</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T19:10:21.918Z</modification><creation>2025-04-04T19:10:21.918Z</creation></dates><accession>S-EPMC8961928</accession><cross_references><pubmed>35346213</pubmed><doi>10.1186/s12951-022-01381-1</doi></cross_references></HashMap>