Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
The obesity-linked human lncRNA AATBC stimulates mitochondrial function in adipocytes.
EMBO Rep. 24:e57600 (2023)
Adipocytes are critical regulators of metabolism and energy balance. While white adipocyte dysfunction is a hallmark of obesity-associated disorders, thermogenic adipocytes are linked to cardiometabolic health. As adipocytes dynamically adapt to environmental cues by functionally switching between white and thermogenic phenotypes, a molecular understanding of this plasticity could help improving metabolism. Here, we show that the lncRNA Apoptosis associated transcript in bladder cancer (AATBC) is a human-specific regulator of adipocyte plasticity. Comparing transcriptional profiles of human adipose tissues and cultured adipocytes we discovered that AATBC was enriched in thermogenic conditions. Using primary and immortalized human adipocytes we found that AATBC enhanced the thermogenic phenotype, which was linked to increased respiration and a more fragmented mitochondrial network. Expression of AATBC in adipose tissue of mice led to lower plasma leptin levels. Interestingly, this association was also present in human subjects, as AATBC in adipose tissue was inversely correlated with plasma leptin levels, BMI, and other measures of metabolic health. In conclusion, AATBC is a novel obesity-linked regulator of adipocyte plasticity and mitochondrial function in humans.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Adipocyte ; Mitochondrial Dynamics ; Non-coding Rna ; Obesity ; Thermogenesis; Brown Adipose-tissue; Glucose-homeostasis; Rna-seq; Thermogenesis; Localization; Adaptation; Fission; Reveals; Brite; Ucp1
ISSN (print) / ISBN
1469-221X
e-ISSN
1469-3178
Zeitschrift
EMBO Reports
Quellenangaben
Band: 24,
Heft: 10,
Artikelnummer: e57600
Verlag
EMBO Press
Verlagsort
111 River St, Hoboken 07030-5774, Nj Usa
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Diabetes and Cancer (IDC)
Institute of Diabetes and Obesity (IDO)
Helmholtz Institute for Metabolism, Obesity and Vascular Research (HI-MAG)
Institute of Diabetes and Obesity (IDO)
Helmholtz Institute for Metabolism, Obesity and Vascular Research (HI-MAG)
Förderungen
EC | H2020 | PRIORITY 'Excellent science' | H2020 European Research Council (ERC)
Deutsches Zentrum für Herz-Kreislaufforschung (DZHK)
Deutsche Forschungsgemeinschaft (DFG)
Alexander von Humboldt-Stiftung (AvH)
Helmholtz Zentrum München (Helmholtz Centre Munich, German Research Center for Environmental Health)
Deutsches Zentrum für Herz-Kreislaufforschung (DZHK)
Deutsche Forschungsgemeinschaft (DFG)
Alexander von Humboldt-Stiftung (AvH)
Helmholtz Zentrum München (Helmholtz Centre Munich, German Research Center for Environmental Health)