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miR-155 regulates differentiation of brown and beige adipocytes via a bistable circuit

dc.contributor.advisorPfeifer, Alexander
dc.contributor.authorChen, Yong
dc.date.accessioned2020-04-19T23:26:24Z
dc.date.available2020-04-19T23:26:24Z
dc.date.issued03.07.2014
dc.identifier.urihttps://hdl.handle.net/20.500.11811/6116
dc.description.abstractBrown adipocytes are a primary site of energy expenditure and reside not only in classical brown adipose tissue but can also be found in white adipose tissue. Here we show that microRNA 155 is enriched in brown adipose tissue and is highly expressed in proliferating brown preadipocytes but declines after induction of differentiation. Interestingly, microRNA 155 and its target, the adipogenic transcription factor CCAAT/enhancer-binding protein b, form a bistable feedback loop integrating hormonal signals that regulate proliferation or differentiation. Inhibition of microRNA 155 enhances brown adipocyte differentiation and induces a brown adipocyte-like phenotype (‘browning’) in white adipocytes. Consequently, microRNA 155- deficient mice exhibit increased brown adipose tissue function and ‘browning’ of white fat tissue. In contrast, transgenic overexpression of microRNA 155 in mice causes a reduction of brown adipose tissue mass and impairment of brown adipose tissue function. These data demonstrate that the bistable loop involving microRNA 155 and CCAAT/enhancer-binding protein b regulates brown lineage commitment, thereby, controlling the development of brown and beige fat cells.en
dc.language.isoeng
dc.rightsIn Copyright
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectmiRNA
dc.subjectbrown adipose tissue
dc.subjectdifferentiation
dc.subject.ddc500 Naturwissenschaften
dc.titlemiR-155 regulates differentiation of brown and beige adipocytes via a bistable circuit
dc.typeDissertation oder Habilitation
dc.publisher.nameUniversitäts- und Landesbibliothek Bonn
dc.publisher.locationBonn
dc.rights.accessRightsopenAccess
dc.identifier.urnhttps://nbn-resolving.org/urn:nbn:de:hbz:5n-36587
ulbbn.pubtypeErstveröffentlichung
ulbbnediss.affiliation.nameRheinische Friedrich-Wilhelms-Universität Bonn
ulbbnediss.affiliation.locationBonn
ulbbnediss.thesis.levelDissertation
ulbbnediss.dissID3658
ulbbnediss.date.accepted18.06.2014
ulbbnediss.instituteMedizinische Fakultät / Institute : Institut für Pharmakologie und Toxikologie
ulbbnediss.fakultaetMathematisch-Naturwissenschaftliche Fakultät
dc.contributor.coRefereeFürst, Dieter O.


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