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dc.contributor.authorPuri, Vishwajeet
dc.contributor.authorCzech, Michael P.
dc.date2022-08-11T08:09:38.000
dc.date.accessioned2022-08-23T16:38:16Z
dc.date.available2022-08-23T16:38:16Z
dc.date.issued2008-07-26
dc.date.submitted2009-11-09
dc.identifier.citationJ Clin Invest. 2008 Aug;118(8):2693-6. <a href="http://dx.doi.org/10.1172/JCI36554">Link to article on publisher's site</a>
dc.identifier.issn0021-9738 (Print)
dc.identifier.doi10.1172/JCI36554
dc.identifier.pmid18654644
dc.identifier.urihttp://hdl.handle.net/20.500.14038/39208
dc.description.abstractFat-specific protein of 27 kDa (FSP27) is a highly expressed adipocyte protein that promotes triglyceride accumulation within lipid droplets. In this issue of the JCI, Nishino et al. show that FSP27 also helps to maintain the characteristically large unilocular lipid droplet structure within each white adipocyte (see the related article beginning on page 2808). Fragmentation of lipid droplets in white adipocytes from FSP27-KO mice caused both increased lipolysis and upregulation of genes enhancing mitochondrial oxidative metabolism. This increased energy expenditure in turn protected the mice from diet-induced obesity and insulin resistance. These new results highlight powerful mechanisms that tightly coordinate rates of triglyceride storage in lipid droplets with mitochondrial fatty acid oxidation in white adipocytes.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=18654644&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAdipocytes
dc.subjectAdipose Tissue, White
dc.subjectAnimals
dc.subjectCells, Cultured
dc.subjectEnergy Metabolism
dc.subjectFatty Acids, Nonesterified
dc.subjectLipolysis
dc.subjectMice
dc.subjectMice, Knockout
dc.subjectMitochondria
dc.subjectModels, Biological
dc.subjectOxidation-Reduction
dc.subjectProteins
dc.subjectUp-Regulation
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleLipid droplets: FSP27 knockout enhances their sizzle
dc.typeJournal Article
dc.source.journaltitleThe Journal of clinical investigation
dc.source.volume118
dc.source.issue8
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3013&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2014
dc.identifier.contextkey1058089
refterms.dateFOA2022-08-23T16:38:16Z
html.description.abstract<p>Fat-specific protein of 27 kDa (FSP27) is a highly expressed adipocyte protein that promotes triglyceride accumulation within lipid droplets. In this issue of the JCI, Nishino et al. show that FSP27 also helps to maintain the characteristically large unilocular lipid droplet structure within each white adipocyte (see the related article beginning on page 2808). Fragmentation of lipid droplets in white adipocytes from FSP27-KO mice caused both increased lipolysis and upregulation of genes enhancing mitochondrial oxidative metabolism. This increased energy expenditure in turn protected the mice from diet-induced obesity and insulin resistance. These new results highlight powerful mechanisms that tightly coordinate rates of triglyceride storage in lipid droplets with mitochondrial fatty acid oxidation in white adipocytes.</p>
dc.identifier.submissionpathoapubs/2014
dc.contributor.departmentProgram in Molecular Medicine
dc.source.pages2693-6


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