38
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      A classical brown adipose tissue mRNA signature partly overlaps with brite in the supraclavicular region of adult humans.

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Human brown adipose tissue (BAT) has been detected in adults but was recently suggested to be of brite/beige origin. We collected BAT from the supraclavicular region in 21 patients undergoing surgery for suspected cancer in the neck area and assessed the gene expression of established murine markers for brown, brite/beige, and white adipocytes. We demonstrate that a classical brown expression signature, including upregulation of miR-206, miR-133b, LHX8, and ZIC1 and downregulation of HOXC8 and HOXC9, coexists with an upregulation of two newly established brite/beige markers, TBX1 and TMEM26. A similar mRNA expression profile was observed when comparing isolated human adipocytes from BAT and white adipose tissue (WAT) depots, differentiated in vitro. In conclusion, our data suggest that human BAT might consist of both classical brown and recruitable brite adipocytes, an observation important for future considerations on how to induce human BAT.

          Related collections

          Author and article information

          Journal
          Cell Metab
          Cell metabolism
          Elsevier BV
          1932-7420
          1550-4131
          May 07 2013
          : 17
          : 5
          Affiliations
          [1 ] Centre of Inflammation and Metabolism, Department of Infectious Diseases, Rigshospitalet, DK-2100 Copenhagen, Denmark.
          Article
          S1550-4131(13)00154-X
          10.1016/j.cmet.2013.04.011
          23663743
          ab88c633-a459-45aa-aab4-05fd86252160
          Copyright © 2013 Elsevier Inc. All rights reserved.
          History

          Comments

          Comment on this article