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Myogenic gene expression signature establishes that brown and white adipocytes originate from distinct cell lineages.

Timmons, James A (författare)
Wennmalm, Kristian (författare)
Karolinska Institutet
Larsson, Ola (författare)
Karolinska Institutet
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Walden, Tomas B (författare)
Stockholms universitet,Wenner-Grens institut
Lassmann, Timo (författare)
Petrovic, Natasa (författare)
Stockholms universitet,Wenner-Grens institut
Hamilton, D Lee (författare)
Gimeno, Ruth E (författare)
Wahlestedt, Claes (författare)
Baar, Keith (författare)
Nedergaard, Jan (författare)
Stockholms universitet,Wenner-Grens institut
Cannon, Barbara (författare)
Stockholms universitet,Wenner-Grens institut
visa färre...
 (creator_code:org_t)
2007-03-13
2007
Engelska.
Ingår i: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 104:11, s. 4401-4406
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Attainment of a brown adipocyte cell phenotype in white adipocytes, with their abundant mitochondria and increased energy expenditure potential, is a legitimate strategy for combating obesity. The unique transcriptional regulators of the primary brown adipocyte phenotype are unknown, limiting our ability to promote brown adipogenesis over white. In the present work, we used microarray analysis strategies to study primary preadipocytes, and we made the striking discovery that brown preadipocytes demonstrate a myogenic transcriptional signature, whereas both brown and white primary preadipocytes demonstrate signatures distinct from those found in immortalized adipogenic models. We found a plausible SIRT1-related transcriptional signature during brown adipocyte differentiation that may contribute to silencing the myogenic signature. In contrast to brown preadipocytes or skeletal muscle cells, white preadipocytes express Tcf21, a transcription factor that has been shown to suppress myogenesis and nuclear receptor activity. In addition, we identified a number of developmental genes that are differentially expressed between brown and white preadipocytes and that have recently been implicated in human obesity. The interlinkage between the myocyte and the brown preadipocyte confirms the distinct origin for brown versus white adipose tissue and also represents a plausible explanation as to why brown adipocytes ultimately specialize in lipid catabolism rather than storage, much like oxidative skeletal muscle tissue.

Nyckelord

Adipocytes/*cytology
Adipose Tissue; Brown/*cytology
Animals
Basic Helix-Loop-Helix Transcription Factors/metabolism
Cell Differentiation
Cell Lineage
Gene Expression Regulation
Gene Silencing
Lipids/chemistry
Male
Mice
Muscle; Skeletal/*cytology/metabolism
Oxygen/metabolism
Principal Component Analysis
Sirtuins/metabolism

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