Zfp423 Expression Identifies Committed Preadipocytes and Localizes to Adipose Endothelial and Perivascular Cells

Progress has been made in elucidating the cell-surface phenotype of primary adipose progenitors; however, specific functional markers and distinct molecular signatures of fat depot-specific preadipocytes have remained elusive. In this study, we label committed murine adipose progenitors through expr...

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Veröffentlicht in:Cell metabolism 2012-02, Vol.15 (2), p.230-239
Hauptverfasser: Gupta, Rana K., Mepani, Rina J., Kleiner, Sandra, Lo, James C., Khandekar, Melin J., Cohen, Paul, Frontini, Andrea, Bhowmick, Diti Chatterjee, Ye, Li, Cinti, Saverio, Spiegelman, Bruce M.
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Sprache:eng
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Zusammenfassung:Progress has been made in elucidating the cell-surface phenotype of primary adipose progenitors; however, specific functional markers and distinct molecular signatures of fat depot-specific preadipocytes have remained elusive. In this study, we label committed murine adipose progenitors through expression of GFP from the genetic locus for Zfp423, a gene controlling preadipocyte determination. Selection of GFP-expressing fibroblasts from either subcutaneous or visceral adipose-derived stromal vascular cultures isolates stably committed preadipocytes that undergo robust adipogenesis. Immunohistochemistry for Zfp423-driven GFP expression in vivo confirms a perivascular origin of preadipocytes within both white and brown adipose tissues. Interestingly, a small subset of capillary endothelial cells within white and brown fat also express this marker, suggesting a contribution of specialized endothelial cells to the adipose lineage. Zfp423GFP mice represent a simple tool for the specific localization and isolation of molecularly defined preadipocytes from distinct adipose tissue depots. ► Adipose progenitors are labeled through expression of GFP from the locus for Zfp423 ► GFP+ fibroblasts from adipose stromal vascular cultures undergo adipogenesis ► Zfp423-driven GFP expression localizes to perivascular cells of WAT and BAT ► A subset of capillary endothelial cells within WAT and BAT also express this marker
ISSN:1550-4131
1932-7420
DOI:10.1016/j.cmet.2012.01.010