کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2035999 1072240 2012 11 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوشیمی، ژنتیک و زیست شناسی مولکولی (عمومی)
پیش نمایش صفحه اول مقاله
Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human
چکیده انگلیسی

SummaryBrown fat generates heat via the mitochondrial uncoupling protein UCP1, defending against hypothermia and obesity. Recent data suggest that there are two distinct types of brown fat: classical brown fat derived from a myf-5 cellular lineage and UCP1-positive cells that emerge in white fat from a non-myf-5 lineage. Here, we report the isolation of “beige” cells from murine white fat depots. Beige cells resemble white fat cells in having extremely low basal expression of UCP1, but, like classical brown fat, they respond to cyclic AMP stimulation with high UCP1 expression and respiration rates. Beige cells have a gene expression pattern distinct from either white or brown fat and are preferentially sensitive to the polypeptide hormone irisin. Finally, we provide evidence that previously identified brown fat deposits in adult humans are composed of beige adipocytes. These data provide a foundation for studying this mammalian cell type with therapeutic potential.PaperClip To listen to this audio, enable JavaScript on your browser. However, you can download and play the audio by clicking on the icon belowHelp with MP3 filesOptionsDownload audio (3198 K)

Graphical AbstractFigure optionsDownload high-quality image (234 K)Download as PowerPoint slideHighlights
► A subset of precursor cells from white fat gives rise to beige adipocytes
► Beige adipocytes have a highly inducible thermogenic capacity upon stimulation
► Beige adipocytes express distinct genes and are sensitive to irisin
► “Brown” fat in human adults is composed primarily of beige adipocytes

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: - Volume 150, Issue 2, 20 July 2012, Pages 366–376
نویسندگان
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