Rodeheffer Matthew S, Birsoy Kivanç, Friedman Jeffrey M
Laboratory of Molecular Genetics, The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
Cell. 2008 Oct 17;135(2):240-9. doi: 10.1016/j.cell.2008.09.036. Epub 2008 Oct 2.
The increased white adipose tissue (WAT) mass associated with obesity is the result of both hyperplasia and hypertrophy of adipocytes. However, the mechanisms controlling adipocyte number are unknown in part because the identity of the physiological adipocyte progenitor cells has not been defined in vivo. In this report, we employ a variety of approaches, including a noninvasive assay for following fat mass reconstitution in vivo, to identify a subpopulation of early adipocyte progenitor cells (Lin(-):CD29(+):CD34(+):Sca-1(+):CD24(+)) resident in adult WAT. When injected into the residual fat pads of A-Zip lipodystrophic mice, these cells reconstitute a normal WAT depot and rescue the diabetic phenotype that develops in these animals. This report provides the identification of an undifferentiated adipocyte precursor subpopulation resident within the adipose tissue stroma that is capable of proliferating and differentiating into an adipose depot in vivo.
与肥胖相关的白色脂肪组织(WAT)量增加是脂肪细胞增生和肥大的结果。然而,控制脂肪细胞数量的机制尚不清楚,部分原因是生理脂肪细胞祖细胞的身份在体内尚未明确。在本报告中,我们采用了多种方法,包括一种用于在体内跟踪脂肪量重建的非侵入性检测方法,以鉴定成年WAT中存在的早期脂肪细胞祖细胞亚群(Lin(-):CD29(+):CD34(+):Sca-1(+):CD24(+))。当将这些细胞注射到A-Zip脂肪营养不良小鼠的残余脂肪垫中时,它们可重建正常的WAT库,并挽救这些动物中出现的糖尿病表型。本报告鉴定出了一种存在于脂肪组织基质中的未分化脂肪细胞前体亚群,该亚群能够在体内增殖并分化为一个脂肪库。