Characterization of Cre Recombinase Activity for In Vivo Targeting of Adipocyte Precursor Cells

被引:85
作者
Krueger, Katherine C. [1 ]
Costa, Maria Jose [1 ]
Du, Hongqing [1 ]
Feldman, Brian J. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Pediat Endocrinol, Stanford, CA 94305 USA
[2] Stanford Univ, Cardiovasc Inst, Stanford, CA 94305 USA
[3] Stanford Univ, Program Regenerat Med, Stanford, CA 94305 USA
来源
STEM CELL REPORTS | 2014年 / 3卷 / 06期
关键词
PROGENITOR CELLS; SUBCUTANEOUS FAT; ADIPOSE-TISSUE; STEM-CELLS; WHITE FAT; EXPRESSION; MICE; RECEPTOR; LINEAGE; MUSCLE;
D O I
10.1016/j.stemcr.2014.10.009
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The increased incidence of obesity and metabolic disease underscores the importance of elucidating the biology of adipose tissue development. The recent discovery of cell surface markers for prospective identification of adipose precursor cells (APCs) in vivo will greatly facilitate these studies, yet tools for specifically targeting these cells in vivo have not been identified. Here, we survey three transgenic mouse lines, Fabp4-Cre, PdgfR alpha-Cre, and Prx1-Cre, precisely assessing Cre-mediated recombination in adipose stromal populations and mature tissues. Our data provide key insights into the utility of these tools to modulate gene expression in adipose tissues. In particular, Fabp4-Cre is not effective to target APCs, nor is its activity restricted to these cells. PdgfRa-Cre directs recombination in the vast majority of APCs, but also targets other populations. In contrast, adipose expression of Prx1-Cre is chiefly limited to subcutaneous inguinal APCs, which will be valuable for dissection of APC functions among adipose depots.
引用
收藏
页码:1147 / 1158
页数:12
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