Prepubertal androgen signaling is required to establish male fat distribution

被引:6
作者
Sebo, Zachary L. [1 ,2 ,5 ]
Rodeheffer, Matthew S. [2 ,3 ,4 ,5 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Dept Comparat Med, Sch Med, 375 Congress Ave, New Haven, CT 06520 USA
[3] Yale Univ, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
[4] Yale Univ, Yale Stem Cell Ctr, New Haven, CT 06520 USA
[5] Yale Univ, Yale Program Integrat Cell Signaling & Neurobiol, New Haven, CT 06520 USA
基金
美国国家科学基金会;
关键词
ADIPOSE-TISSUE DEVELOPMENT; BODY-FAT; ADIPONECTIN; ADIPOGENESIS; CELLULARITY; GROWTH; ONSET; GENE;
D O I
10.1016/j.stemcr.2022.04.001
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Fat distribution is sexually dimorphic and is associated with metabolic disease risk. It is unknown if prepubertal sex-hormone signaling influences adult fat distribution. Here, we show that karyotypically male androgen-insensitive mice exhibit pronounced subcutaneous adiposity compared with wild-type males and females. This subcutaneous adipose bias emerges prior to puberty and is not due to differences in adipocyte size or rates of adipogenesis between visceral and subcutaneous fat. Instead, we find that androgen-insensitive mice lack an adequate progenitor pool for normal visceral-fat expansion during development, thus increasing the subcutaneous-to-visceral-fat ratio. Obesogenic visceral-fat expansion is likewise inhibited in these mice, yet their metabolic health is similar to wild-type animals with comparable total fat mass. Taken together, these data show that adult fat distribution can be determined prior to the onset of puberty by the relative number of progenitors that seed nascent adipose depots.
引用
收藏
页码:1081 / 1088
页数:8
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