4.7 Article

Brown adipocytes can display a mammary basal myoepithelial cell phenotype in vivo

期刊

MOLECULAR METABOLISM
卷 6, 期 10, 页码 1198-1211

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molmet.2017.07.015

关键词

Brown adipocytes; Mammary gland; Lactation; Basal myoepithelial cells; Beige/brite adipocytes

资金

  1. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB13030000]
  2. CAS-Novonordisk Foundation

向作者/读者索取更多资源

Objective: Previous work has suggested that white adipocytes may also show a mammary lumina! secretory cell phenotype during lactation, The capacity of brown and beige/brite adipocytes to display a mammary cell phenotype and the levels at which they demonstrate such phenotypes in vivo is currently unknown. Methods: To investigate the putative adipocyte origin of mammary gland cells, we performed genetic lineage-labeling experiments in BAT and the mammary glands. Results: These studies indicated that the classic brown adipocytes (Ucp1(+)) and subcutaneous beige/brite adipocytes (Ucp1(-/+)) were found in the mammary gland during lactation, when they exhibited a mammary myoepithelial phenotype. Up to 2.5% of the anterior dorsal interscapular mammary myoepithelial cell population had a brown adipocyte origin with an adipose and myoepithelial gene signature during lactation. Eliminating these cells, along with all the brown adipocytes, significantly slowed offspring growth, potentially demonstrating their functional importance. Additionally, we showed mammary epithelial lineage Mmtv(+) and Krt14(+) cells expressed brown adipocyte markers after weaning, demonstrating that mammary gland cells can display an adipose phenotype. Conclusions: The identification of a brown adipocyte origin of mammary myoepithelial cells provides a novel perspective on the interrelationships between adipocytes and mammary cells with implications for our understanding of obesity and breast cancer. (C) 2017 The Authors, Published by Elsevier GmbH.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据