Adipocyte amino acid sensing controls adult germline stem cell number via the amino acid response pathway and independently of Target of Rapamycin signaling in Drosophila

被引:53
作者
Armstrong, Alissa R. [1 ,2 ]
Laws, Kaitlin M. [1 ,2 ]
Drummond-Barbosa, Daniela [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biochem & Mol Biol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Div Reprod Biol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA
来源
DEVELOPMENT | 2014年 / 141卷 / 23期
基金
美国国家卫生研究院;
关键词
Germline stem cells; Adipocytes; Amino acid transporters; Diet; Oogenesis; Drosophila; FAT-BODY; INSULIN; GROWTH; OBESITY; HOMEOSTASIS; METABOLISM; DIVISION; ECDYSONE; NICHE; DIET;
D O I
10.1242/dev.116467
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
How adipocytes contribute to the physiological control of stem cells is a critical question towards understanding the link between obesity and multiple diseases, including cancers. Previous studies have revealed that adult stem cells are influenced by whole-body physiology through multiple diet-dependent factors. For example, nutrient-dependent pathways acting within the Drosophila ovary control the number and proliferation of germline stem cells (GSCs). The potential role of nutrient sensing by adipocytes in modulating stem cells in other organs, however, remains largely unexplored. Here, we report that amino acid sensing by adult adipocytes specifically modulates the maintenance of GSCs through a Target of Rapamycin-independent mechanism. Instead, reduced amino acid levels and the consequent increase in uncoupled tRNAs trigger activation of the GCN2-dependent amino acid response pathway within adipocytes, causing increased rates of GSC loss. These studies reveal a new step in adipocyte-stem cell crosstalk.
引用
收藏
页码:4479 / 4488
页数:10
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