Excitatory amino acid transporter 1 supports adult hippocampal neural stem cell self-renewal

被引:5
|
作者
Rieskamp, Joshua D. [1 ,6 ]
Rosado-Burgos, Ileanexis [1 ]
Christofi, Jacob E. [1 ]
Ansar, Eliza [1 ,5 ]
Einstein, Dalia [1 ]
Walters, Ashley E. [1 ]
Valentini, Valentina [1 ,4 ]
Bruno, John P. [1 ,2 ]
Kirby, Elizabeth D. [1 ,2 ,3 ]
机构
[1] Ohio State Univ, Dept Psychol, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Neurosci, Columbus, OH 43210 USA
[3] Ohio State Univ, Chron Brain Injury Program, Columbus, OH 43210 USA
[4] Univ Cagliari, Dept Biomed Sci, I-09124 Cagliari, Italy
[5] New York Coll Podiatr Med, New York, NY 10035 USA
[6] Global Regulatory Writing & Consulting, Tukwila, WA 98168 USA
基金
美国国家卫生研究院;
关键词
PROGENITOR CELLS; DENTATE GYRUS; RADIAL GLIA; NEUROGENESIS; GLUTAMATE; LONG; QUIESCENCE; ASTROCYTES; RECEPTORS; CYTOSCAPE;
D O I
10.1016/j.isci.2023.107068
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Within the adult mammalian dentate gyrus (DG) of the hippocampus, glutamate stimulates neural stem cell (NSC) self-renewing proliferation, providing a link between adult neurogenesis and local circuit activity. Here, we show that glutamate-induced self-renewal of adult DG NSCs requires glutamate transport via excitatory amino acid transporter 1 (EAAT1) to stimulate lipogenesis. Loss of EAAT1 prevented glutamate-induced self-renewing proliferation of NSCs in vitro and in vivo, with little role evident for canonical glutamate receptors. Transcriptomics and further pathway manipulation revealed that glutamate simulation of NSCs relied on EAAT1 transport-stimulated lipogenesis. Our findings demonstrate a critical, direct role for EAAT1 in stimulating NSCs to support neurogenesis in adulthood, thereby providing insights into a non-canonical mechanism by which NSCs sense and respond to their niche.
引用
收藏
页数:25
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