Upregulation of Intracellular Zinc Ion Level after Differentiation of the Neural Stem/Progenitor Cells In Vitro with the Changes in Gene Expression of Zinc Transporters

被引:1
作者
Mori, Hideki [1 ]
Goji, Akari [1 ]
Hara, Masayuki [1 ]
机构
[1] Osaka Metropolitan Univ, Grad Sch Sci, Dept Biol Chem, 1-1 Gakuencho,Nakaku, Sakai, Osaka 5998531, Japan
基金
日本学术振兴会;
关键词
Zinc; ZnT; ZIP; Neural stem cell; Transporter; Differentiation; TRANSCRIPTION FACTOR-I; STEM-CELLS; NEUROGENESIS; ROLES; NEURONS; ZIP8; ZRT;
D O I
10.1007/s12011-023-04033-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We measured the intracellular zinc ion concentration of murine fetal neural stem/progenitor cells (NSPCs) and that in the differentiated cells. The NSPCs cultured with 1.5 mu M Zn2+ proliferated slightly faster than that in the zinc-deficient medium and the intracellular zinc concentration of the NSPCs and that of their differentiated cells (DCs) cultured with 1.5 mu M Zn2+ was 1.34-fold and 2.00-fold higher than those in the zinc-deficient medium, respectively. The zinc transporter genes upregulated over the 3.5-fold change were Zip1, Zip4, Zip12, Zip13, ZnT1, ZnT8, and ZnT10 whereas the only downregulated one was Zip8 during the differentiation of NSPCs to DCs. The cell morphologies of both NSPCs and DCs in the low oxygen culture condition consisting of 2%O2 and 5%CO2, the high carbon dioxide condition consisting of 21%O2 and 10%CO2, and the normal condition consisting of 21%O2 and 5%CO2 were essentially the same each other. The expression of Zip4, Zip8, Zip12, and Zip14 was not drastically changed depending on the O2 and CO2 concentrations.
引用
收藏
页码:4699 / 4714
页数:16
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