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.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-10-01 Epub Date: 2024-01-05 DOI:10.1007/s12011-023-04033-z
Hideki Mori, Akari Goji, Masayuki Hara
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引用次数: 0

Abstract

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 μM 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 μM 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.

体外神经干/祖细胞分化后细胞内锌离子水平的上调与锌转运体基因表达的变化
我们测量了小鼠胎儿神经干/祖细胞(NSPCs)和分化细胞的胞内锌离子浓度。用 1.5 μM Zn2+培养的神经干/祖细胞的增殖速度略快于缺锌培养基,用 1.5 μM Zn2+培养的神经干/祖细胞及其分化细胞(DC)的胞内锌浓度分别比缺锌培养基高 1.34 倍和 2.00 倍。在NSPCs向DCs分化的过程中,锌转运体基因上调超过3.5倍的有Zip1、Zip4、Zip12、Zip13、ZnT1、ZnT8和ZnT10,而下调的只有Zip8。在2%O2和5%CO2的低氧培养条件、21%O2和10%CO2的高二氧化碳培养条件以及21%O2和5%CO2的正常培养条件下,NSPCs和DCs的细胞形态基本相同。Zip4、Zip8、Zip12和Zip14的表达并没有因为氧气和二氧化碳浓度的不同而发生很大变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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