کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5559833 | 1561691 | 2017 | 8 صفحه PDF | دانلود رایگان |
- Types of expressed ZIP gene changed during differentiation of NSPCs.
- Expression of Zip8 was downregulated after differentiation of NSPCs.
- Expression of Zip4 and Zip12 was upregulated after differentiation of NSPCs.
- ZIP8 was detected in cultured NSPCs and subventricular zone of embryonic brain.
Zinc plays important roles for brain development. Zrt-, Irt-related protein (ZIP) is a major transporter family to regulate the intracellular zinc levels. Neural stem/progenitor cells (NSPCs) are more sensitive than their differentiated progeny (neural/glial cells) to zinc in vitro (Nishikawa et al., 2015). We analyzed relative gene expression of 14 different ZIPs in murine NSPCs and differentiated cells by real-time polymerase chain reaction technique. Expression of Zip4 and that of Zip12 drastically increased, while that of Zip8 clearly decreased after differentiation of NSPCs. Downregulation of NSPC's marker (Nes) and upregulation of differentiated cell markers (Tubb3; neuron, Gfap; astrocyte) occurred simultaneously. ZIP8 protein was immunochemically detected both in cultured neurospheres consisting of NSPCs in vitro and in subventricular zone of embryonic mouse brain in vivo, like a novel surface marker of NSPCs. We considered that required types of ZIP changed during the differetiation of NSPCs.
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Journal: Environmental Toxicology and Pharmacology - Volume 53, July 2017, Pages 81-88