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NR2B 包含的 NMDA 受体通过 CaMKIV/CREB 通路促进神经祖细胞增殖。

NR2B-containing NMDA receptors promote neural progenitor cell proliferation through CaMKIV/CREB pathway.

机构信息

Department of Anatomy and Neurobiology, Xuzhou Medical College, China.

出版信息

Biochem Biophys Res Commun. 2011 Aug 12;411(4):667-72. doi: 10.1016/j.bbrc.2011.06.170. Epub 2011 Jul 5.

Abstract

Accumulating evidence indicates the involvement of N-methyl-D-aspartate receptors (NMDARs) in regulating neural stem/progenitor cell (NSPC) proliferation. Functional properties of NMDARs can be markedly influenced by incorporating the regulatory subunit NR2B. Here, we aim to analyze the effect of NR2B-containing NMDARs on the proliferation of hippocampal NSPCs and to explore the mechanism responsible for this effect. NSPCs were shown to express NMDAR subunits NR1 and NR2B. The NR2B selective antagonist, Ro 25-6981, prevented the NMDA-induced increase in cell proliferation. Moreover, we demonstrated that the phosphorylation levels of calcium/calmodulin-dependent protein kinase IV (CaMKIV) and cAMP response element binding protein (CREB) were increased by NMDA treatment, whereas Ro 25-6981 decreased them. The role that NR2B-containing NMDARs plays in NSPC proliferation was abolished when CREB phosphorylation was attenuated by CaMKIV silencing. These results suggest that NR2B-containing NMDARs have a positive role in regulating NSPC proliferation, which may be mediated through CaMKIV phosphorylation and subsequent induction of CREB activation.

摘要

越来越多的证据表明 N-甲基-D-天冬氨酸受体(NMDARs)参与调节神经干细胞/祖细胞(NSPC)的增殖。NMDAR 的功能特性可以通过结合调节亚基 NR2B 而显著影响。在这里,我们旨在分析含有 NR2B 的 NMDAR 对海马 NSPC 增殖的影响,并探讨其作用机制。结果表明 NSPC 表达 NMDAR 亚基 NR1 和 NR2B。NR2B 选择性拮抗剂 Ro 25-6981 可阻止 NMDA 诱导的细胞增殖增加。此外,我们证明 NMDA 处理可增加钙/钙调蛋白依赖性蛋白激酶 IV(CaMKIV)和 cAMP 反应元件结合蛋白(CREB)的磷酸化水平,而 Ro 25-6981 则降低了它们的磷酸化水平。当通过 CaMKIV 沉默减弱 CREB 磷酸化时,NR2B 包含的 NMDAR 在 NSPC 增殖中的作用被消除。这些结果表明,NR2B 包含的 NMDAR 在调节 NSPC 增殖中具有积极作用,这可能是通过 CaMKIV 磷酸化和随后诱导 CREB 激活介导的。

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