pubmed-article:21762679 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C0038250 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C0599851 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C0596290 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C1150537 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C0056695 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C0080093 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C0033414 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C1704259 | lld:lifeskim |
pubmed-article:21762679 | lifeskim:mentions | umls-concept:C1705987 | lld:lifeskim |
pubmed-article:21762679 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:21762679 | pubmed:dateCreated | 2011-8-15 | lld:pubmed |
pubmed-article:21762679 | pubmed:abstractText | 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. | lld:pubmed |
pubmed-article:21762679 | pubmed:language | eng | lld:pubmed |
pubmed-article:21762679 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21762679 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:21762679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21762679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21762679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21762679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21762679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21762679 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21762679 | pubmed:month | Aug | lld:pubmed |
pubmed-article:21762679 | pubmed:issn | 1090-2104 | lld:pubmed |
pubmed-article:21762679 | pubmed:author | pubmed-author:JulMM | lld:pubmed |
pubmed-article:21762679 | pubmed:author | pubmed-author:ZhangDong-Qin... | lld:pubmed |
pubmed-article:21762679 | pubmed:author | pubmed-author:XuTie-JunTJ | lld:pubmed |
pubmed-article:21762679 | pubmed:author | pubmed-author:WangXiang-Zhe... | lld:pubmed |
pubmed-article:21762679 | pubmed:copyrightInfo | Crown Copyright © 2011. Published by Elsevier Inc. All rights reserved. | lld:pubmed |
pubmed-article:21762679 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21762679 | pubmed:day | 12 | lld:pubmed |
pubmed-article:21762679 | pubmed:volume | 411 | lld:pubmed |
pubmed-article:21762679 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21762679 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21762679 | pubmed:pagination | 667-72 | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:meshHeading | pubmed-meshheading:21762679... | lld:pubmed |
pubmed-article:21762679 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21762679 | pubmed:articleTitle | NR2B-containing NMDA receptors promote neural progenitor cell proliferation through CaMKIV/CREB pathway. | lld:pubmed |
pubmed-article:21762679 | pubmed:affiliation | Department of Anatomy and Neurobiology, Xuzhou Medical College, China. limeihit@163.com | lld:pubmed |
pubmed-article:21762679 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21762679 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:24410 | entrezgene:pubmed | pubmed-article:21762679 | lld:entrezgene |
entrez-gene:25050 | entrezgene:pubmed | pubmed-article:21762679 | lld:entrezgene |
entrez-gene:81646 | entrezgene:pubmed | pubmed-article:21762679 | lld:entrezgene |
http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21762679 | lld:entrezgene |
http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21762679 | lld:entrezgene |
http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21762679 | lld:entrezgene |