pubmed-article:17440958 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0007600 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C1882071 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0034721 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0034693 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0007589 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0004112 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0007595 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0314603 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C0237477 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C1314939 | lld:lifeskim |
pubmed-article:17440958 | lifeskim:mentions | umls-concept:C1511938 | lld:lifeskim |
pubmed-article:17440958 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:17440958 | pubmed:dateCreated | 2007-11-26 | lld:pubmed |
pubmed-article:17440958 | pubmed:abstractText | The purpose of the present study is to establish and characterize a conditionally immortalized astrocyte cell line and to clarify the genetic networks responsible for the cell growth arrest and differentiation. A conditionally immortalized astrocyte cell line, RCG-12, was established by infecting primary cultured rat cortical glia cells with a temperature-sensitive simian virus 40 large T-antigen. At a permissive temperature of 33 degrees C, the large T-antigen was expressed and cells grew continuously. On the other hand, the down-regulation of T-antigen at a non-permissive temperature of 39 degrees C led to growth arrest and differentiation. The cells expressed astrocyte-expressed genes such as glial fibrillary acidic protein. Interestingly, the differentiated condition induced by the non-permissive temperature significantly elevated the expression levels of several astrocyte-expressed genes. To identify the detailed mechanisms by which non-permissive temperature-induced cell growth arrest and differentiation, we performed high-density oligonucleotide microarray analysis and found that 556 out of 15,923 probe sets were differentially expressed 2.0-fold. A computational gene network analysis revealed that a genetic network containing up-regulated genes such as RB, NOTCH1, and CDKN1A was associated with the cellular growth and proliferation, and that a genetic network containing down-regulated genes such as MYC, CCNB1, and IGF1 was associated with the cell cycle. The established cell line RCG-12 retains some characteristics of astrocytes and should provide an excellent model for studies of astrocyte biology. The present results will also provide a basis for understanding the detailed molecular mechanisms of the growth arrest and differentiation of astrocytes. | lld:pubmed |
pubmed-article:17440958 | pubmed:language | eng | lld:pubmed |
pubmed-article:17440958 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17440958 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17440958 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17440958 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17440958 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17440958 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17440958 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17440958 | pubmed:month | Dec | lld:pubmed |
pubmed-article:17440958 | pubmed:issn | 0730-2312 | lld:pubmed |
pubmed-article:17440958 | pubmed:author | pubmed-author:TsudaMasaakiM | lld:pubmed |
pubmed-article:17440958 | pubmed:author | pubmed-author:TabuchiYoshia... | lld:pubmed |
pubmed-article:17440958 | pubmed:author | pubmed-author:TakasakiIchir... | lld:pubmed |
pubmed-article:17440958 | pubmed:author | pubmed-author:YasudaMakotoM | lld:pubmed |
pubmed-article:17440958 | pubmed:author | pubmed-author:FukuchiMamoru... | lld:pubmed |
pubmed-article:17440958 | pubmed:author | pubmed-author:TakaradaSatok... | lld:pubmed |
pubmed-article:17440958 | pubmed:copyrightInfo | Copyright (c) 2007 Wiley-Liss, Inc. | lld:pubmed |
pubmed-article:17440958 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17440958 | pubmed:day | 15 | lld:pubmed |
pubmed-article:17440958 | pubmed:volume | 102 | lld:pubmed |
pubmed-article:17440958 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17440958 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17440958 | pubmed:pagination | 1472-85 | lld:pubmed |
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pubmed-article:17440958 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17440958 | pubmed:articleTitle | Identification of genetic networks involved in the cell growth arrest and differentiation of a rat astrocyte cell line RCG-12. | lld:pubmed |
pubmed-article:17440958 | pubmed:affiliation | Division of Molecular Genetics Research, Life Science Research Center, University of Toyama, Sugitani 2630, Toyama 930-0194, Japan. takasaki@cts.u-toyama.ac.jp | lld:pubmed |
pubmed-article:17440958 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17440958 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:17440958 | lld:pubmed |