Source:http://linkedlifedata.com/resource/pubmed/id/20937356
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
|
pubmed:dateCreated |
2010-12-28
|
pubmed:abstractText |
GnRH neurons provide the primary driving force upon the neuroendocrine reproductive axis. Here we used GnV-3 cells, a model of conditionally immortalized GnRH-expressing neurons, to perform an analysis of cell cycle and compare the gene expression profile of proliferating cells with differentiated cells. In the proliferation medium, 45 ± 1.5% of GnV-3 cells are in S-phase by FACS analysis. In the differentiation medium, only 9 ± 0.9% of them are in S-phase, and they acquire the characteristic bipolar shape displayed by preoptic GnRH neurons in vivo. In addition, GnV-3 cells in the differentiated state exhibit electrophysiological properties characteristic of neurons. Transcriptomic analysis identified up-regulation of 1931 genes and down-regulation of 1270 genes in cells grown in the differentiation medium compared to cells in the proliferation medium. Subsequent gene ontology study indicated that genes over-expressed in proliferating GnV-3 cells were mainly involved in cell cycle regulations, whereas genes over-expressed in differentiated cells were mainly involved in processes of differentiation, neurogenesis and neuronal morphogenesis. Taken together, these data demonstrate the occurrence of morphological and physiological changes in GnV-3 cells between the proliferating and the differentiated state. Moreover, the genes differentially regulated between these two different states are providing novel pathways potentially important for a better understanding of the physiology of mature GnRH neurons.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
1872-8057
|
pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.
|
pubmed:issnType |
Electronic
|
pubmed:day |
30
|
pubmed:volume |
332
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
97-105
|
pubmed:meshHeading |
pubmed-meshheading:20937356-Animals,
pubmed-meshheading:20937356-Cell Cycle,
pubmed-meshheading:20937356-Cell Differentiation,
pubmed-meshheading:20937356-Cell Line,
pubmed-meshheading:20937356-Cell Proliferation,
pubmed-meshheading:20937356-Cell Shape,
pubmed-meshheading:20937356-Gene Expression Profiling,
pubmed-meshheading:20937356-Gonadotropin-Releasing Hormone,
pubmed-meshheading:20937356-Microarray Analysis,
pubmed-meshheading:20937356-Neurons,
pubmed-meshheading:20937356-Neuropilin-1,
pubmed-meshheading:20937356-Patch-Clamp Techniques,
pubmed-meshheading:20937356-Phenotype,
pubmed-meshheading:20937356-Rats
|
pubmed:year |
2011
|
pubmed:articleTitle |
Phenotypic and molecular characterization of proliferating and differentiated GnRH-expressing GnV-3 cells.
|
pubmed:affiliation |
Service of Endocrinology, Diabetology and Metabolism, University Hospital and Faculty of Biology and Medicine, 1011 Lausanne, Switzerland.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|