Source:http://linkedlifedata.com/resource/pubmed/id/15591145
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
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| pubmed:dateCreated |
2005-2-16
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| pubmed:abstractText |
Glial erbB-1 and erbB-4 receptors are key components of the process by which neuroendocrine glial cells control LHRH secretion and the onset of female puberty. We now provide evidence that these two signaling systems work in a coordinated fashion to control reproductive function. To generate animals carrying functionally impaired erbB-1 and erbB-4 receptors, we crossed Waved 2 (Wa-2+/+) mice harboring a point mutation of the erbB-1 receptor with mice expressing a dominant-negative erbB-4 receptor in astrocytes. In comparison to single-deficient mice, double-mutant animals exhibited a further delay in the onset of puberty and a strikingly diminished adult reproductive capacity. Ligand-dependent erbB receptor phosphorylation and erbB-mediated MAPK (ERK 1/2) phosphorylation were impaired in mutant astrocytes. Wa-2+/+ or double-mutant astrocytes failed to respond to TGF alpha with production of prostaglandin E2, one of the factors mediating the stimulatory effect of astroglial erbB receptor activation on LHRH release. Medium conditioned by Wa-2+/+ or double-mutant astrocytes treated with TGF alpha failed to stimulate LHRH release from GT1-7 cells. The LH response to ovariectomy was significantly attenuated in mutant mice in comparison with wild-type controls. Although the Wa-2 mutation affects all cells bearing erbB-1 receptors, these results suggest that a major defect underlying the reproductive defects of animals with impaired erbB signaling is a decreased ability of glial cells to stimulate LHRH release. Thus, a coordinated involvement of erbB-1 and erbB-4 signaling systems is required for the normalcy of sexual development and the maintenance of mature female reproductive function.
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| pubmed:grant | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
AIM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Culture Media, Conditioned,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Luteinizing Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/receptor tyrosine-protein kinase...
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| pubmed:status |
MEDLINE
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| pubmed:month |
Mar
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| pubmed:issn |
0013-7227
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:volume |
146
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
1465-72
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| pubmed:dateRevised |
2011-11-2
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| pubmed:meshHeading |
pubmed-meshheading:15591145-Animals,
pubmed-meshheading:15591145-Astrocytes,
pubmed-meshheading:15591145-Blotting, Western,
pubmed-meshheading:15591145-Body Weight,
pubmed-meshheading:15591145-Brain,
pubmed-meshheading:15591145-Culture Media, Conditioned,
pubmed-meshheading:15591145-Dinoprostone,
pubmed-meshheading:15591145-Female,
pubmed-meshheading:15591145-Gene Expression Regulation, Developmental,
pubmed-meshheading:15591145-Genes, Dominant,
pubmed-meshheading:15591145-Homozygote,
pubmed-meshheading:15591145-Humans,
pubmed-meshheading:15591145-Immunoprecipitation,
pubmed-meshheading:15591145-Ligands,
pubmed-meshheading:15591145-Luteinizing Hormone,
pubmed-meshheading:15591145-MAP Kinase Signaling System,
pubmed-meshheading:15591145-Mice,
pubmed-meshheading:15591145-Mice, Mutant Strains,
pubmed-meshheading:15591145-Mice, Transgenic,
pubmed-meshheading:15591145-Mutation,
pubmed-meshheading:15591145-Neuroglia,
pubmed-meshheading:15591145-Ovary,
pubmed-meshheading:15591145-Phosphorylation,
pubmed-meshheading:15591145-Point Mutation,
pubmed-meshheading:15591145-Prostaglandins,
pubmed-meshheading:15591145-Receptor, Epidermal Growth Factor,
pubmed-meshheading:15591145-Signal Transduction
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| pubmed:year |
2005
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| pubmed:articleTitle |
erbB-1 and erbB-4 receptors act in concert to facilitate female sexual development and mature reproductive function.
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| pubmed:affiliation |
Division of Neuroscience, Oregon National Primate Research Center/Oregon Health & Sciences Unversity, 505 Northwest 185th Avenue, Beaverton, Oregon 97006, USA.
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| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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