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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2009-10-20
pubmed:abstractText
In this study 8 genes of growth factors and their receptors were investigated that are known to play a significant role in signaling pathways involved in the ontogenetic, but also tumorigenic, development of breast and mammary glands. Differential expression of fibroblast growth factor receptor 2 (FGFR2), GH receptor (GHR), hepatocyte growth factor (HGF), hepatocyte growth factor receptor (HGFR), platelet-derived growth factor alpha (PDGFA), platelet-derived growth factor receptor alpha (PDGFRA), platelet-derived growth factor beta (PDGFB), and vascular endothelial growth factor (VEGF) was analyzed in mesenchymal and epithelial teat tissue of peripubertal pigs affected and nonaffected by the inverted teat defect. Comparisons were made at the level where pigs were affected between samples derived from nonaffected animals and affected animals, including specimens of normal and inverted teats. In addition, comparisons were made at the level of the teat phenotype with normal teats of nonaffected animals vs. either the normal or the inverted teat of affected animals. All genes tested, except HGFR, showed significant differential expression at P < 0.05 in the mesenchymal or the epithelial teat tissue or both. In general, we observed more pronounced differences when comparing samples obtained from inverted tissues vs. samples from normal ones. Therefore, results of our study suggest that gene expression of the growth factors and their receptors associates directly with the teat phenotype rather than with the affection status of the investigated animals, suggesting that local processes and tissue-specific compensation by means of differential expression of growth factors and their receptors are responsible for the development of impaired teat phenotypes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Growth Factor, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Platelet-Derived Growth Factor, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-met, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-sis, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Fibroblast Growth..., http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Platelet-Derived Growth..., http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Platelet-Derived Growth..., http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Growth Factor, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Somatotropin, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Vascular Endothelial..., http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor A, http://linkedlifedata.com/resource/pubmed/chemical/platelet-derived growth factor A
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1525-3163
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
87
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3451-7
pubmed:meshHeading
pubmed-meshheading:19648501-Animals, pubmed-meshheading:19648501-Female, pubmed-meshheading:19648501-Gene Expression Profiling, pubmed-meshheading:19648501-Hepatocyte Growth Factor, pubmed-meshheading:19648501-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:19648501-Male, pubmed-meshheading:19648501-Mammary Glands, Animal, pubmed-meshheading:19648501-Platelet-Derived Growth Factor, pubmed-meshheading:19648501-Proto-Oncogene Proteins c-met, pubmed-meshheading:19648501-Proto-Oncogene Proteins c-sis, pubmed-meshheading:19648501-Receptor, Fibroblast Growth Factor, Type 2, pubmed-meshheading:19648501-Receptor, Platelet-Derived Growth Factor alpha, pubmed-meshheading:19648501-Receptor, Platelet-Derived Growth Factor beta, pubmed-meshheading:19648501-Receptors, Growth Factor, pubmed-meshheading:19648501-Receptors, Somatotropin, pubmed-meshheading:19648501-Receptors, Vascular Endothelial Growth Factor, pubmed-meshheading:19648501-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:19648501-Sus scrofa, pubmed-meshheading:19648501-Swine Diseases, pubmed-meshheading:19648501-Vascular Endothelial Growth Factor A
pubmed:year
2009
pubmed:articleTitle
Differential expression of growth factors and their receptors indicates their involvement in the inverted teat defect in pigs.
pubmed:affiliation
Research Institute for the Biology of Farm Animals, Research Unit Molecular Biology, Wilhelm-Stahl-Allee 2, 18196 Dummerstorf, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't