Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2002-4-23
pubmed:abstractText
Phenotypically and functionally different types of microvascular endothelial cells (MVECs) derived from the developing corpus luteum were isolated and characterized by our group. We investigated whether these cytokeratin-positive (CK+) and cytokeratin-negative (CK-) MVECs differed in the expression of angiogenic factors and their regulation under hypoxia. Using quantitative RT-PCR, VEGF and its receptors, Flk-1 and Flt-1, were detected in CK- MVECs. The mRNA expression of Flk-1 mRNA was 100 times as high as that of Flt-1 mRNA. CK+ MVECs expressed VEGF and Flt-1 mRNA, but were devoid of Flk-1 transcripts. No Ang-1 mRNA was demonstrated in either cell type, and Ang-2 mRNA was found only in CK- MVECs. Tie-2 mRNA was detected in both MVEC types, but levels were 150 times as high in CK- MVECs as in CK+ MVECs. mRNA of hypoxia-inducible factors Hif-1alpha and Hif-1beta was expressed in both MVEC types. After hypoxia, neither VEGF, nor Flk-1, nor Tie-2 mRNA expression was altered in either MVEC type. Flt-1 expression and Ang-2 mRNA expression were significantly increased at about 2.5-fold (P < 0.05) in CK- MVECs, but not in CK+ MVECs. Our study demonstrates the varying expression and regulation of angiogenesis-related factors and receptors in phenotypically different MVEC types.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ARNT protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Angiopoietin-1, http://linkedlifedata.com/resource/pubmed/chemical/Angiopoietin-2, http://linkedlifedata.com/resource/pubmed/chemical/Aryl Hydrocarbon Receptor Nuclear..., http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/FLT3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Keratins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, TIE-2, http://linkedlifedata.com/resource/pubmed/chemical/Receptor Protein-Tyrosine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Aryl Hydrocarbon, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine, http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor..., http://linkedlifedata.com/resource/pubmed/chemical/fms-Like Tyrosine Kinase 3
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0026-2862
pubmed:author
pubmed:copyrightInfo
(c) 2002 Elsevier Science (USA).
pubmed:issnType
Print
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
243-51
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11969301-Angiopoietin-1, pubmed-meshheading:11969301-Angiopoietin-2, pubmed-meshheading:11969301-Animals, pubmed-meshheading:11969301-Anoxia, pubmed-meshheading:11969301-Aryl Hydrocarbon Receptor Nuclear Translocator, pubmed-meshheading:11969301-Binding, Competitive, pubmed-meshheading:11969301-Blotting, Western, pubmed-meshheading:11969301-Cattle, pubmed-meshheading:11969301-Cells, Cultured, pubmed-meshheading:11969301-Cloning, Molecular, pubmed-meshheading:11969301-Corpus Luteum, pubmed-meshheading:11969301-DNA, Complementary, pubmed-meshheading:11969301-DNA-Binding Proteins, pubmed-meshheading:11969301-Endothelium, Vascular, pubmed-meshheading:11969301-Female, pubmed-meshheading:11969301-Humans, pubmed-meshheading:11969301-Keratins, pubmed-meshheading:11969301-Membrane Glycoproteins, pubmed-meshheading:11969301-Neovascularization, Pathologic, pubmed-meshheading:11969301-Phenotype, pubmed-meshheading:11969301-Phosphorylation, pubmed-meshheading:11969301-Precipitin Tests, pubmed-meshheading:11969301-Protein Biosynthesis, pubmed-meshheading:11969301-Proto-Oncogene Proteins, pubmed-meshheading:11969301-RNA, pubmed-meshheading:11969301-RNA, Messenger, pubmed-meshheading:11969301-Receptor, TIE-2, pubmed-meshheading:11969301-Receptor Protein-Tyrosine Kinases, pubmed-meshheading:11969301-Receptors, Aryl Hydrocarbon, pubmed-meshheading:11969301-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:11969301-Temperature, pubmed-meshheading:11969301-Transcription Factors, pubmed-meshheading:11969301-Tyrosine, pubmed-meshheading:11969301-Vascular Endothelial Growth Factor Receptor-1, pubmed-meshheading:11969301-fms-Like Tyrosine Kinase 3
pubmed:year
2002
pubmed:articleTitle
Microvascular endothelial cells differ in basal and hypoxia-regulated expression of angiogenic factors and their receptors.
pubmed:affiliation
Institute of Anatomy, Institute of Pharmacy, University of Leipzig, Liebigstrasse 13, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't