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Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involution

Vascular endothelial growth factors (VEGFs) are endothelial cell‐specific mitogens with potent angiogenic and vascular permeability‐inducing properties. VEGF, VEGF‐C, and VEGFRs ‐1, ‐2, and ‐3 were found to be expressed in post‐pubertal (virgin) rodent mammary glands. VEGF was increased during pregn...

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Published in:Developmental dynamics 2000-07, Vol.218 (3), p.507-524
Main Authors: Pepper, Michael S., Baetens, Danielle, Mandriota, Stefano J., Di Sanza, Corinne, Oikemus, Sarah, Lane, Timothy F., Soriano, Jesus V., Montesano, Roberto, Iruela‐Arispe, M. Luisa
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container_title Developmental dynamics
container_volume 218
creator Pepper, Michael S.
Baetens, Danielle
Mandriota, Stefano J.
Di Sanza, Corinne
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Lane, Timothy F.
Soriano, Jesus V.
Montesano, Roberto
Iruela‐Arispe, M. Luisa
description Vascular endothelial growth factors (VEGFs) are endothelial cell‐specific mitogens with potent angiogenic and vascular permeability‐inducing properties. VEGF, VEGF‐C, and VEGFRs ‐1, ‐2, and ‐3 were found to be expressed in post‐pubertal (virgin) rodent mammary glands. VEGF was increased during pregnancy (5‐fold) and lactation (15–19‐fold). VEGF‐C was moderately increased during pregnancy and lactation (2‐ and 3‐fold respectively). VEGF levels were reduced by approximately 75% in cleared mouse mammary glands devoid of epithelial components, demonstrating that although the epithelial component is the major source of VEGF, approximately 25% is derived from stroma. This was confirmed by the findings (a) that VEGF transcripts were expressed predominantly in ductal and alveolar epithelial cells, and (b) that VEGF protein was localized to ductal epithelial cells as well as to the stromal compartment including vascular structures. VEGF was detected in human milk. Finally, transcripts for VEGFRs ‐2 and ‐3 were increased 2–3‐fold during pregnancy, VEGFRs ‐1, ‐2 and ‐3 were increased 2‐4‐fold during lactation, and VEGFRs ‐2 and ‐3 were decreased by 20‐50% during involution. These results point to a causal role for the VEGF ligand‐receptor pairs in pregnancy‐associated angiogenesis in the mammary gland, and suggest that they may also regulate vascular permeability during lactation. Dev Dyn 2000;218:507–524. © 2000 Wiley‐Liss, Inc.
doi_str_mv 10.1002/1097-0177(200007)218:3<507::AID-DVDY1012>3.0.CO;2-5
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Luisa</creatorcontrib><title>Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involution</title><title>Developmental dynamics</title><addtitle>Dev Dyn</addtitle><description>Vascular endothelial growth factors (VEGFs) are endothelial cell‐specific mitogens with potent angiogenic and vascular permeability‐inducing properties. VEGF, VEGF‐C, and VEGFRs ‐1, ‐2, and ‐3 were found to be expressed in post‐pubertal (virgin) rodent mammary glands. VEGF was increased during pregnancy (5‐fold) and lactation (15–19‐fold). VEGF‐C was moderately increased during pregnancy and lactation (2‐ and 3‐fold respectively). VEGF levels were reduced by approximately 75% in cleared mouse mammary glands devoid of epithelial components, demonstrating that although the epithelial component is the major source of VEGF, approximately 25% is derived from stroma. 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source Wiley-Blackwell Read & Publish Collection
subjects Adult
Amino Acid Sequence
angiogenesis
Animals
Base Sequence
Blotting, Northern
breast
Capillaries - growth & development
Capillaries - physiology
Cell Line
Endothelial Growth Factors - genetics
Endothelial Growth Factors - immunology
Endothelial Growth Factors - metabolism
Female
Gene Expression Regulation - physiology
growth factor
Humans
Immunohistochemistry
In Situ Hybridization
Lactation - genetics
Lactation - physiology
Lymphokines - genetics
Lymphokines - immunology
Lymphokines - metabolism
Mammary Glands, Animal - anatomy & histology
Mammary Glands, Animal - blood supply
Mammary Glands, Animal - physiology
Mice
Milk, Human - chemistry
Molecular Sequence Data
Neovascularization, Physiologic
Pregnancy
Rats
Receptor Protein-Tyrosine Kinases - genetics
Receptor Protein-Tyrosine Kinases - immunology
Receptor Protein-Tyrosine Kinases - metabolism
Receptors, Growth Factor - genetics
Receptors, Growth Factor - immunology
Receptors, Growth Factor - metabolism
Receptors, Vascular Endothelial Growth Factor
RNA - isolation & purification
RNA - metabolism
Sequence Alignment
Vascular Endothelial Growth Factor A
Vascular Endothelial Growth Factor C
Vascular Endothelial Growth Factors
vascular permeability
Weaning
title Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involution
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