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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 |
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creator | 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 |
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</creator><creatorcontrib>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</creatorcontrib><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.</description><identifier>ISSN: 1058-8388</identifier><identifier>EISSN: 1097-0177</identifier><identifier>DOI: 10.1002/1097-0177(200007)218:3<507::AID-DVDY1012>3.0.CO;2-5</identifier><identifier>PMID: 10878616</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>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</subject><ispartof>Developmental dynamics, 2000-07, Vol.218 (3), p.507-524</ispartof><rights>Copyright © 2000 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5062-f0dd3a176c45285b793449209d3c7700dc655ab25535f2ccb2d52b8910c8aa063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10878616$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pepper, Michael S.</creatorcontrib><creatorcontrib>Baetens, Danielle</creatorcontrib><creatorcontrib>Mandriota, Stefano J.</creatorcontrib><creatorcontrib>Di Sanza, Corinne</creatorcontrib><creatorcontrib>Oikemus, Sarah</creatorcontrib><creatorcontrib>Lane, Timothy F.</creatorcontrib><creatorcontrib>Soriano, Jesus V.</creatorcontrib><creatorcontrib>Montesano, Roberto</creatorcontrib><creatorcontrib>Iruela‐Arispe, M. 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. 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.</description><subject>Adult</subject><subject>Amino Acid Sequence</subject><subject>angiogenesis</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Blotting, Northern</subject><subject>breast</subject><subject>Capillaries - growth & development</subject><subject>Capillaries - physiology</subject><subject>Cell Line</subject><subject>Endothelial Growth Factors - genetics</subject><subject>Endothelial Growth Factors - immunology</subject><subject>Endothelial Growth Factors - metabolism</subject><subject>Female</subject><subject>Gene Expression Regulation - physiology</subject><subject>growth factor</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Lactation - genetics</subject><subject>Lactation - physiology</subject><subject>Lymphokines - genetics</subject><subject>Lymphokines - immunology</subject><subject>Lymphokines - metabolism</subject><subject>Mammary Glands, Animal - anatomy & histology</subject><subject>Mammary Glands, Animal - blood supply</subject><subject>Mammary Glands, Animal - physiology</subject><subject>Mice</subject><subject>Milk, Human - chemistry</subject><subject>Molecular Sequence Data</subject><subject>Neovascularization, Physiologic</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Receptor Protein-Tyrosine Kinases - genetics</subject><subject>Receptor Protein-Tyrosine Kinases - immunology</subject><subject>Receptor Protein-Tyrosine Kinases - metabolism</subject><subject>Receptors, Growth Factor - genetics</subject><subject>Receptors, Growth Factor - immunology</subject><subject>Receptors, Growth Factor - metabolism</subject><subject>Receptors, Vascular Endothelial Growth Factor</subject><subject>RNA - isolation & purification</subject><subject>RNA - metabolism</subject><subject>Sequence Alignment</subject><subject>Vascular Endothelial Growth Factor A</subject><subject>Vascular Endothelial Growth Factor C</subject><subject>Vascular Endothelial Growth Factors</subject><subject>vascular permeability</subject><subject>Weaning</subject><issn>1058-8388</issn><issn>1097-0177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqVkU1P3DAQhi3UCijtX6h8qlqJbMd2HDsLqoR2gSIhrdQW1J4sx3aWoHxs7aR0_30dAogLh_rimdE779jzIHREYEYA6GcCuUiACPGRQjziEyVyzo45iPn85GKZLK-XvwgQ-oXNYLZYHdGE76D9p65XY8xlIpmUe-hNCLfRRGYp2UV7BKSQGcn20d03tx5q3Vddi7sSX5-en2Hd2inwzrhN33ns_m68C2EUVS3ubxz2nXVtjxvdNNpv8boem-zgq3aNo3bd6tZsD3GtTX9vfnjvWrV_unoY87fodanr4N493Afo6uz0x-Jrcrk6v1icXCaGQ0aTEqxlmojMpJxKXoicpWlOIbfMCAFgTca5LijnjJfUmIJaTguZEzBSa8jYAfow-W5893twoVdNFYyr43tdNwQlCKV5CjIKv09C47sQvCvVxlfj3xQBNfJQ42bVuFk18VCRh2Iq8lAq8lCPPGIN1GKlqOLR9f3D-KFonH3mOQGIgp-T4K6q3fZ_Zr4w8qnG_gGsRaSK</recordid><startdate>200007</startdate><enddate>200007</enddate><creator>Pepper, Michael S.</creator><creator>Baetens, Danielle</creator><creator>Mandriota, Stefano J.</creator><creator>Di Sanza, Corinne</creator><creator>Oikemus, Sarah</creator><creator>Lane, Timothy F.</creator><creator>Soriano, Jesus V.</creator><creator>Montesano, Roberto</creator><creator>Iruela‐Arispe, M. Luisa</creator><general>John Wiley & Sons, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200007</creationdate><title>Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involution</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5062-f0dd3a176c45285b793449209d3c7700dc655ab25535f2ccb2d52b8910c8aa063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adult</topic><topic>Amino Acid Sequence</topic><topic>angiogenesis</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Blotting, Northern</topic><topic>breast</topic><topic>Capillaries - growth & development</topic><topic>Capillaries - physiology</topic><topic>Cell Line</topic><topic>Endothelial Growth Factors - genetics</topic><topic>Endothelial Growth Factors - immunology</topic><topic>Endothelial Growth Factors - metabolism</topic><topic>Female</topic><topic>Gene Expression Regulation - physiology</topic><topic>growth factor</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization</topic><topic>Lactation - genetics</topic><topic>Lactation - physiology</topic><topic>Lymphokines - genetics</topic><topic>Lymphokines - immunology</topic><topic>Lymphokines - metabolism</topic><topic>Mammary Glands, Animal - anatomy & histology</topic><topic>Mammary Glands, Animal - blood supply</topic><topic>Mammary Glands, Animal - physiology</topic><topic>Mice</topic><topic>Milk, Human - chemistry</topic><topic>Molecular Sequence Data</topic><topic>Neovascularization, Physiologic</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Receptor Protein-Tyrosine Kinases - genetics</topic><topic>Receptor Protein-Tyrosine Kinases - immunology</topic><topic>Receptor Protein-Tyrosine Kinases - metabolism</topic><topic>Receptors, Growth Factor - genetics</topic><topic>Receptors, Growth Factor - immunology</topic><topic>Receptors, Growth Factor - metabolism</topic><topic>Receptors, Vascular Endothelial Growth Factor</topic><topic>RNA - isolation & purification</topic><topic>RNA - metabolism</topic><topic>Sequence Alignment</topic><topic>Vascular Endothelial Growth Factor A</topic><topic>Vascular Endothelial Growth Factor C</topic><topic>Vascular Endothelial Growth Factors</topic><topic>vascular permeability</topic><topic>Weaning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pepper, Michael S.</creatorcontrib><creatorcontrib>Baetens, Danielle</creatorcontrib><creatorcontrib>Mandriota, Stefano J.</creatorcontrib><creatorcontrib>Di Sanza, Corinne</creatorcontrib><creatorcontrib>Oikemus, Sarah</creatorcontrib><creatorcontrib>Lane, Timothy F.</creatorcontrib><creatorcontrib>Soriano, Jesus V.</creatorcontrib><creatorcontrib>Montesano, Roberto</creatorcontrib><creatorcontrib>Iruela‐Arispe, M. Luisa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental dynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pepper, Michael S.</au><au>Baetens, Danielle</au><au>Mandriota, Stefano J.</au><au>Di Sanza, Corinne</au><au>Oikemus, Sarah</au><au>Lane, Timothy F.</au><au>Soriano, Jesus V.</au><au>Montesano, Roberto</au><au>Iruela‐Arispe, M. Luisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of VEGF and VEGF receptor expression in the rodent mammary gland during pregnancy, lactation, and involution</atitle><jtitle>Developmental dynamics</jtitle><addtitle>Dev Dyn</addtitle><date>2000-07</date><risdate>2000</risdate><volume>218</volume><issue>3</issue><spage>507</spage><epage>524</epage><pages>507-524</pages><issn>1058-8388</issn><eissn>1097-0177</eissn><abstract>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.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10878616</pmid><doi>10.1002/1097-0177(200007)218:3<507::AID-DVDY1012>3.0.CO;2-5</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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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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