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Activation of the epidermal growth factor receptor promotes lymphangiogenesis in the skin

Abstract Background The lymphatic vascular system regulates tissue fluid homeostasis and plays important roles in immune surveillance, inflammation and cancer metastasis. However, the molecular mechanisms involved in the regulation of lymphangiogenesis remain incompletely characterized. Objective We...

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Published in:Journal of dermatological science 2013-09, Vol.71 (3), p.184-194
Main Authors: Marino, Daniela, Angehrn, Yvonne, Klein, Sarah, Riccardi, Sabrina, Baenziger-Tobler, Nadja, Otto, Vivianne I, Pittelkow, Mark, Detmar, Michael
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cited_by cdi_FETCH-LOGICAL-c616t-d6e6f14875c82989ffaee161c6e5532b47d1c4da49bd2e8ba3c544c4b6948e083
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container_title Journal of dermatological science
container_volume 71
creator Marino, Daniela
Angehrn, Yvonne
Klein, Sarah
Riccardi, Sabrina
Baenziger-Tobler, Nadja
Otto, Vivianne I
Pittelkow, Mark
Detmar, Michael
description Abstract Background The lymphatic vascular system regulates tissue fluid homeostasis and plays important roles in immune surveillance, inflammation and cancer metastasis. However, the molecular mechanisms involved in the regulation of lymphangiogenesis remain incompletely characterized. Objective We aimed to identify new pathways involved in the promotion of skin lymphangiogenesis. Methods We used a mouse embryonic stem cell-derived embryoid body vascular differentiation assay to investigate the effects of a selection of pharmacological agents with the potential to inhibit blood and/or lymphatic vessel formation. We also used a subcutaneous Matrigel assay to study candidate lymphangiogenesis factors as well as skin-specific transgenic mice. Results We found that compounds inhibiting the epidermal growth factor (EGF) receptor (EGFR) led to an impaired formation of lymphatic vessel-like structures. In vitro studies with human dermal lymphatic endothelial cells (LECs), that were found to express EGFR, revealed that EGF promotes lymphatic vessel formation. This effect was inhibited by EGFR-blocking antibodies and by low molecular weight inhibitors of the EGFR associated tyrosine kinase. Incorporation of EGF into a mouse matrigel plug assay showed that EGF promotes enlargement of lymphatic vessels in the skin in vivo. Moreover, transgenic mice with skin-specific overexpression of amphiregulin, another agonistic ligand of the EGFR, displayed an enhanced size and density of lymphatic vessels in the skin. Conclusion These findings reveal that EGFR activation is involved in lymphatic remodeling and suggest that specific EGFR antagonists might be used to inhibit pathological lymphangiogenesis.
doi_str_mv 10.1016/j.jdermsci.2013.04.024
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However, the molecular mechanisms involved in the regulation of lymphangiogenesis remain incompletely characterized. Objective We aimed to identify new pathways involved in the promotion of skin lymphangiogenesis. Methods We used a mouse embryonic stem cell-derived embryoid body vascular differentiation assay to investigate the effects of a selection of pharmacological agents with the potential to inhibit blood and/or lymphatic vessel formation. We also used a subcutaneous Matrigel assay to study candidate lymphangiogenesis factors as well as skin-specific transgenic mice. Results We found that compounds inhibiting the epidermal growth factor (EGF) receptor (EGFR) led to an impaired formation of lymphatic vessel-like structures. In vitro studies with human dermal lymphatic endothelial cells (LECs), that were found to express EGFR, revealed that EGF promotes lymphatic vessel formation. This effect was inhibited by EGFR-blocking antibodies and by low molecular weight inhibitors of the EGFR associated tyrosine kinase. Incorporation of EGF into a mouse matrigel plug assay showed that EGF promotes enlargement of lymphatic vessels in the skin in vivo. Moreover, transgenic mice with skin-specific overexpression of amphiregulin, another agonistic ligand of the EGFR, displayed an enhanced size and density of lymphatic vessels in the skin. Conclusion These findings reveal that EGFR activation is involved in lymphatic remodeling and suggest that specific EGFR antagonists might be used to inhibit pathological lymphangiogenesis.</description><identifier>ISSN: 0923-1811</identifier><identifier>EISSN: 1873-569X</identifier><identifier>DOI: 10.1016/j.jdermsci.2013.04.024</identifier><identifier>PMID: 23706492</identifier><language>eng</language><publisher>Netherlands: Elsevier Ireland Ltd</publisher><subject>Amphiregulin ; Angiogenesis ; Animals ; Cell Differentiation - drug effects ; Cells, Cultured ; Dermatology ; EGF ; EGF Family of Proteins ; EGF receptor ; Embryoid Bodies - cytology ; Embryoid Bodies - drug effects ; Embryoid Bodies - metabolism ; Embryonic Stem Cells - cytology ; Embryonic Stem Cells - drug effects ; Embryonic Stem Cells - metabolism ; Endothelial Cells - cytology ; Endothelial Cells - drug effects ; Endothelial Cells - metabolism ; Epidermal Growth Factor - metabolism ; Epidermal Growth Factor - pharmacology ; Female ; Glycoproteins - genetics ; Glycoproteins - metabolism ; Humans ; Intercellular Signaling Peptides and Proteins - genetics ; Intercellular Signaling Peptides and Proteins - metabolism ; Lymphangiogenesis ; Lymphangiogenesis - drug effects ; Lymphangiogenesis - physiology ; Mice ; Mice, Transgenic ; Receptor, Epidermal Growth Factor - antagonists &amp; inhibitors ; Receptor, Epidermal Growth Factor - metabolism ; Receptor, ErbB-2 - antagonists &amp; inhibitors ; Signal Transduction - drug effects ; Skin - drug effects ; Skin - growth &amp; development ; Skin - metabolism</subject><ispartof>Journal of dermatological science, 2013-09, Vol.71 (3), p.184-194</ispartof><rights>Japanese Society for Investigative Dermatology</rights><rights>2013 Japanese Society for Investigative Dermatology</rights><rights>Copyright © 2013 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.</rights><rights>2013 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. 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However, the molecular mechanisms involved in the regulation of lymphangiogenesis remain incompletely characterized. Objective We aimed to identify new pathways involved in the promotion of skin lymphangiogenesis. Methods We used a mouse embryonic stem cell-derived embryoid body vascular differentiation assay to investigate the effects of a selection of pharmacological agents with the potential to inhibit blood and/or lymphatic vessel formation. We also used a subcutaneous Matrigel assay to study candidate lymphangiogenesis factors as well as skin-specific transgenic mice. Results We found that compounds inhibiting the epidermal growth factor (EGF) receptor (EGFR) led to an impaired formation of lymphatic vessel-like structures. In vitro studies with human dermal lymphatic endothelial cells (LECs), that were found to express EGFR, revealed that EGF promotes lymphatic vessel formation. This effect was inhibited by EGFR-blocking antibodies and by low molecular weight inhibitors of the EGFR associated tyrosine kinase. Incorporation of EGF into a mouse matrigel plug assay showed that EGF promotes enlargement of lymphatic vessels in the skin in vivo. Moreover, transgenic mice with skin-specific overexpression of amphiregulin, another agonistic ligand of the EGFR, displayed an enhanced size and density of lymphatic vessels in the skin. 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inhibitors</subject><subject>Receptor, Epidermal Growth Factor - metabolism</subject><subject>Receptor, ErbB-2 - antagonists &amp; inhibitors</subject><subject>Signal Transduction - drug effects</subject><subject>Skin - drug effects</subject><subject>Skin - growth &amp; development</subject><subject>Skin - metabolism</subject><issn>0923-1811</issn><issn>1873-569X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkk1v1DAQhi1ERZeFv1DlyCWpv-LEl4qqKi1SJQ4FCU6W40x2nSZ2sL2L9t83YdsKuHCyJb_zjDXPIHRGcEEwEed90bcQxmhsQTFhBeYFpvwVWpG6Ynkp5PfXaIUlZTmpCTlFb2PsMcYl5fINOqWswoJLukI_Lk2ye52sd5nvsrSFDCa7oPWQbYL_lbZZp03yIQtgYFouU_CjTxCz4TBOW-021m_AQbQxs-43Ij5Y9w6ddHqI8P7pXKNvn66_Xt3md19uPl9d3uVGEJHyVoDoCK-r0tRU1rLrNAARxAgoS0YbXrXE8FZz2bQU6kYzU3JueCMkrwHXbI0ujtxp14zQGnAp6EFNwY46HJTXVv394uxWbfxesYqX1TytNfrwBAj-5w5iUqONBoZBO_C7qAinAmMhsZyj4hg1wccYoHtpQ7BavKhePXtRixeFuZq9zIVnf37ypexZxBz4eAzAPKq9haBmBDgDrZ3nnlTr7f97XPyDMIN11ujhAQ4Qe78LbhahiIpUYXW_bMeyHIRhTDiv2SNjN7pB</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Marino, Daniela</creator><creator>Angehrn, Yvonne</creator><creator>Klein, Sarah</creator><creator>Riccardi, Sabrina</creator><creator>Baenziger-Tobler, Nadja</creator><creator>Otto, Vivianne I</creator><creator>Pittelkow, Mark</creator><creator>Detmar, Michael</creator><general>Elsevier Ireland Ltd</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><scope>5PM</scope></search><sort><creationdate>20130901</creationdate><title>Activation of the epidermal growth factor receptor promotes lymphangiogenesis in the skin</title><author>Marino, Daniela ; 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inhibitors</topic><topic>Receptor, Epidermal Growth Factor - metabolism</topic><topic>Receptor, ErbB-2 - antagonists &amp; inhibitors</topic><topic>Signal Transduction - drug effects</topic><topic>Skin - drug effects</topic><topic>Skin - growth &amp; development</topic><topic>Skin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marino, Daniela</creatorcontrib><creatorcontrib>Angehrn, Yvonne</creatorcontrib><creatorcontrib>Klein, Sarah</creatorcontrib><creatorcontrib>Riccardi, Sabrina</creatorcontrib><creatorcontrib>Baenziger-Tobler, Nadja</creatorcontrib><creatorcontrib>Otto, Vivianne I</creatorcontrib><creatorcontrib>Pittelkow, Mark</creatorcontrib><creatorcontrib>Detmar, Michael</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of dermatological science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marino, Daniela</au><au>Angehrn, Yvonne</au><au>Klein, Sarah</au><au>Riccardi, Sabrina</au><au>Baenziger-Tobler, Nadja</au><au>Otto, Vivianne I</au><au>Pittelkow, Mark</au><au>Detmar, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activation of the epidermal growth factor receptor promotes lymphangiogenesis in the skin</atitle><jtitle>Journal of dermatological science</jtitle><addtitle>J Dermatol Sci</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>71</volume><issue>3</issue><spage>184</spage><epage>194</epage><pages>184-194</pages><issn>0923-1811</issn><eissn>1873-569X</eissn><abstract>Abstract Background The lymphatic vascular system regulates tissue fluid homeostasis and plays important roles in immune surveillance, inflammation and cancer metastasis. 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This effect was inhibited by EGFR-blocking antibodies and by low molecular weight inhibitors of the EGFR associated tyrosine kinase. Incorporation of EGF into a mouse matrigel plug assay showed that EGF promotes enlargement of lymphatic vessels in the skin in vivo. Moreover, transgenic mice with skin-specific overexpression of amphiregulin, another agonistic ligand of the EGFR, displayed an enhanced size and density of lymphatic vessels in the skin. Conclusion These findings reveal that EGFR activation is involved in lymphatic remodeling and suggest that specific EGFR antagonists might be used to inhibit pathological lymphangiogenesis.</abstract><cop>Netherlands</cop><pub>Elsevier Ireland Ltd</pub><pmid>23706492</pmid><doi>10.1016/j.jdermsci.2013.04.024</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Amphiregulin
Angiogenesis
Animals
Cell Differentiation - drug effects
Cells, Cultured
Dermatology
EGF
EGF Family of Proteins
EGF receptor
Embryoid Bodies - cytology
Embryoid Bodies - drug effects
Embryoid Bodies - metabolism
Embryonic Stem Cells - cytology
Embryonic Stem Cells - drug effects
Embryonic Stem Cells - metabolism
Endothelial Cells - cytology
Endothelial Cells - drug effects
Endothelial Cells - metabolism
Epidermal Growth Factor - metabolism
Epidermal Growth Factor - pharmacology
Female
Glycoproteins - genetics
Glycoproteins - metabolism
Humans
Intercellular Signaling Peptides and Proteins - genetics
Intercellular Signaling Peptides and Proteins - metabolism
Lymphangiogenesis
Lymphangiogenesis - drug effects
Lymphangiogenesis - physiology
Mice
Mice, Transgenic
Receptor, Epidermal Growth Factor - antagonists & inhibitors
Receptor, Epidermal Growth Factor - metabolism
Receptor, ErbB-2 - antagonists & inhibitors
Signal Transduction - drug effects
Skin - drug effects
Skin - growth & development
Skin - metabolism
title Activation of the epidermal growth factor receptor promotes lymphangiogenesis in the skin
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