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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 |
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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 & inhibitors ; Receptor, Epidermal Growth Factor - metabolism ; Receptor, ErbB-2 - antagonists & inhibitors ; Signal Transduction - drug effects ; Skin - drug effects ; Skin - growth & 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. All rights reserved. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c616t-d6e6f14875c82989ffaee161c6e5532b47d1c4da49bd2e8ba3c544c4b6948e083</citedby><cites>FETCH-LOGICAL-c616t-d6e6f14875c82989ffaee161c6e5532b47d1c4da49bd2e8ba3c544c4b6948e083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23706492$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Activation of the epidermal growth factor receptor promotes lymphangiogenesis in the skin</title><title>Journal of dermatological science</title><addtitle>J Dermatol Sci</addtitle><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.</description><subject>Amphiregulin</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Cell Differentiation - drug effects</subject><subject>Cells, Cultured</subject><subject>Dermatology</subject><subject>EGF</subject><subject>EGF Family of Proteins</subject><subject>EGF receptor</subject><subject>Embryoid Bodies - cytology</subject><subject>Embryoid Bodies - drug effects</subject><subject>Embryoid Bodies - metabolism</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Embryonic Stem Cells - drug effects</subject><subject>Embryonic Stem Cells - metabolism</subject><subject>Endothelial Cells - cytology</subject><subject>Endothelial Cells - drug effects</subject><subject>Endothelial Cells - metabolism</subject><subject>Epidermal Growth Factor - metabolism</subject><subject>Epidermal Growth Factor - pharmacology</subject><subject>Female</subject><subject>Glycoproteins - genetics</subject><subject>Glycoproteins - metabolism</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins - genetics</subject><subject>Intercellular Signaling Peptides and Proteins - metabolism</subject><subject>Lymphangiogenesis</subject><subject>Lymphangiogenesis - drug effects</subject><subject>Lymphangiogenesis - physiology</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Receptor, Epidermal Growth Factor - antagonists & inhibitors</subject><subject>Receptor, Epidermal Growth Factor - metabolism</subject><subject>Receptor, ErbB-2 - antagonists & inhibitors</subject><subject>Signal Transduction - drug effects</subject><subject>Skin - drug effects</subject><subject>Skin - growth & 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 ; Angehrn, Yvonne ; Klein, Sarah ; Riccardi, Sabrina ; Baenziger-Tobler, Nadja ; Otto, Vivianne I ; Pittelkow, Mark ; Detmar, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c616t-d6e6f14875c82989ffaee161c6e5532b47d1c4da49bd2e8ba3c544c4b6948e083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Amphiregulin</topic><topic>Angiogenesis</topic><topic>Animals</topic><topic>Cell Differentiation - drug effects</topic><topic>Cells, Cultured</topic><topic>Dermatology</topic><topic>EGF</topic><topic>EGF Family of Proteins</topic><topic>EGF receptor</topic><topic>Embryoid Bodies - cytology</topic><topic>Embryoid Bodies - drug effects</topic><topic>Embryoid Bodies - metabolism</topic><topic>Embryonic Stem Cells - cytology</topic><topic>Embryonic Stem Cells - drug effects</topic><topic>Embryonic Stem Cells - metabolism</topic><topic>Endothelial Cells - cytology</topic><topic>Endothelial Cells - drug effects</topic><topic>Endothelial Cells - metabolism</topic><topic>Epidermal Growth Factor - metabolism</topic><topic>Epidermal Growth Factor - pharmacology</topic><topic>Female</topic><topic>Glycoproteins - genetics</topic><topic>Glycoproteins - metabolism</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins - genetics</topic><topic>Intercellular Signaling Peptides and Proteins - metabolism</topic><topic>Lymphangiogenesis</topic><topic>Lymphangiogenesis - drug effects</topic><topic>Lymphangiogenesis - physiology</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Receptor, Epidermal Growth Factor - antagonists & inhibitors</topic><topic>Receptor, Epidermal Growth Factor - metabolism</topic><topic>Receptor, ErbB-2 - antagonists & inhibitors</topic><topic>Signal Transduction - drug effects</topic><topic>Skin - drug effects</topic><topic>Skin - growth & 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. 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.</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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