Vascular MADs: Two Novel MAD-Related Genes Selectively Inducible by Flow in Human Vascular Endothelium
Vascular endothelium is an important transducer and integrator of both humoral and biomechanical stimuli within the cardiovascular system. Utilizing a differential display approach, we have identified two genes, Smad6 and Smad7, encoding members of the MAD-related family of molecules, selectively in...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1997-08, Vol.94 (17), p.9314-9319 |
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creator | Topper, James N. Cai, Jiexing Qiu, Yubin Anderson, Keith R. Xu, Yong-Yao Deeds, James D. Feeley, Roslyn Gimeno, Carlos J. Woolf, Elizabeth A. Tayber, Olga Mays, Gail G. Sampson, Barbara A. Schoen, Frederick J. Gimbrone, Michael A. Falb, Dean |
description | Vascular endothelium is an important transducer and integrator of both humoral and biomechanical stimuli within the cardiovascular system. Utilizing a differential display approach, we have identified two genes, Smad6 and Smad7, encoding members of the MAD-related family of molecules, selectively induced in cultured human vascular endothelial cells by steady laminar shear stress, a physiologic fluid mechanical stimulus. MAD-related proteins are a recently identified family of intracellular proteins that are thought to be essential components in the signaling pathways of the serine/threonine kinase receptors of the transforming growth factor β superfamily. Smad6 and Smad7 possess unique structural features (compared with previously described MADs), and they can physically interact with each other, and, in the case of Smad6, with other known human MAD species, in endothelial cells. Transient expression of Smad6 or Smad7 in vascular endothelial cells inhibits the activation of a transfected reporter gene in response to both TGF-β and fluid mechanical stimulation. Both Smad6 and Smad7 exhibit a selective pattern of expression in human vascular endothelium in vivo as detected by immunohistochemistry and in situ hybridization. Thus, Smad6 and Smad7 constitute a novel class of MAD-related proteins, termed vascular MADs, that are induced by fluid mechanical forces and can modulate gene expression in response to both humoral and biomechanical stimulation in vascular endothelium. |
doi_str_mv | 10.1073/pnas.94.17.9314 |
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Utilizing a differential display approach, we have identified two genes, Smad6 and Smad7, encoding members of the MAD-related family of molecules, selectively induced in cultured human vascular endothelial cells by steady laminar shear stress, a physiologic fluid mechanical stimulus. MAD-related proteins are a recently identified family of intracellular proteins that are thought to be essential components in the signaling pathways of the serine/threonine kinase receptors of the transforming growth factor β superfamily. Smad6 and Smad7 possess unique structural features (compared with previously described MADs), and they can physically interact with each other, and, in the case of Smad6, with other known human MAD species, in endothelial cells. Transient expression of Smad6 or Smad7 in vascular endothelial cells inhibits the activation of a transfected reporter gene in response to both TGF-β and fluid mechanical stimulation. Both Smad6 and Smad7 exhibit a selective pattern of expression in human vascular endothelium in vivo as detected by immunohistochemistry and in situ hybridization. Thus, Smad6 and Smad7 constitute a novel class of MAD-related proteins, termed vascular MADs, that are induced by fluid mechanical forces and can modulate gene expression in response to both humoral and biomechanical stimulation in vascular endothelium.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.94.17.9314</identifier><identifier>PMID: 9256479</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Amino Acid Sequence ; Antibodies ; Biochemistry ; Biological Sciences ; Cells, Cultured ; Cellular biology ; DNA-Binding Proteins - biosynthesis ; DNA-Binding Proteins - genetics ; Endothelial cells ; Endothelium ; Endothelium, Vascular - physiology ; Gene Expression ; Genes ; Human umbilical vein endothelial cells ; Humans ; Identification ; Immunohistochemistry ; In Situ Hybridization ; Molecular Sequence Data ; Molecules ; Physiological stimulation ; Receptors ; Sequence Alignment ; Shear stress ; Signal Transduction - genetics ; Smad6 Protein ; Smad7 Protein ; Stress, Mechanical ; Trans-Activators</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (17), p.9314-9319</ispartof><rights>Copyright 1997 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Aug 19, 1997</rights><rights>Copyright © 1997, The National Academy of Sciences of the USA 1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/94/17.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/42601$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/42601$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9256479$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Topper, James N.</creatorcontrib><creatorcontrib>Cai, Jiexing</creatorcontrib><creatorcontrib>Qiu, Yubin</creatorcontrib><creatorcontrib>Anderson, Keith R.</creatorcontrib><creatorcontrib>Xu, Yong-Yao</creatorcontrib><creatorcontrib>Deeds, James D.</creatorcontrib><creatorcontrib>Feeley, Roslyn</creatorcontrib><creatorcontrib>Gimeno, Carlos J.</creatorcontrib><creatorcontrib>Woolf, Elizabeth A.</creatorcontrib><creatorcontrib>Tayber, Olga</creatorcontrib><creatorcontrib>Mays, Gail G.</creatorcontrib><creatorcontrib>Sampson, Barbara A.</creatorcontrib><creatorcontrib>Schoen, Frederick J.</creatorcontrib><creatorcontrib>Gimbrone, Michael A.</creatorcontrib><creatorcontrib>Falb, Dean</creatorcontrib><title>Vascular MADs: Two Novel MAD-Related Genes Selectively Inducible by Flow in Human Vascular Endothelium</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Vascular endothelium is an important transducer and integrator of both humoral and biomechanical stimuli within the cardiovascular system. Utilizing a differential display approach, we have identified two genes, Smad6 and Smad7, encoding members of the MAD-related family of molecules, selectively induced in cultured human vascular endothelial cells by steady laminar shear stress, a physiologic fluid mechanical stimulus. MAD-related proteins are a recently identified family of intracellular proteins that are thought to be essential components in the signaling pathways of the serine/threonine kinase receptors of the transforming growth factor β superfamily. Smad6 and Smad7 possess unique structural features (compared with previously described MADs), and they can physically interact with each other, and, in the case of Smad6, with other known human MAD species, in endothelial cells. Transient expression of Smad6 or Smad7 in vascular endothelial cells inhibits the activation of a transfected reporter gene in response to both TGF-β and fluid mechanical stimulation. Both Smad6 and Smad7 exhibit a selective pattern of expression in human vascular endothelium in vivo as detected by immunohistochemistry and in situ hybridization. Thus, Smad6 and Smad7 constitute a novel class of MAD-related proteins, termed vascular MADs, that are induced by fluid mechanical forces and can modulate gene expression in response to both humoral and biomechanical stimulation in vascular endothelium.</description><subject>Amino Acid Sequence</subject><subject>Antibodies</subject><subject>Biochemistry</subject><subject>Biological Sciences</subject><subject>Cells, Cultured</subject><subject>Cellular biology</subject><subject>DNA-Binding Proteins - biosynthesis</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Endothelial cells</subject><subject>Endothelium</subject><subject>Endothelium, Vascular - physiology</subject><subject>Gene Expression</subject><subject>Genes</subject><subject>Human umbilical vein endothelial cells</subject><subject>Humans</subject><subject>Identification</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>Molecular Sequence Data</subject><subject>Molecules</subject><subject>Physiological stimulation</subject><subject>Receptors</subject><subject>Sequence Alignment</subject><subject>Shear stress</subject><subject>Signal Transduction - genetics</subject><subject>Smad6 Protein</subject><subject>Smad7 Protein</subject><subject>Stress, Mechanical</subject><subject>Trans-Activators</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxS1EVZbCGQkJZHFoT1nG33HFpSr9kgpIULhaTuzQrBx7iZOW_e-bVVdbygFOo9H7zdPTPIReEZgTUOz9Mto813xO1Fwzwp-gGQFNCsk1PEUzAKqKklP-DD3PeQEAWpSwi3Y1FZIrPUPND5vrMdgefzr6mA_x1W3Cn9OND-u9-OqDHbzDZz76jL_54OuhncQVvohurNsqeFyt8GlIt7iN-HzsbMRbx5Po0nDtQzt2L9BOY0P2LzdzD30_Pbk6Pi8uv5xdHB9dFgum2VAwIlhVWqBOWOcdsRWruHVWirppakqtqDwI56pag9OOQVUCq22pwBIlRcP20Id73-VYdd7VPg69DWbZt53tVybZ1jxWYnttfqYbQxlRfDrf35z36dfo82C6Ntc-BBt9GrNRmoKWHP4LEglKSkon8N1f4CKNfZx-YCgQJoUQa7c3f6bext20NOlvN_rU9oPKDVFm3foEHPwTMM0YwuB_DxP5-p5c5CH1W5RTOaW5A1H-tis</recordid><startdate>19970819</startdate><enddate>19970819</enddate><creator>Topper, James N.</creator><creator>Cai, Jiexing</creator><creator>Qiu, Yubin</creator><creator>Anderson, Keith R.</creator><creator>Xu, Yong-Yao</creator><creator>Deeds, James D.</creator><creator>Feeley, Roslyn</creator><creator>Gimeno, Carlos J.</creator><creator>Woolf, Elizabeth A.</creator><creator>Tayber, Olga</creator><creator>Mays, Gail G.</creator><creator>Sampson, Barbara A.</creator><creator>Schoen, Frederick J.</creator><creator>Gimbrone, Michael A.</creator><creator>Falb, Dean</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><general>The National Academy of Sciences of the USA</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19970819</creationdate><title>Vascular MADs: Two Novel MAD-Related Genes Selectively Inducible by Flow in Human Vascular Endothelium</title><author>Topper, James N. ; 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Utilizing a differential display approach, we have identified two genes, Smad6 and Smad7, encoding members of the MAD-related family of molecules, selectively induced in cultured human vascular endothelial cells by steady laminar shear stress, a physiologic fluid mechanical stimulus. MAD-related proteins are a recently identified family of intracellular proteins that are thought to be essential components in the signaling pathways of the serine/threonine kinase receptors of the transforming growth factor β superfamily. Smad6 and Smad7 possess unique structural features (compared with previously described MADs), and they can physically interact with each other, and, in the case of Smad6, with other known human MAD species, in endothelial cells. Transient expression of Smad6 or Smad7 in vascular endothelial cells inhibits the activation of a transfected reporter gene in response to both TGF-β and fluid mechanical stimulation. Both Smad6 and Smad7 exhibit a selective pattern of expression in human vascular endothelium in vivo as detected by immunohistochemistry and in situ hybridization. Thus, Smad6 and Smad7 constitute a novel class of MAD-related proteins, termed vascular MADs, that are induced by fluid mechanical forces and can modulate gene expression in response to both humoral and biomechanical stimulation in vascular endothelium.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>9256479</pmid><doi>10.1073/pnas.94.17.9314</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Antibodies Biochemistry Biological Sciences Cells, Cultured Cellular biology DNA-Binding Proteins - biosynthesis DNA-Binding Proteins - genetics Endothelial cells Endothelium Endothelium, Vascular - physiology Gene Expression Genes Human umbilical vein endothelial cells Humans Identification Immunohistochemistry In Situ Hybridization Molecular Sequence Data Molecules Physiological stimulation Receptors Sequence Alignment Shear stress Signal Transduction - genetics Smad6 Protein Smad7 Protein Stress, Mechanical Trans-Activators |
title | Vascular MADs: Two Novel MAD-Related Genes Selectively Inducible by Flow in Human Vascular Endothelium |
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