Desmoplakin is required for microvascular tube formation in culture
Desmoplakin (DP) is a key component of cellular adhesion junctions known as desmosomes; however, recent investigations have revealed a novel location for DP in junctions separate from desmosomes termed complexus adherens junctions. These junctions are found at contact sites between endothelial cells...
Gespeichert in:
Veröffentlicht in: | Journal of cell science 2004-07, Vol.117 (Pt 15), p.3129-3140 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3140 |
---|---|
container_issue | Pt 15 |
container_start_page | 3129 |
container_title | Journal of cell science |
container_volume | 117 |
creator | Zhou, Xuan Stuart, August Dettin, Luis E Rodriguez, Gisela Hoel, Bonnie Gallicano, G Ian |
description | Desmoplakin (DP) is a key component of cellular adhesion junctions known as desmosomes; however, recent investigations have revealed a novel location for DP in junctions separate from desmosomes termed complexus adherens junctions. These junctions are found at contact sites between endothelial cells that line capillaries. Few studies have focused on the function of DP in de novo capillary formation (vasculogenesis) and branching (angiogenesis) during tumorigenesis, embryonic development, cardiovascular development or wound healing. Only recently have investigations begun to determine the effect the loss of DP has on capillaries during embryogenesis (i.e. in DP-/- mice). Evidence shows that the loss of desmoplakin in vivo results in leaky capillaries and/or capillary malformation. Consequently, the goal of this study was to determine the function of DP in complexus adherens junctions during capillary formation. To accomplish this goal, we used siRNA technology to knock down desmoplakin expression in endothelial cells before they were induced to form microvascular tubes on matrigel. DP siRNA treated cells sent out filopodia and came in close contact with each other when plated onto matrigel; however, in most cases they failed to form tubes as compared with control endothelial cells. Interestingly, after siRNA degradation, endothelial cells were then capable of forming microvascular tubes. In depth analyses into the function of DP in capillary formation were not previously possible because the tools and experimental approaches only recently have become available (i.e. siRNA). Consequently, fully understanding the role of desmoplakin in capillary formation may lead to a novel approach for inhibiting vasculo- and angiogenesis in tumor formation. |
doi_str_mv | 10.1242/jcs.01132 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_66659233</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>66659233</sourcerecordid><originalsourceid>FETCH-LOGICAL-c384t-9d21cf9765e1616f2ff8c0b5926ef0df9f917d4beba0beaf969ae3087e4885c13</originalsourceid><addsrcrecordid>eNpFkE1LxDAURYMoTh1d-AekK8FFx7ykTZqljJ8w4EbXJU1fIGM7nUkawX9vxhlw9eBy7uVxCLkGugBWsvu1CQsKwNkJyaCUslDA5SnJKGVQqIrzGbkIYU0plUzJczKDClQqqIwsHzEM47bXX26Tu5B73EXnscvt6PPBGT9-62Bir30-xRb38aAnNyZ4k6d8ih4vyZnVfcCr452Tz-enj-VrsXp_eVs-rArD63IqVMfAWCVFhSBAWGZtbWhbKSbQ0s4qq0B2ZYutpi1qq4TSyGktsazrygCfk9vD7taPu4hhagYXDPa93uAYQyOESGOcJ_DuAKb3Q_Bom613g_Y_DdBmb6xJxpo_Y4m9OY7GdsDunzwq4r8QtGds</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66659233</pqid></control><display><type>article</type><title>Desmoplakin is required for microvascular tube formation in culture</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Company of Biologists</source><creator>Zhou, Xuan ; Stuart, August ; Dettin, Luis E ; Rodriguez, Gisela ; Hoel, Bonnie ; Gallicano, G Ian</creator><creatorcontrib>Zhou, Xuan ; Stuart, August ; Dettin, Luis E ; Rodriguez, Gisela ; Hoel, Bonnie ; Gallicano, G Ian</creatorcontrib><description>Desmoplakin (DP) is a key component of cellular adhesion junctions known as desmosomes; however, recent investigations have revealed a novel location for DP in junctions separate from desmosomes termed complexus adherens junctions. These junctions are found at contact sites between endothelial cells that line capillaries. Few studies have focused on the function of DP in de novo capillary formation (vasculogenesis) and branching (angiogenesis) during tumorigenesis, embryonic development, cardiovascular development or wound healing. Only recently have investigations begun to determine the effect the loss of DP has on capillaries during embryogenesis (i.e. in DP-/- mice). Evidence shows that the loss of desmoplakin in vivo results in leaky capillaries and/or capillary malformation. Consequently, the goal of this study was to determine the function of DP in complexus adherens junctions during capillary formation. To accomplish this goal, we used siRNA technology to knock down desmoplakin expression in endothelial cells before they were induced to form microvascular tubes on matrigel. DP siRNA treated cells sent out filopodia and came in close contact with each other when plated onto matrigel; however, in most cases they failed to form tubes as compared with control endothelial cells. Interestingly, after siRNA degradation, endothelial cells were then capable of forming microvascular tubes. In depth analyses into the function of DP in capillary formation were not previously possible because the tools and experimental approaches only recently have become available (i.e. siRNA). Consequently, fully understanding the role of desmoplakin in capillary formation may lead to a novel approach for inhibiting vasculo- and angiogenesis in tumor formation.</description><identifier>ISSN: 0021-9533</identifier><identifier>EISSN: 1477-9137</identifier><identifier>DOI: 10.1242/jcs.01132</identifier><identifier>PMID: 15190119</identifier><language>eng</language><publisher>England</publisher><subject>Alleles ; Animals ; Antigens, CD ; Blotting, Western ; Cadherins - metabolism ; Capillaries - metabolism ; Cell Adhesion ; Cell Line ; Collagen - pharmacology ; Cytoskeletal Proteins - metabolism ; Cytoskeletal Proteins - physiology ; Desmoplakins ; Desmosomes - metabolism ; Drug Combinations ; Endothelium, Vascular - metabolism ; Green Fluorescent Proteins - metabolism ; Humans ; Immunohistochemistry ; Laminin - pharmacology ; Mice ; Mice, Transgenic ; Microcirculation ; Microscopy, Electron ; Microscopy, Fluorescence ; Neovascularization, Physiologic ; Proteoglycans - pharmacology ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Small Interfering - metabolism ; Time Factors</subject><ispartof>Journal of cell science, 2004-07, Vol.117 (Pt 15), p.3129-3140</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-9d21cf9765e1616f2ff8c0b5926ef0df9f917d4beba0beaf969ae3087e4885c13</citedby><cites>FETCH-LOGICAL-c384t-9d21cf9765e1616f2ff8c0b5926ef0df9f917d4beba0beaf969ae3087e4885c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3664,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15190119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Xuan</creatorcontrib><creatorcontrib>Stuart, August</creatorcontrib><creatorcontrib>Dettin, Luis E</creatorcontrib><creatorcontrib>Rodriguez, Gisela</creatorcontrib><creatorcontrib>Hoel, Bonnie</creatorcontrib><creatorcontrib>Gallicano, G Ian</creatorcontrib><title>Desmoplakin is required for microvascular tube formation in culture</title><title>Journal of cell science</title><addtitle>J Cell Sci</addtitle><description>Desmoplakin (DP) is a key component of cellular adhesion junctions known as desmosomes; however, recent investigations have revealed a novel location for DP in junctions separate from desmosomes termed complexus adherens junctions. These junctions are found at contact sites between endothelial cells that line capillaries. Few studies have focused on the function of DP in de novo capillary formation (vasculogenesis) and branching (angiogenesis) during tumorigenesis, embryonic development, cardiovascular development or wound healing. Only recently have investigations begun to determine the effect the loss of DP has on capillaries during embryogenesis (i.e. in DP-/- mice). Evidence shows that the loss of desmoplakin in vivo results in leaky capillaries and/or capillary malformation. Consequently, the goal of this study was to determine the function of DP in complexus adherens junctions during capillary formation. To accomplish this goal, we used siRNA technology to knock down desmoplakin expression in endothelial cells before they were induced to form microvascular tubes on matrigel. DP siRNA treated cells sent out filopodia and came in close contact with each other when plated onto matrigel; however, in most cases they failed to form tubes as compared with control endothelial cells. Interestingly, after siRNA degradation, endothelial cells were then capable of forming microvascular tubes. In depth analyses into the function of DP in capillary formation were not previously possible because the tools and experimental approaches only recently have become available (i.e. siRNA). Consequently, fully understanding the role of desmoplakin in capillary formation may lead to a novel approach for inhibiting vasculo- and angiogenesis in tumor formation.</description><subject>Alleles</subject><subject>Animals</subject><subject>Antigens, CD</subject><subject>Blotting, Western</subject><subject>Cadherins - metabolism</subject><subject>Capillaries - metabolism</subject><subject>Cell Adhesion</subject><subject>Cell Line</subject><subject>Collagen - pharmacology</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Cytoskeletal Proteins - physiology</subject><subject>Desmoplakins</subject><subject>Desmosomes - metabolism</subject><subject>Drug Combinations</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Laminin - pharmacology</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Microcirculation</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Fluorescence</subject><subject>Neovascularization, Physiologic</subject><subject>Proteoglycans - pharmacology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Small Interfering - metabolism</subject><subject>Time Factors</subject><issn>0021-9533</issn><issn>1477-9137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1LxDAURYMoTh1d-AekK8FFx7ykTZqljJ8w4EbXJU1fIGM7nUkawX9vxhlw9eBy7uVxCLkGugBWsvu1CQsKwNkJyaCUslDA5SnJKGVQqIrzGbkIYU0plUzJczKDClQqqIwsHzEM47bXX26Tu5B73EXnscvt6PPBGT9-62Bir30-xRb38aAnNyZ4k6d8ih4vyZnVfcCr452Tz-enj-VrsXp_eVs-rArD63IqVMfAWCVFhSBAWGZtbWhbKSbQ0s4qq0B2ZYutpi1qq4TSyGktsazrygCfk9vD7taPu4hhagYXDPa93uAYQyOESGOcJ_DuAKb3Q_Bom613g_Y_DdBmb6xJxpo_Y4m9OY7GdsDunzwq4r8QtGds</recordid><startdate>20040701</startdate><enddate>20040701</enddate><creator>Zhou, Xuan</creator><creator>Stuart, August</creator><creator>Dettin, Luis E</creator><creator>Rodriguez, Gisela</creator><creator>Hoel, Bonnie</creator><creator>Gallicano, G Ian</creator><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>20040701</creationdate><title>Desmoplakin is required for microvascular tube formation in culture</title><author>Zhou, Xuan ; Stuart, August ; Dettin, Luis E ; Rodriguez, Gisela ; Hoel, Bonnie ; Gallicano, G Ian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-9d21cf9765e1616f2ff8c0b5926ef0df9f917d4beba0beaf969ae3087e4885c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Alleles</topic><topic>Animals</topic><topic>Antigens, CD</topic><topic>Blotting, Western</topic><topic>Cadherins - metabolism</topic><topic>Capillaries - metabolism</topic><topic>Cell Adhesion</topic><topic>Cell Line</topic><topic>Collagen - pharmacology</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Cytoskeletal Proteins - physiology</topic><topic>Desmoplakins</topic><topic>Desmosomes - metabolism</topic><topic>Drug Combinations</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Laminin - pharmacology</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Microcirculation</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Fluorescence</topic><topic>Neovascularization, Physiologic</topic><topic>Proteoglycans - pharmacology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Small Interfering - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Xuan</creatorcontrib><creatorcontrib>Stuart, August</creatorcontrib><creatorcontrib>Dettin, Luis E</creatorcontrib><creatorcontrib>Rodriguez, Gisela</creatorcontrib><creatorcontrib>Hoel, Bonnie</creatorcontrib><creatorcontrib>Gallicano, G Ian</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>Journal of cell science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Xuan</au><au>Stuart, August</au><au>Dettin, Luis E</au><au>Rodriguez, Gisela</au><au>Hoel, Bonnie</au><au>Gallicano, G Ian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Desmoplakin is required for microvascular tube formation in culture</atitle><jtitle>Journal of cell science</jtitle><addtitle>J Cell Sci</addtitle><date>2004-07-01</date><risdate>2004</risdate><volume>117</volume><issue>Pt 15</issue><spage>3129</spage><epage>3140</epage><pages>3129-3140</pages><issn>0021-9533</issn><eissn>1477-9137</eissn><abstract>Desmoplakin (DP) is a key component of cellular adhesion junctions known as desmosomes; however, recent investigations have revealed a novel location for DP in junctions separate from desmosomes termed complexus adherens junctions. These junctions are found at contact sites between endothelial cells that line capillaries. Few studies have focused on the function of DP in de novo capillary formation (vasculogenesis) and branching (angiogenesis) during tumorigenesis, embryonic development, cardiovascular development or wound healing. Only recently have investigations begun to determine the effect the loss of DP has on capillaries during embryogenesis (i.e. in DP-/- mice). Evidence shows that the loss of desmoplakin in vivo results in leaky capillaries and/or capillary malformation. Consequently, the goal of this study was to determine the function of DP in complexus adherens junctions during capillary formation. To accomplish this goal, we used siRNA technology to knock down desmoplakin expression in endothelial cells before they were induced to form microvascular tubes on matrigel. DP siRNA treated cells sent out filopodia and came in close contact with each other when plated onto matrigel; however, in most cases they failed to form tubes as compared with control endothelial cells. Interestingly, after siRNA degradation, endothelial cells were then capable of forming microvascular tubes. In depth analyses into the function of DP in capillary formation were not previously possible because the tools and experimental approaches only recently have become available (i.e. siRNA). Consequently, fully understanding the role of desmoplakin in capillary formation may lead to a novel approach for inhibiting vasculo- and angiogenesis in tumor formation.</abstract><cop>England</cop><pmid>15190119</pmid><doi>10.1242/jcs.01132</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9533 |
ispartof | Journal of cell science, 2004-07, Vol.117 (Pt 15), p.3129-3140 |
issn | 0021-9533 1477-9137 |
language | eng |
recordid | cdi_proquest_miscellaneous_66659233 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Company of Biologists |
subjects | Alleles Animals Antigens, CD Blotting, Western Cadherins - metabolism Capillaries - metabolism Cell Adhesion Cell Line Collagen - pharmacology Cytoskeletal Proteins - metabolism Cytoskeletal Proteins - physiology Desmoplakins Desmosomes - metabolism Drug Combinations Endothelium, Vascular - metabolism Green Fluorescent Proteins - metabolism Humans Immunohistochemistry Laminin - pharmacology Mice Mice, Transgenic Microcirculation Microscopy, Electron Microscopy, Fluorescence Neovascularization, Physiologic Proteoglycans - pharmacology Reverse Transcriptase Polymerase Chain Reaction RNA, Small Interfering - metabolism Time Factors |
title | Desmoplakin is required for microvascular tube formation in culture |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T00%3A28%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Desmoplakin%20is%20required%20for%20microvascular%20tube%20formation%20in%20culture&rft.jtitle=Journal%20of%20cell%20science&rft.au=Zhou,%20Xuan&rft.date=2004-07-01&rft.volume=117&rft.issue=Pt%2015&rft.spage=3129&rft.epage=3140&rft.pages=3129-3140&rft.issn=0021-9533&rft.eissn=1477-9137&rft_id=info:doi/10.1242/jcs.01132&rft_dat=%3Cproquest_cross%3E66659233%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=66659233&rft_id=info:pmid/15190119&rfr_iscdi=true |