The 'ins' and 'outs' of podosomes and invadopodia: characteristics, formation and function
Key Points Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane. They act as sites of attachment to — and degradation of — the extracellular matrix. These structures contain actin regulators such as cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), adapt...
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description | Key Points
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane. They act as sites of attachment to — and degradation of — the extracellular matrix.
These structures contain actin regulators such as cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), adaptor proteins such as Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and several pericellular proteases.
Podosomes are found in vascular smooth muscle and endothelial cells, as well as in cells derived from monocyte lineages. Their presence correlates with migratory ability.
Invadopodia are found in invasive human cancer cells. In two-dimensional culture, their presence correlates with invasive behaviour. However, in three-dimensional culture and
in vivo
, invadopodium-associated proteins are also required for cell growth.
Podosome-associated proteins have been implicated in human developmental and immune disorders, and dysregulation of podosome formation is associated with atherosclerosis.
Small-molecule regulation of podosomes and invadopodia might represent a new therapeutic strategy to treat several diseases.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. Progress has been made in our understanding of the regulation and function of these structures, and their role in human disease.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. The key proteins in these structures include the actin regulators cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), the adaptor proteins Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and the metalloprotease membrane type 1 matrix metalloprotease (MT1MMP; also known as MMP14). Many cell types can produce these structures, including invasive cancer cells, vascular smooth muscle and endothelial cells, and immune cells such as macrophages and dendritic cells. Recently, progress has been made in our understanding of the regulatory and functional aspects of podosome and invadopodium biology and their role in human disease. |
doi_str_mv | 10.1038/nrm3141 |
format | Article |
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Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane. They act as sites of attachment to — and degradation of — the extracellular matrix.
These structures contain actin regulators such as cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), adaptor proteins such as Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and several pericellular proteases.
Podosomes are found in vascular smooth muscle and endothelial cells, as well as in cells derived from monocyte lineages. Their presence correlates with migratory ability.
Invadopodia are found in invasive human cancer cells. In two-dimensional culture, their presence correlates with invasive behaviour. However, in three-dimensional culture and
in vivo
, invadopodium-associated proteins are also required for cell growth.
Podosome-associated proteins have been implicated in human developmental and immune disorders, and dysregulation of podosome formation is associated with atherosclerosis.
Small-molecule regulation of podosomes and invadopodia might represent a new therapeutic strategy to treat several diseases.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. Progress has been made in our understanding of the regulation and function of these structures, and their role in human disease.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. The key proteins in these structures include the actin regulators cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), the adaptor proteins Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and the metalloprotease membrane type 1 matrix metalloprotease (MT1MMP; also known as MMP14). Many cell types can produce these structures, including invasive cancer cells, vascular smooth muscle and endothelial cells, and immune cells such as macrophages and dendritic cells. Recently, progress has been made in our understanding of the regulatory and functional aspects of podosome and invadopodium biology and their role in human disease.</description><identifier>ISSN: 1471-0072</identifier><identifier>EISSN: 1471-0080</identifier><identifier>DOI: 10.1038/nrm3141</identifier><identifier>PMID: 21697900</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/80/84/2339 ; 631/80/84/2340 ; 67 ; 79 ; 84 ; Actin ; Actins - metabolism ; Animals ; Biochemistry ; Biomedical and Life Sciences ; Cancer ; Cancer Research ; Cell Biology ; Cell Movement - physiology ; Cell Surface Extensions - metabolism ; Cell Surface Extensions - physiology ; Cell Surface Extensions - ultrastructure ; Cortactin - metabolism ; Dendritic cells ; Developmental Biology ; Extracellular matrix ; Fibroblasts ; Gene expression ; Humans ; Integrins ; Kinases ; Life Sciences ; Membranes ; Microscopy, Immunoelectron ; Neoplasm Invasiveness ; Neoplasms - metabolism ; Neoplasms - pathology ; Phosphorylation ; Physiological aspects ; Proteins ; review-article ; Smooth muscle ; Stem Cells ; Substrates ; Wiskott-Aldrich Syndrome Protein - metabolism</subject><ispartof>Nature reviews. Molecular cell biology, 2011-07, Vol.12 (7), p.413-426</ispartof><rights>Springer Nature Limited 2011</rights><rights>COPYRIGHT 2011 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jul 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c595t-4650ad431cea2d755936928b612ab53a56d722c82fb096a483530b615a0bfbc33</citedby><cites>FETCH-LOGICAL-c595t-4650ad431cea2d755936928b612ab53a56d722c82fb096a483530b615a0bfbc33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nrm3141$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nrm3141$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21697900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murphy, Danielle A.</creatorcontrib><creatorcontrib>Courtneidge, Sara A.</creatorcontrib><title>The 'ins' and 'outs' of podosomes and invadopodia: characteristics, formation and function</title><title>Nature reviews. Molecular cell biology</title><addtitle>Nat Rev Mol Cell Biol</addtitle><addtitle>Nat Rev Mol Cell Biol</addtitle><description>Key Points
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane. They act as sites of attachment to — and degradation of — the extracellular matrix.
These structures contain actin regulators such as cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), adaptor proteins such as Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and several pericellular proteases.
Podosomes are found in vascular smooth muscle and endothelial cells, as well as in cells derived from monocyte lineages. Their presence correlates with migratory ability.
Invadopodia are found in invasive human cancer cells. In two-dimensional culture, their presence correlates with invasive behaviour. However, in three-dimensional culture and
in vivo
, invadopodium-associated proteins are also required for cell growth.
Podosome-associated proteins have been implicated in human developmental and immune disorders, and dysregulation of podosome formation is associated with atherosclerosis.
Small-molecule regulation of podosomes and invadopodia might represent a new therapeutic strategy to treat several diseases.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. Progress has been made in our understanding of the regulation and function of these structures, and their role in human disease.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. The key proteins in these structures include the actin regulators cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), the adaptor proteins Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and the metalloprotease membrane type 1 matrix metalloprotease (MT1MMP; also known as MMP14). Many cell types can produce these structures, including invasive cancer cells, vascular smooth muscle and endothelial cells, and immune cells such as macrophages and dendritic cells. Recently, progress has been made in our understanding of the regulatory and functional aspects of podosome and invadopodium biology and their role in human disease.</description><subject>631/80/84/2339</subject><subject>631/80/84/2340</subject><subject>67</subject><subject>79</subject><subject>84</subject><subject>Actin</subject><subject>Actins - metabolism</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Cell Biology</subject><subject>Cell Movement - physiology</subject><subject>Cell Surface Extensions - metabolism</subject><subject>Cell Surface Extensions - physiology</subject><subject>Cell Surface Extensions - ultrastructure</subject><subject>Cortactin - metabolism</subject><subject>Dendritic cells</subject><subject>Developmental Biology</subject><subject>Extracellular matrix</subject><subject>Fibroblasts</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Integrins</subject><subject>Kinases</subject><subject>Life Sciences</subject><subject>Membranes</subject><subject>Microscopy, Immunoelectron</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - pathology</subject><subject>Phosphorylation</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>review-article</subject><subject>Smooth muscle</subject><subject>Stem Cells</subject><subject>Substrates</subject><subject>Wiskott-Aldrich Syndrome Protein - metabolism</subject><issn>1471-0072</issn><issn>1471-0080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkl1rFDEUhgex2FrFfyCDXqxCt-Zj8jFeCKVoWygIWm-8CWcyyW7KTLImmaL_3mx3Xd0iucjJeZ_zhnM4VfUCo1OMqHzn40hxgx9VR7gReI6QRI93sSCH1dOUbhHCHAv2pDokmLeiReio-n6zNPXM-TSrwff1LEy5hMHWq9CHFEaT7vPO30EfSs7B-1ovIYLOJrqUnU4ntQ1xhOyCv2ft5PX68aw6sDAk83x7H1ffPn28Ob-cX3--uDo_u55r1rI8bzhD0DcUawOkF4y1lLdEdhwT6BgFxntBiJbEdqjl0EjKKCoqA9TZTlN6XH3Y-K6mbjS9Nj5HGNQquhHiLxXAqX3Fu6VahDtFG0JbJovBbGsQw4_JpKxGl7QZBvAmTElJQQVqqOCFfPWAvA1T9KU7JSVmDeKIFej1BlrAYJTzNpRf9dpSnRGOMJVtiwt1-h-qnN6MTgdvrCv5vYK3ewWFyeZnXsCUkrr6-mWf3XakY0gpGrubBkZqvTBquzCFfPnv8Hbcnw0pwJsNkIrkFyb-bfmh128KtsXx</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Murphy, Danielle A.</creator><creator>Courtneidge, Sara A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110701</creationdate><title>The 'ins' and 'outs' of podosomes and invadopodia: characteristics, formation and function</title><author>Murphy, Danielle A. ; Courtneidge, Sara A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c595t-4650ad431cea2d755936928b612ab53a56d722c82fb096a483530b615a0bfbc33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>631/80/84/2339</topic><topic>631/80/84/2340</topic><topic>67</topic><topic>79</topic><topic>84</topic><topic>Actin</topic><topic>Actins - metabolism</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Cancer</topic><topic>Cancer Research</topic><topic>Cell Biology</topic><topic>Cell Movement - physiology</topic><topic>Cell Surface Extensions - metabolism</topic><topic>Cell Surface Extensions - physiology</topic><topic>Cell Surface Extensions - ultrastructure</topic><topic>Cortactin - metabolism</topic><topic>Dendritic cells</topic><topic>Developmental Biology</topic><topic>Extracellular matrix</topic><topic>Fibroblasts</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Integrins</topic><topic>Kinases</topic><topic>Life Sciences</topic><topic>Membranes</topic><topic>Microscopy, Immunoelectron</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - pathology</topic><topic>Phosphorylation</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>review-article</topic><topic>Smooth muscle</topic><topic>Stem Cells</topic><topic>Substrates</topic><topic>Wiskott-Aldrich Syndrome Protein - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murphy, Danielle A.</creatorcontrib><creatorcontrib>Courtneidge, Sara A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature reviews. Molecular cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murphy, Danielle A.</au><au>Courtneidge, Sara A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The 'ins' and 'outs' of podosomes and invadopodia: characteristics, formation and function</atitle><jtitle>Nature reviews. Molecular cell biology</jtitle><stitle>Nat Rev Mol Cell Biol</stitle><addtitle>Nat Rev Mol Cell Biol</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>12</volume><issue>7</issue><spage>413</spage><epage>426</epage><pages>413-426</pages><issn>1471-0072</issn><eissn>1471-0080</eissn><abstract>Key Points
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane. They act as sites of attachment to — and degradation of — the extracellular matrix.
These structures contain actin regulators such as cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), adaptor proteins such as Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and several pericellular proteases.
Podosomes are found in vascular smooth muscle and endothelial cells, as well as in cells derived from monocyte lineages. Their presence correlates with migratory ability.
Invadopodia are found in invasive human cancer cells. In two-dimensional culture, their presence correlates with invasive behaviour. However, in three-dimensional culture and
in vivo
, invadopodium-associated proteins are also required for cell growth.
Podosome-associated proteins have been implicated in human developmental and immune disorders, and dysregulation of podosome formation is associated with atherosclerosis.
Small-molecule regulation of podosomes and invadopodia might represent a new therapeutic strategy to treat several diseases.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. Progress has been made in our understanding of the regulation and function of these structures, and their role in human disease.
Podosomes and invadopodia are actin-based dynamic protrusions of the plasma membrane of metazoan cells that represent sites of attachment to — and degradation of — the extracellular matrix. The key proteins in these structures include the actin regulators cortactin and neural Wiskott–Aldrich syndrome protein (N-WASP), the adaptor proteins Tyr kinase substrate with four SH3 domains (TKS4) and Tyr kinase substrate with five SH3 domains (TKS5), and the metalloprotease membrane type 1 matrix metalloprotease (MT1MMP; also known as MMP14). Many cell types can produce these structures, including invasive cancer cells, vascular smooth muscle and endothelial cells, and immune cells such as macrophages and dendritic cells. Recently, progress has been made in our understanding of the regulatory and functional aspects of podosome and invadopodium biology and their role in human disease.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>21697900</pmid><doi>10.1038/nrm3141</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/80/84/2339 631/80/84/2340 67 79 84 Actin Actins - metabolism Animals Biochemistry Biomedical and Life Sciences Cancer Cancer Research Cell Biology Cell Movement - physiology Cell Surface Extensions - metabolism Cell Surface Extensions - physiology Cell Surface Extensions - ultrastructure Cortactin - metabolism Dendritic cells Developmental Biology Extracellular matrix Fibroblasts Gene expression Humans Integrins Kinases Life Sciences Membranes Microscopy, Immunoelectron Neoplasm Invasiveness Neoplasms - metabolism Neoplasms - pathology Phosphorylation Physiological aspects Proteins review-article Smooth muscle Stem Cells Substrates Wiskott-Aldrich Syndrome Protein - metabolism |
title | The 'ins' and 'outs' of podosomes and invadopodia: characteristics, formation and function |
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