Fusion between phagosomes, early and late endosomes: a role for actin in fusion between late, but not early endocytic organelles
Actin is implicated in membrane fusion, but the precise mechanisms remain unclear. We showed earlier that membrane organelles catalyze the de novo assembly of F-actin that then facilitates the fusion between latex bead phagosomes and a mixture of early and late endocytic organelles. Here, we correla...
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Veröffentlicht in: | Molecular biology of the cell 2004-01, Vol.15 (1), p.345-358 |
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creator | Kjeken, Rune Egeberg, Morten Habermann, Anja Kuehnel, Mark Peyron, Pascale Floetenmeyer, Matthias Walther, Paul Jahraus, Andrea Defacque, Hélène Kuznetsov, Sergei A Griffiths, Gareth |
description | Actin is implicated in membrane fusion, but the precise mechanisms remain unclear. We showed earlier that membrane organelles catalyze the de novo assembly of F-actin that then facilitates the fusion between latex bead phagosomes and a mixture of early and late endocytic organelles. Here, we correlated the polymerization and organization of F-actin with phagosome and endocytic organelle fusion processes in vitro by using biochemistry and light and electron microscopy. When membrane organelles and cytosol were incubated at 37 degrees C with ATP, cytosolic actin polymerized rapidly and became organized into bundles and networks adjacent to membrane organelles. By 30-min incubation, a gel-like state was formed with little further polymerization of actin thereafter. Also during this time, the bulk of in vitro fusion events occurred between phagosomes/endocytic organelles. The fusion between latex bead phagosomes and late endocytic organelles, or between late endocytic organelles themselves was facilitated by actin, but we failed to detect any effect of perturbing F-actin polymerization on early endosome fusion. Consistent with this, late endosomes, like phagosomes, could nucleate F-actin, whereas early endosomes could not. We propose that actin assembled by phagosomes or late endocytic organelles can provide tracks for fusion-partner organelles to move vectorially toward them, via membrane-bound myosins, to facilitate fusion. |
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We showed earlier that membrane organelles catalyze the de novo assembly of F-actin that then facilitates the fusion between latex bead phagosomes and a mixture of early and late endocytic organelles. Here, we correlated the polymerization and organization of F-actin with phagosome and endocytic organelle fusion processes in vitro by using biochemistry and light and electron microscopy. When membrane organelles and cytosol were incubated at 37 degrees C with ATP, cytosolic actin polymerized rapidly and became organized into bundles and networks adjacent to membrane organelles. By 30-min incubation, a gel-like state was formed with little further polymerization of actin thereafter. Also during this time, the bulk of in vitro fusion events occurred between phagosomes/endocytic organelles. The fusion between latex bead phagosomes and late endocytic organelles, or between late endocytic organelles themselves was facilitated by actin, but we failed to detect any effect of perturbing F-actin polymerization on early endosome fusion. Consistent with this, late endosomes, like phagosomes, could nucleate F-actin, whereas early endosomes could not. We propose that actin assembled by phagosomes or late endocytic organelles can provide tracks for fusion-partner organelles to move vectorially toward them, via membrane-bound myosins, to facilitate fusion.</description><identifier>ISSN: 1059-1524</identifier><identifier>EISSN: 1939-4586</identifier><identifier>DOI: 10.1091/mbc.E03-05-0334</identifier><identifier>PMID: 14617814</identifier><language>eng</language><publisher>United States: The American Society for Cell Biology</publisher><subject>Actins - metabolism ; Adenosine Triphosphate ; Animals ; Cells, Cultured ; Cryoelectron Microscopy ; Cytoskeleton - metabolism ; Cytosol - metabolism ; Endocytosis - physiology ; Endosomes - metabolism ; Macrophages - metabolism ; Membrane Fusion - physiology ; Mice ; Microscopy, Confocal ; Models, Molecular ; Organelles - metabolism ; Phagosomes - metabolism ; Thymosin - metabolism</subject><ispartof>Molecular biology of the cell, 2004-01, Vol.15 (1), p.345-358</ispartof><rights>Copyright © 2004, The American Society for Cell Biology 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-c5ab2319df6a6931fabedb3462556509d15dd54b80d1688fb3b39e1c4109a41a3</citedby><cites>FETCH-LOGICAL-c464t-c5ab2319df6a6931fabedb3462556509d15dd54b80d1688fb3b39e1c4109a41a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC307552/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC307552/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14617814$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kjeken, Rune</creatorcontrib><creatorcontrib>Egeberg, Morten</creatorcontrib><creatorcontrib>Habermann, Anja</creatorcontrib><creatorcontrib>Kuehnel, Mark</creatorcontrib><creatorcontrib>Peyron, Pascale</creatorcontrib><creatorcontrib>Floetenmeyer, Matthias</creatorcontrib><creatorcontrib>Walther, Paul</creatorcontrib><creatorcontrib>Jahraus, Andrea</creatorcontrib><creatorcontrib>Defacque, Hélène</creatorcontrib><creatorcontrib>Kuznetsov, Sergei A</creatorcontrib><creatorcontrib>Griffiths, Gareth</creatorcontrib><title>Fusion between phagosomes, early and late endosomes: a role for actin in fusion between late, but not early endocytic organelles</title><title>Molecular biology of the cell</title><addtitle>Mol Biol Cell</addtitle><description>Actin is implicated in membrane fusion, but the precise mechanisms remain unclear. We showed earlier that membrane organelles catalyze the de novo assembly of F-actin that then facilitates the fusion between latex bead phagosomes and a mixture of early and late endocytic organelles. Here, we correlated the polymerization and organization of F-actin with phagosome and endocytic organelle fusion processes in vitro by using biochemistry and light and electron microscopy. When membrane organelles and cytosol were incubated at 37 degrees C with ATP, cytosolic actin polymerized rapidly and became organized into bundles and networks adjacent to membrane organelles. By 30-min incubation, a gel-like state was formed with little further polymerization of actin thereafter. Also during this time, the bulk of in vitro fusion events occurred between phagosomes/endocytic organelles. The fusion between latex bead phagosomes and late endocytic organelles, or between late endocytic organelles themselves was facilitated by actin, but we failed to detect any effect of perturbing F-actin polymerization on early endosome fusion. Consistent with this, late endosomes, like phagosomes, could nucleate F-actin, whereas early endosomes could not. We propose that actin assembled by phagosomes or late endocytic organelles can provide tracks for fusion-partner organelles to move vectorially toward them, via membrane-bound myosins, to facilitate fusion.</description><subject>Actins - metabolism</subject><subject>Adenosine Triphosphate</subject><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Cryoelectron Microscopy</subject><subject>Cytoskeleton - metabolism</subject><subject>Cytosol - metabolism</subject><subject>Endocytosis - physiology</subject><subject>Endosomes - metabolism</subject><subject>Macrophages - metabolism</subject><subject>Membrane Fusion - physiology</subject><subject>Mice</subject><subject>Microscopy, Confocal</subject><subject>Models, Molecular</subject><subject>Organelles - metabolism</subject><subject>Phagosomes - metabolism</subject><subject>Thymosin - metabolism</subject><issn>1059-1524</issn><issn>1939-4586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1rFEEQbcRgYvTsTfrkKZN0bX_stOAhhESFQC56bvqjZjMy07129yh7y0-3l13UQEEV1HuvPh4h74BdAtNwNTt_ect4x2THOBcvyBlorjshe_Wy1UzqDuRKnJLXpfxgDIRQ61fkFISCdQ_ijDzdLWVMkTqsvxEj3T7aTSppxnJB0eZpR20MdLIVKcZw6HykluY0IR1SptbXMdIWw3OhPeWCuqXSmOpRaq_gd3X0NOWNjThNWN6Qk8FOBd8e8zn5fnf77eZLd__w-evN9X3nhRK189K6FQcdBmWV5jBYh8FxoVZSKsl0ABmCFK5nAVTfD447rhG8aG-yAiw_J58OutvFzRg8xprtZLZ5nG3emWRH87wTx0ezSb8MZ2spV43_4cjP6eeCpZp5LL6d0O5ISzE9Y2stgDfg1QHocyol4_B3BjCzN8000wwybpg0e9Ma4_3_q_3DH13ifwBr5JZ4</recordid><startdate>200401</startdate><enddate>200401</enddate><creator>Kjeken, Rune</creator><creator>Egeberg, Morten</creator><creator>Habermann, Anja</creator><creator>Kuehnel, Mark</creator><creator>Peyron, Pascale</creator><creator>Floetenmeyer, Matthias</creator><creator>Walther, Paul</creator><creator>Jahraus, Andrea</creator><creator>Defacque, Hélène</creator><creator>Kuznetsov, Sergei A</creator><creator>Griffiths, Gareth</creator><general>The American Society for Cell Biology</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>200401</creationdate><title>Fusion between phagosomes, early and late endosomes: a role for actin in fusion between late, but not early endocytic organelles</title><author>Kjeken, Rune ; Egeberg, Morten ; Habermann, Anja ; Kuehnel, Mark ; Peyron, Pascale ; Floetenmeyer, Matthias ; Walther, Paul ; Jahraus, Andrea ; Defacque, Hélène ; Kuznetsov, Sergei A ; Griffiths, Gareth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-c5ab2319df6a6931fabedb3462556509d15dd54b80d1688fb3b39e1c4109a41a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Actins - metabolism</topic><topic>Adenosine Triphosphate</topic><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Cryoelectron Microscopy</topic><topic>Cytoskeleton - metabolism</topic><topic>Cytosol - metabolism</topic><topic>Endocytosis - physiology</topic><topic>Endosomes - metabolism</topic><topic>Macrophages - metabolism</topic><topic>Membrane Fusion - physiology</topic><topic>Mice</topic><topic>Microscopy, Confocal</topic><topic>Models, Molecular</topic><topic>Organelles - metabolism</topic><topic>Phagosomes - metabolism</topic><topic>Thymosin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kjeken, Rune</creatorcontrib><creatorcontrib>Egeberg, Morten</creatorcontrib><creatorcontrib>Habermann, Anja</creatorcontrib><creatorcontrib>Kuehnel, Mark</creatorcontrib><creatorcontrib>Peyron, Pascale</creatorcontrib><creatorcontrib>Floetenmeyer, Matthias</creatorcontrib><creatorcontrib>Walther, Paul</creatorcontrib><creatorcontrib>Jahraus, Andrea</creatorcontrib><creatorcontrib>Defacque, Hélène</creatorcontrib><creatorcontrib>Kuznetsov, Sergei A</creatorcontrib><creatorcontrib>Griffiths, Gareth</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>Molecular biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kjeken, Rune</au><au>Egeberg, Morten</au><au>Habermann, Anja</au><au>Kuehnel, Mark</au><au>Peyron, Pascale</au><au>Floetenmeyer, Matthias</au><au>Walther, Paul</au><au>Jahraus, Andrea</au><au>Defacque, Hélène</au><au>Kuznetsov, Sergei A</au><au>Griffiths, Gareth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fusion between phagosomes, early and late endosomes: a role for actin in fusion between late, but not early endocytic organelles</atitle><jtitle>Molecular biology of the cell</jtitle><addtitle>Mol Biol Cell</addtitle><date>2004-01</date><risdate>2004</risdate><volume>15</volume><issue>1</issue><spage>345</spage><epage>358</epage><pages>345-358</pages><issn>1059-1524</issn><eissn>1939-4586</eissn><abstract>Actin is implicated in membrane fusion, but the precise mechanisms remain unclear. We showed earlier that membrane organelles catalyze the de novo assembly of F-actin that then facilitates the fusion between latex bead phagosomes and a mixture of early and late endocytic organelles. Here, we correlated the polymerization and organization of F-actin with phagosome and endocytic organelle fusion processes in vitro by using biochemistry and light and electron microscopy. When membrane organelles and cytosol were incubated at 37 degrees C with ATP, cytosolic actin polymerized rapidly and became organized into bundles and networks adjacent to membrane organelles. By 30-min incubation, a gel-like state was formed with little further polymerization of actin thereafter. Also during this time, the bulk of in vitro fusion events occurred between phagosomes/endocytic organelles. 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subjects | Actins - metabolism Adenosine Triphosphate Animals Cells, Cultured Cryoelectron Microscopy Cytoskeleton - metabolism Cytosol - metabolism Endocytosis - physiology Endosomes - metabolism Macrophages - metabolism Membrane Fusion - physiology Mice Microscopy, Confocal Models, Molecular Organelles - metabolism Phagosomes - metabolism Thymosin - metabolism |
title | Fusion between phagosomes, early and late endosomes: a role for actin in fusion between late, but not early endocytic organelles |
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