The parasitophorus vacuole membrane surrounding intracellular Toxoplasma gondii functions as a molecular sieve
The obligate intracellular protozoan parasite Toxoplasma gondii creates and enters into a unique membrane-bounded cytoplasmic compartment, the parasitophorous vacuole, when invading mammalian host cells. By microinjecting polar fluorescent molecules into individual T. gondii-infected fibroblasts, we...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1994-01, Vol.91 (2), p.509-513 |
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creator | Schwab, J.C Beckers, C.J.M Joiner, K.A |
description | The obligate intracellular protozoan parasite Toxoplasma gondii creates and enters into a unique membrane-bounded cytoplasmic compartment, the parasitophorous vacuole, when invading mammalian host cells. By microinjecting polar fluorescent molecules into individual T. gondii-infected fibroblasts, we show here that the parasitophorous vacuole membrane (PVM) surrounding the parasite functions as a molecular sieve. Lucifer yellow (457 Da) displayed free bidirectional flux across the PVM and distinctly outlined the parasites, which did not take up the dye, within the vacuole. This dye movement was not appreciably delayed by pretreatment of cells with 5 mM probenecid or chilling the monolayer to 5 degrees C, suggesting that dye movement was due to passive permeation through a membrane pore rather than active transport. Calcein, fluo-3, and a series of fluorescein isothiocyanate-labeled peptides up to 1291 Da crossed the PVM in a size-restricted fashion. A labeled peptide of 1926 Da and labeled dextrans and proteins (greater than or equal to 3000 Da) faded to transit the PVM. This putative channel in the PVM therefore allows exchange of molecules up to 1300-1900 Da between the host cell cytoplasm and the parasitophorous vacuolar space |
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By microinjecting polar fluorescent molecules into individual T. gondii-infected fibroblasts, we show here that the parasitophorous vacuole membrane (PVM) surrounding the parasite functions as a molecular sieve. Lucifer yellow (457 Da) displayed free bidirectional flux across the PVM and distinctly outlined the parasites, which did not take up the dye, within the vacuole. This dye movement was not appreciably delayed by pretreatment of cells with 5 mM probenecid or chilling the monolayer to 5 degrees C, suggesting that dye movement was due to passive permeation through a membrane pore rather than active transport. Calcein, fluo-3, and a series of fluorescein isothiocyanate-labeled peptides up to 1291 Da crossed the PVM in a size-restricted fashion. A labeled peptide of 1926 Da and labeled dextrans and proteins (greater than or equal to 3000 Da) faded to transit the PVM. This putative channel in the PVM therefore allows exchange of molecules up to 1300-1900 Da between the host cell cytoplasm and the parasitophorous vacuolar space</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><language>eng</language><publisher>National Academy of Sciences of the United States of America</publisher><subject>Cell membranes ; COLORANT ; COLORANTES ; Cytoplasm ; DIFFUSION ; DIFUSION ; Dyes ; Fibroblasts ; Fluorescence ; MEMBRANAS CELULARES ; MEMBRANE CELLULAIRE ; Microinjections ; Parasite hosts ; Parasites ; Parasitism ; PEPTIDE ; PEPTIDOS ; TOXOPLASMA GONDII ; VACUOLA ; VACUOLE ; Vacuoles</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1994-01, Vol.91 (2), p.509-513</ispartof><rights>Copyright 1994 The National Academy of Sciences of the United States of America</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2363913$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2363913$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,58017,58250</link.rule.ids></links><search><creatorcontrib>Schwab, J.C</creatorcontrib><creatorcontrib>Beckers, C.J.M</creatorcontrib><creatorcontrib>Joiner, K.A</creatorcontrib><title>The parasitophorus vacuole membrane surrounding intracellular Toxoplasma gondii functions as a molecular sieve</title><title>Proceedings of the National Academy of Sciences - PNAS</title><description>The obligate intracellular protozoan parasite Toxoplasma gondii creates and enters into a unique membrane-bounded cytoplasmic compartment, the parasitophorous vacuole, when invading mammalian host cells. By microinjecting polar fluorescent molecules into individual T. gondii-infected fibroblasts, we show here that the parasitophorous vacuole membrane (PVM) surrounding the parasite functions as a molecular sieve. Lucifer yellow (457 Da) displayed free bidirectional flux across the PVM and distinctly outlined the parasites, which did not take up the dye, within the vacuole. This dye movement was not appreciably delayed by pretreatment of cells with 5 mM probenecid or chilling the monolayer to 5 degrees C, suggesting that dye movement was due to passive permeation through a membrane pore rather than active transport. Calcein, fluo-3, and a series of fluorescein isothiocyanate-labeled peptides up to 1291 Da crossed the PVM in a size-restricted fashion. A labeled peptide of 1926 Da and labeled dextrans and proteins (greater than or equal to 3000 Da) faded to transit the PVM. This putative channel in the PVM therefore allows exchange of molecules up to 1300-1900 Da between the host cell cytoplasm and the parasitophorous vacuolar space</description><subject>Cell membranes</subject><subject>COLORANT</subject><subject>COLORANTES</subject><subject>Cytoplasm</subject><subject>DIFFUSION</subject><subject>DIFUSION</subject><subject>Dyes</subject><subject>Fibroblasts</subject><subject>Fluorescence</subject><subject>MEMBRANAS CELULARES</subject><subject>MEMBRANE CELLULAIRE</subject><subject>Microinjections</subject><subject>Parasite hosts</subject><subject>Parasites</subject><subject>Parasitism</subject><subject>PEPTIDE</subject><subject>PEPTIDOS</subject><subject>TOXOPLASMA GONDII</subject><subject>VACUOLA</subject><subject>VACUOLE</subject><subject>Vacuoles</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNotj8tKxDAYhYMoOI6-gLjICxRy6yVLGbzBgAvruvzNpZOhTUrSDPr2FmfgwFmcjw_OFdpQImlRCUmu0YYQVheNYOIW3aV0JITIsiEb5NuDwTNESG4J8yHEnPAJVA6jwZOZ-gje4JRjDNlr5wfs_BJBmXHMI0Tchp8wj5AmwENYAYdt9mpxwScMa_C0itQ_mpw5mXt0Y2FM5uHSW9S-vrS792L_-faxe94XVhBe9JRZqOqyNFoQRXXZCM01lZqyRtYgmNWMQtWvD6BWVgljG2BGEg2VoVzwLXo6a49pCbGbo5sg_naMV1xSvs6P59lC6GCILnXfX1IIxpnkf08-Xnk</recordid><startdate>19940118</startdate><enddate>19940118</enddate><creator>Schwab, J.C</creator><creator>Beckers, C.J.M</creator><creator>Joiner, K.A</creator><general>National Academy of Sciences of the United States of America</general><scope>FBQ</scope></search><sort><creationdate>19940118</creationdate><title>The parasitophorus vacuole membrane surrounding intracellular Toxoplasma gondii functions as a molecular sieve</title><author>Schwab, J.C ; Beckers, C.J.M ; Joiner, K.A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f403-b12fa6755ed40c1d584d3d19d12897a42fd21a6b580a7cfc4ef8a2e90da6e1343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Cell membranes</topic><topic>COLORANT</topic><topic>COLORANTES</topic><topic>Cytoplasm</topic><topic>DIFFUSION</topic><topic>DIFUSION</topic><topic>Dyes</topic><topic>Fibroblasts</topic><topic>Fluorescence</topic><topic>MEMBRANAS CELULARES</topic><topic>MEMBRANE CELLULAIRE</topic><topic>Microinjections</topic><topic>Parasite hosts</topic><topic>Parasites</topic><topic>Parasitism</topic><topic>PEPTIDE</topic><topic>PEPTIDOS</topic><topic>TOXOPLASMA GONDII</topic><topic>VACUOLA</topic><topic>VACUOLE</topic><topic>Vacuoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwab, J.C</creatorcontrib><creatorcontrib>Beckers, C.J.M</creatorcontrib><creatorcontrib>Joiner, K.A</creatorcontrib><collection>AGRIS</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwab, J.C</au><au>Beckers, C.J.M</au><au>Joiner, K.A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The parasitophorus vacuole membrane surrounding intracellular Toxoplasma gondii functions as a molecular sieve</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><date>1994-01-18</date><risdate>1994</risdate><volume>91</volume><issue>2</issue><spage>509</spage><epage>513</epage><pages>509-513</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The obligate intracellular protozoan parasite Toxoplasma gondii creates and enters into a unique membrane-bounded cytoplasmic compartment, the parasitophorous vacuole, when invading mammalian host cells. By microinjecting polar fluorescent molecules into individual T. gondii-infected fibroblasts, we show here that the parasitophorous vacuole membrane (PVM) surrounding the parasite functions as a molecular sieve. Lucifer yellow (457 Da) displayed free bidirectional flux across the PVM and distinctly outlined the parasites, which did not take up the dye, within the vacuole. This dye movement was not appreciably delayed by pretreatment of cells with 5 mM probenecid or chilling the monolayer to 5 degrees C, suggesting that dye movement was due to passive permeation through a membrane pore rather than active transport. Calcein, fluo-3, and a series of fluorescein isothiocyanate-labeled peptides up to 1291 Da crossed the PVM in a size-restricted fashion. A labeled peptide of 1926 Da and labeled dextrans and proteins (greater than or equal to 3000 Da) faded to transit the PVM. This putative channel in the PVM therefore allows exchange of molecules up to 1300-1900 Da between the host cell cytoplasm and the parasitophorous vacuolar space</abstract><pub>National Academy of Sciences of the United States of America</pub><tpages>5</tpages></addata></record> |
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source | JSTOR Archive Collection A-Z Listing; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Cell membranes COLORANT COLORANTES Cytoplasm DIFFUSION DIFUSION Dyes Fibroblasts Fluorescence MEMBRANAS CELULARES MEMBRANE CELLULAIRE Microinjections Parasite hosts Parasites Parasitism PEPTIDE PEPTIDOS TOXOPLASMA GONDII VACUOLA VACUOLE Vacuoles |
title | The parasitophorus vacuole membrane surrounding intracellular Toxoplasma gondii functions as a molecular sieve |
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