The activation of aggresomal pathway in Coxsackievirus B3 infection

Aggresomin muodostuminen on yksi solun puolustusmekanismeista, joka pyrkii estämään proteiinien haitallisen aggregoitumisen solulimassa. Aikaisemmat kokeet ovat näyttäneet, että ihmisen enterovirus-infektio aiheuttaa muutoksia vimentiinissä, tyypin III välikokoisessa filamentissa (Turkki et al., jul...

Full description

Bibliographic Details
Main Author: Matilainen, Johanna
Other Authors: Matemaattis-luonnontieteellinen tiedekunta, Faculty of Sciences, Bio- ja ympäristötieteiden laitos, Department of Biological and Environmental Science, University of Jyväskylä, Jyväskylän yliopisto
Format: Master's thesis
Language:eng
Published: 2016
Subjects:
Online Access: https://jyx.jyu.fi/handle/123456789/51364
_version_ 1828193107016941568
author Matilainen, Johanna
author2 Matemaattis-luonnontieteellinen tiedekunta Faculty of Sciences Bio- ja ympäristötieteiden laitos Department of Biological and Environmental Science University of Jyväskylä Jyväskylän yliopisto
author_facet Matilainen, Johanna Matemaattis-luonnontieteellinen tiedekunta Faculty of Sciences Bio- ja ympäristötieteiden laitos Department of Biological and Environmental Science University of Jyväskylä Jyväskylän yliopisto Matilainen, Johanna Matemaattis-luonnontieteellinen tiedekunta Faculty of Sciences Bio- ja ympäristötieteiden laitos Department of Biological and Environmental Science University of Jyväskylä Jyväskylän yliopisto
author_sort Matilainen, Johanna
datasource_str_mv jyx
description Aggresomin muodostuminen on yksi solun puolustusmekanismeista, joka pyrkii estämään proteiinien haitallisen aggregoitumisen solulimassa. Aikaisemmat kokeet ovat näyttäneet, että ihmisen enterovirus-infektio aiheuttaa muutoksia vimentiinissä, tyypin III välikokoisessa filamentissa (Turkki et al., julkaisematon data). Nämä muutokset ovat hyvin samankaltaisia aggresomin muodostumisen aikana tapahtuvien muutoksien kanssa. Tämän tutkimuksen tarkoituksena oli selvittää mahdollisen aggresomin muodostumisreitin aktivoituminen Coxsackievirus B3 (CVB3) -infektiossa, ja hypoteesimme oli, että häkkimäisten vimentiinirakenteiden muodostumisen lisäksi myös muita aggresomin muodostumisreitin aktivoitumiseen yhdistettyjä tapahtumia voidaan havaita CVB3-infektoiduissa soluissa. Lisäksi arvioimme, että aggresomin muodostumisreitin aktivoituminen voi hyödyttää virusinfektiota tai isäntäsolua. Tutkimme työssä näitä aggresomin muodostumiseen liittyviä solumuutoksia infektoiduissa soluissa käyttämällä immunofluoresenssivärjäystekniikoita ja konfokaalimikroskopiaa. Tuloksemme osoittivat, että CVB3-infektio aiheuttaa häkkimäisen vimentiinirakenteen muodostumisen, ja että tämä rakenteellinen muutos vaatii mikrotubuluksia. Infektio aiheuttaa lisäksi suuria rakenteellisia muutoksia solulimakalvostoon ja Golgin laitteeseen, sekä ubikitiinin ja lämpöshokki (Hsp) 70 proteiinin siirtymisen perinukleaariseen tilaan. Tuloksemme viittaavat siihen, että aggresomireitti voi aktivoitua CVB3-infektiossa. Tietojemme mukaan aggresomireitin aktivoitumista ei ole aikaisemmin osoitettu tapahtuvan enterovirusten aiheuttamien infektioiden aikana. Vaikka enteroviruksia on tutkittu kauan, niiden lisääntymiskierron kaikkia eri vaiheita ei tunneta täysin. Tutkimuksemme tulokset tarjoavat uutta tietoa enterovirus-isäntäsolu –vuorovaikutuksista. Aggresome formation is a cellular defence mechanism that is triggered in order to prevent the accumulation of aggregated proteins in the cytoplasm. It has been previously shown that human enterovirus infection causes changes in vimentin, type III intermediate filament protein (Turkki et al., unpublished data), and these structural changes in vimentin resemble the ones induced during aggresome formation. The aim of this study was to investigate the possible activation of aggresomal pathway during Coxsackievirus B3 (CVB3) infection. The hypothesis was that in addition to a vimentin cage, also other factors of the aggresomal pathway might be involved in viral infection, either for the benefit of the virus or host cell. We investigated these cellular changes by using immunofluorescent techniques and confocal microscope imaging. Our results illustrated that CVB3 infection causes a cage-like vimentin, and this rearrangement is dependent on microtubules. In addition, CVB3 infection was shown to induce major structural changes in the ER and Golgi apparatus, accompanied by the translocation of ubiquitin and Heat shock protein (Hsp) 70 to the perinuclear region. These observations indicated that aggresomal pathway could be involved in CVB3 infection. To our best knowledge, the utilization of aggresomal machinery by enteroviruses has not been shown earlier. Despite the fact that enteroviruses have been under research for a long time, there are still areas of the viral lifecycle that are poorly known. Our findings provide more information about enterovirus-host cell –interactions.
first_indexed 2024-09-11T08:52:59Z
format Pro gradu
free_online_boolean 1
fullrecord [{"key": "dc.contributor.advisor", "value": "Turkki, Paula", "language": "", "element": "contributor", "qualifier": "advisor", "schema": "dc"}, {"key": "dc.contributor.advisor", "value": "Marjom\u00e4ki, Varpu", "language": "", "element": "contributor", "qualifier": "advisor", "schema": "dc"}, {"key": "dc.contributor.author", "value": "Matilainen, Johanna", "language": null, "element": "contributor", "qualifier": "author", "schema": "dc"}, {"key": "dc.date.accessioned", "value": "2016-09-14T12:29:08Z", "language": "", "element": "date", "qualifier": "accessioned", "schema": "dc"}, {"key": "dc.date.available", "value": "2016-09-14T12:29:08Z", "language": "", "element": "date", "qualifier": "available", "schema": "dc"}, {"key": "dc.date.issued", "value": "2016", "language": null, "element": "date", "qualifier": "issued", "schema": "dc"}, {"key": "dc.identifier.other", "value": "oai:jykdok.linneanet.fi:1574676", "language": null, "element": "identifier", "qualifier": "other", "schema": "dc"}, {"key": "dc.identifier.uri", "value": "https://jyx.jyu.fi/handle/123456789/51364", "language": "", "element": "identifier", "qualifier": "uri", "schema": "dc"}, {"key": "dc.description.abstract", "value": "Aggresomin muodostuminen on yksi solun puolustusmekanismeista, joka pyrkii est\u00e4m\u00e4\u00e4n proteiinien haitallisen aggregoitumisen solulimassa. Aikaisemmat kokeet ovat n\u00e4ytt\u00e4neet, ett\u00e4 ihmisen enterovirus-infektio aiheuttaa muutoksia vimentiiniss\u00e4, tyypin III v\u00e4likokoisessa filamentissa (Turkki et al., julkaisematon data). N\u00e4m\u00e4 muutokset ovat hyvin samankaltaisia aggresomin muodostumisen aikana tapahtuvien muutoksien kanssa. T\u00e4m\u00e4n tutkimuksen tarkoituksena oli selvitt\u00e4\u00e4 mahdollisen aggresomin muodostumisreitin aktivoituminen Coxsackievirus B3 (CVB3) -infektiossa, ja hypoteesimme oli, ett\u00e4 h\u00e4kkim\u00e4isten vimentiinirakenteiden muodostumisen lis\u00e4ksi my\u00f6s muita aggresomin muodostumisreitin aktivoitumiseen yhdistettyj\u00e4 tapahtumia voidaan havaita CVB3-infektoiduissa soluissa. Lis\u00e4ksi arvioimme, ett\u00e4 aggresomin muodostumisreitin aktivoituminen voi hy\u00f6dytt\u00e4\u00e4 virusinfektiota tai is\u00e4nt\u00e4solua. Tutkimme ty\u00f6ss\u00e4 n\u00e4it\u00e4 aggresomin muodostumiseen liittyvi\u00e4 solumuutoksia infektoiduissa soluissa k\u00e4ytt\u00e4m\u00e4ll\u00e4 immunofluoresenssiv\u00e4rj\u00e4ystekniikoita ja konfokaalimikroskopiaa. Tuloksemme osoittivat, ett\u00e4 CVB3-infektio aiheuttaa h\u00e4kkim\u00e4isen vimentiinirakenteen muodostumisen, ja ett\u00e4 t\u00e4m\u00e4 rakenteellinen muutos vaatii mikrotubuluksia. Infektio aiheuttaa lis\u00e4ksi suuria rakenteellisia muutoksia solulimakalvostoon ja Golgin laitteeseen, sek\u00e4 ubikitiinin ja l\u00e4mp\u00f6shokki (Hsp) 70 proteiinin siirtymisen perinukleaariseen tilaan. Tuloksemme viittaavat siihen, ett\u00e4 aggresomireitti voi aktivoitua CVB3-infektiossa. Tietojemme mukaan aggresomireitin aktivoitumista ei ole aikaisemmin osoitettu tapahtuvan enterovirusten aiheuttamien infektioiden aikana. Vaikka enteroviruksia on tutkittu kauan, niiden lis\u00e4\u00e4ntymiskierron kaikkia eri vaiheita ei tunneta t\u00e4ysin. Tutkimuksemme tulokset tarjoavat uutta tietoa enterovirus-is\u00e4nt\u00e4solu \u2013vuorovaikutuksista.", "language": "fi", "element": "description", "qualifier": "abstract", "schema": "dc"}, {"key": "dc.description.abstract", "value": "Aggresome formation is a cellular defence mechanism that is triggered in order to prevent the accumulation of aggregated proteins in the cytoplasm. It has been previously shown that human enterovirus infection causes changes in vimentin, type III intermediate filament protein (Turkki et al., unpublished data), and these structural changes in vimentin resemble the ones induced during aggresome formation. The aim of this study was to investigate the possible activation of aggresomal pathway during Coxsackievirus B3 (CVB3) infection. The hypothesis was that in addition to a vimentin cage, also other factors of the aggresomal pathway might be involved in viral infection, either for the benefit of the virus or host cell. We investigated these cellular changes by using immunofluorescent techniques and confocal microscope imaging. Our results illustrated that CVB3 infection causes a cage-like vimentin, and this rearrangement is dependent on microtubules. In addition, CVB3 infection was shown to induce major structural changes in the ER and Golgi apparatus, accompanied by the translocation of ubiquitin and Heat shock protein (Hsp) 70 to the perinuclear region. These observations indicated that aggresomal pathway could be involved in CVB3 infection. To our best knowledge, the utilization of aggresomal machinery by enteroviruses has not been shown earlier. Despite the fact that enteroviruses have been under research for a long time, there are still areas of the viral lifecycle that are poorly known. Our findings provide more information about enterovirus-host cell \u2013interactions.", "language": "en", "element": "description", "qualifier": "abstract", "schema": "dc"}, {"key": "dc.description.provenance", "value": "Submitted using Plone Publishing form by Johanna Matilainen (matijoma) on 2016-09-14 12:29:07.627528. Form: Pro gradu -lomake (https://kirjasto.jyu.fi/julkaisut/julkaisulomakkeet/pro-gradu-lomake). JyX data: [jyx_publishing-allowed (fi) =True]", "language": "en", "element": "description", "qualifier": "provenance", "schema": "dc"}, {"key": "dc.description.provenance", "value": "Submitted by jyx lomake-julkaisija (jyx-julkaisija.group@korppi.jyu.fi) on 2016-09-14T12:29:08Z\r\nNo. of bitstreams: 2\r\nURN:NBN:fi:jyu-201609144108.pdf: 2031259 bytes, checksum: 7665e7c8fa8607a05ff6475f78dc41ac (MD5)\r\nlicense.html: 4833 bytes, checksum: 167a46ebcc1bb560cadda3b52f82fefe (MD5)", "language": "en", "element": "description", "qualifier": "provenance", "schema": "dc"}, {"key": "dc.description.provenance", "value": "Made available in DSpace on 2016-09-14T12:29:08Z (GMT). No. of bitstreams: 2\r\nURN:NBN:fi:jyu-201609144108.pdf: 2031259 bytes, checksum: 7665e7c8fa8607a05ff6475f78dc41ac (MD5)\r\nlicense.html: 4833 bytes, checksum: 167a46ebcc1bb560cadda3b52f82fefe (MD5)\r\n Previous issue date: 2016", "language": "en", "element": "description", "qualifier": "provenance", "schema": "dc"}, {"key": "dc.format.extent", "value": "1 verkkoaineisto (50 sivua)", "language": null, "element": "format", "qualifier": "extent", "schema": "dc"}, {"key": "dc.format.mimetype", "value": "application/pdf", "language": null, "element": "format", "qualifier": "mimetype", "schema": "dc"}, {"key": "dc.language.iso", "value": "eng", "language": null, "element": "language", "qualifier": "iso", "schema": "dc"}, {"key": "dc.rights", "value": "In Copyright", "language": "en", "element": "rights", "qualifier": null, "schema": "dc"}, {"key": "dc.subject.other", "value": "aggresomi", "language": null, "element": "subject", "qualifier": "other", "schema": "dc"}, {"key": "dc.subject.other", "value": "vimentiini", "language": null, "element": "subject", "qualifier": "other", "schema": "dc"}, {"key": "dc.subject.other", "value": "Coxsackievirus B3", "language": null, "element": "subject", "qualifier": "other", "schema": "dc"}, {"key": "dc.subject.other", "value": "aggresome", "language": null, "element": "subject", "qualifier": "other", "schema": "dc"}, {"key": "dc.subject.other", "value": "ER stress", "language": null, "element": "subject", "qualifier": "other", "schema": "dc"}, {"key": "dc.subject.other", "value": "vimentin", "language": null, "element": "subject", "qualifier": "other", "schema": "dc"}, {"key": "dc.title", "value": "The activation of aggresomal pathway in Coxsackievirus B3 infection", "language": null, "element": "title", "qualifier": null, "schema": "dc"}, {"key": "dc.type", "value": "master thesis", "language": null, "element": "type", "qualifier": null, "schema": "dc"}, {"key": "dc.identifier.urn", "value": "URN:NBN:fi:jyu-201609144108", "language": null, "element": "identifier", "qualifier": "urn", "schema": "dc"}, {"key": "dc.type.ontasot", "value": "Pro gradu -tutkielma", "language": "fi", "element": "type", "qualifier": "ontasot", "schema": "dc"}, {"key": "dc.type.ontasot", "value": "Master\u2019s thesis", "language": "en", "element": "type", "qualifier": "ontasot", "schema": "dc"}, {"key": "dc.contributor.faculty", "value": "Matemaattis-luonnontieteellinen tiedekunta", "language": "fi", "element": "contributor", "qualifier": "faculty", "schema": "dc"}, {"key": "dc.contributor.faculty", "value": "Faculty of Sciences", "language": "en", "element": "contributor", "qualifier": "faculty", "schema": "dc"}, {"key": "dc.contributor.department", "value": "Bio- ja ymp\u00e4rist\u00f6tieteiden laitos", "language": "fi", "element": "contributor", "qualifier": "department", "schema": "dc"}, {"key": "dc.contributor.department", "value": "Department of Biological and Environmental Science", "language": "en", "element": "contributor", "qualifier": "department", "schema": "dc"}, {"key": "dc.contributor.organization", "value": "University of Jyv\u00e4skyl\u00e4", "language": "en", "element": "contributor", "qualifier": "organization", "schema": "dc"}, {"key": "dc.contributor.organization", "value": "Jyv\u00e4skyl\u00e4n yliopisto", "language": "fi", "element": "contributor", "qualifier": "organization", "schema": "dc"}, {"key": "dc.subject.discipline", "value": "Solu- ja molekyylibiologia", "language": "fi", "element": "subject", "qualifier": "discipline", "schema": "dc"}, {"key": "dc.subject.discipline", "value": "Cell and molecular biology", "language": "en", "element": "subject", "qualifier": "discipline", "schema": "dc"}, {"key": "dc.date.updated", "value": "2016-09-14T12:29:08Z", "language": "", "element": "date", "qualifier": "updated", "schema": "dc"}, {"key": "yvv.contractresearch.funding", "value": "0", "language": "", "element": "contractresearch", "qualifier": "funding", "schema": "yvv"}, {"key": "dc.type.coar", "value": "http://purl.org/coar/resource_type/c_bdcc", "language": null, "element": "type", "qualifier": "coar", "schema": "dc"}, {"key": "dc.rights.accesslevel", "value": "openAccess", "language": "fi", "element": "rights", "qualifier": "accesslevel", "schema": "dc"}, {"key": "dc.type.publication", "value": "masterThesis", "language": null, "element": "type", "qualifier": "publication", "schema": "dc"}, {"key": "dc.subject.oppiainekoodi", "value": "4013", "language": null, "element": "subject", "qualifier": "oppiainekoodi", "schema": "dc"}, {"key": "dc.subject.yso", "value": "enterovirukset", "language": null, "element": "subject", "qualifier": "yso", "schema": "dc"}, {"key": "dc.subject.yso", "value": "is\u00e4nt\u00e4solut", "language": null, "element": "subject", "qualifier": "yso", "schema": "dc"}, {"key": "dc.subject.yso", "value": "puolustusmekanismit (biologia)", "language": null, "element": "subject", "qualifier": "yso", "schema": "dc"}, {"key": "dc.subject.yso", "value": "infektiot", "language": null, "element": "subject", "qualifier": "yso", "schema": "dc"}, {"key": "dc.format.content", "value": "fulltext", "language": null, "element": "format", "qualifier": "content", "schema": "dc"}, {"key": "dc.rights.url", "value": "https://rightsstatements.org/page/InC/1.0/", "language": null, "element": "rights", "qualifier": "url", "schema": "dc"}, {"key": "dc.type.okm", "value": "G2", "language": null, "element": "type", "qualifier": "okm", "schema": "dc"}]
id jyx.123456789_51364
language eng
last_indexed 2025-03-31T20:03:35Z
main_date 2016-01-01T00:00:00Z
main_date_str 2016
online_boolean 1
online_urls_str_mv {"url":"https:\/\/jyx.jyu.fi\/bitstreams\/ab337dad-0e42-4476-aff4-98a1fcb7982b\/download","text":"URN:NBN:fi:jyu-201609144108.pdf","source":"jyx","mediaType":"application\/pdf"}
publishDate 2016
record_format qdc
source_str_mv jyx
spellingShingle Matilainen, Johanna The activation of aggresomal pathway in Coxsackievirus B3 infection aggresomi vimentiini Coxsackievirus B3 aggresome ER stress vimentin Solu- ja molekyylibiologia Cell and molecular biology 4013 enterovirukset isäntäsolut puolustusmekanismit (biologia) infektiot
title The activation of aggresomal pathway in Coxsackievirus B3 infection
title_full The activation of aggresomal pathway in Coxsackievirus B3 infection
title_fullStr The activation of aggresomal pathway in Coxsackievirus B3 infection The activation of aggresomal pathway in Coxsackievirus B3 infection
title_full_unstemmed The activation of aggresomal pathway in Coxsackievirus B3 infection The activation of aggresomal pathway in Coxsackievirus B3 infection
title_short The activation of aggresomal pathway in Coxsackievirus B3 infection
title_sort activation of aggresomal pathway in coxsackievirus b3 infection
title_txtP The activation of aggresomal pathway in Coxsackievirus B3 infection
topic aggresomi vimentiini Coxsackievirus B3 aggresome ER stress vimentin Solu- ja molekyylibiologia Cell and molecular biology 4013 enterovirukset isäntäsolut puolustusmekanismit (biologia) infektiot
topic_facet 4013 Cell and molecular biology Coxsackievirus B3 ER stress Solu- ja molekyylibiologia aggresome aggresomi enterovirukset infektiot isäntäsolut puolustusmekanismit (biologia) vimentiini vimentin
url https://jyx.jyu.fi/handle/123456789/51364 http://www.urn.fi/URN:NBN:fi:jyu-201609144108
work_keys_str_mv AT matilainenjohanna activationofaggresomalpathwayincoxsackievirusb3infection AT matilainenjohanna theactivationofaggresomalpathwayincoxsackievirusb3infection