3D tissue-like assemblies: A novel approach to investigate virus-cell interactions.
Identifieur interne : 000638 ( PubMed/Checkpoint ); précédent : 000637; suivant : 0006393D tissue-like assemblies: A novel approach to investigate virus-cell interactions.
Auteurs : Thomas J. Goodwin [États-Unis] ; Maureen Mccarthy [États-Unis] ; Randall J. Cohrs [États-Unis] ; Benedikt B. Kaufer [Allemagne]Source :
- Methods (San Diego, Calif.) [ 1095-9130 ] ; 2015.
Descripteurs français
- KwdFr :
- Bioréacteurs, Herpesviridae (physiologie), Herpèsvirus humain de type 3 (physiologie), Humains, Interactions hôte-pathogène, Poumon (virologie), Techniques de culture cellulaire, Virus du SRAS (physiologie), Virus parainfluenza humain de type 3 (physiologie), Virus respiratoires syncytiaux (physiologie).
- MESH :
English descriptors
- KwdEn :
- MESH :
- physiology : Herpesviridae, Herpesvirus 3, Human, Parainfluenza Virus 3, Human, Respiratory Syncytial Viruses, SARS Virus.
- virology : Lung.
- Bioreactors, Cell Culture Techniques, Host-Pathogen Interactions, Humans.
Abstract
Virus-host cell interactions are most commonly analyzed in cells maintained in vitro as two-dimensional tissue cultures. However, these in vitro conditions vary quite drastically from the tissues that are commonly infected in vivo. Over the years, a number of systems have been developed that allow the establishment of three-dimensional (3D) tissue structures that have properties similar to their in vivo 3D counterparts. These 3D systems have numerous applications including drug testing, maintenance of large tissue explants, monitoring migration of human lymphocytes in tissues, analysis of human organ tissue development and investigation of virus-host interactions including viral latency. Here, we describe the establishment of tissue-like assemblies for human lung and neuronal tissue that we infected with a variety of viruses including the respiratory pathogens human parainfluenza virus type 3 (PIV3), respiratory syncytial virus (RSV) and SARS corona virus (SARS-CoV) as well as the human neurotropic herpesvirus, varicella-zoster virus (VZV).
DOI: 10.1016/j.ymeth.2015.05.010
PubMed: 25986169
Affiliations:
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pubmed:25986169Le document en format XML
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Cohrs</name><affiliation wicri:level="1"><nlm:affiliation>Departments of Neurology and Microbiology, University of Colorado School of Medicine, Aurora, CO, USA. Electronic address: Randall.Cohrs@ucdenver.edu.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Departments of Neurology and Microbiology, University of Colorado School of Medicine, Aurora, CO</wicri:regionArea><wicri:noRegion>CO</wicri:noRegion></affiliation></author><author><name sortKey="Kaufer, Benedikt B" sort="Kaufer, Benedikt B" uniqKey="Kaufer B" first="Benedikt B" last="Kaufer">Benedikt B. Kaufer</name><affiliation wicri:level="3"><nlm:affiliation>Institut für Virologie, Freie Universität Berlin, Berlin, Germany. Electronic address: b.kaufer@fu-berlin.de.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institut für Virologie, Freie Universität Berlin, Berlin</wicri:regionArea><placeName><region type="land" nuts="3">Berlin</region><settlement type="city">Berlin</settlement></placeName></affiliation></author></analytic><series><title level="j">Methods (San Diego, Calif.)</title><idno type="eISSN">1095-9130</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bioreactors</term><term>Cell Culture Techniques</term><term>Herpesviridae (physiology)</term><term>Herpesvirus 3, Human (physiology)</term><term>Host-Pathogen Interactions</term><term>Humans</term><term>Lung (virology)</term><term>Parainfluenza Virus 3, Human (physiology)</term><term>Respiratory Syncytial Viruses (physiology)</term><term>SARS Virus (physiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Bioréacteurs</term><term>Herpesviridae (physiologie)</term><term>Herpèsvirus humain de type 3 (physiologie)</term><term>Humains</term><term>Interactions hôte-pathogène</term><term>Poumon (virologie)</term><term>Techniques de culture cellulaire</term><term>Virus du SRAS (physiologie)</term><term>Virus parainfluenza humain de type 3 (physiologie)</term><term>Virus respiratoires syncytiaux (physiologie)</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Herpesviridae</term><term>Herpèsvirus humain de type 3</term><term>Virus du SRAS</term><term>Virus parainfluenza humain de type 3</term><term>Virus respiratoires syncytiaux</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Herpesviridae</term><term>Herpesvirus 3, Human</term><term>Parainfluenza Virus 3, Human</term><term>Respiratory Syncytial Viruses</term><term>SARS Virus</term></keywords><keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Poumon</term></keywords><keywords scheme="MESH" qualifier="virology" xml:lang="en"><term>Lung</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Bioreactors</term><term>Cell Culture Techniques</term><term>Host-Pathogen Interactions</term><term>Humans</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Bioréacteurs</term><term>Humains</term><term>Interactions hôte-pathogène</term><term>Techniques de culture cellulaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Virus-host cell interactions are most commonly analyzed in cells maintained in vitro as two-dimensional tissue cultures. However, these in vitro conditions vary quite drastically from the tissues that are commonly infected in vivo. Over the years, a number of systems have been developed that allow the establishment of three-dimensional (3D) tissue structures that have properties similar to their in vivo 3D counterparts. These 3D systems have numerous applications including drug testing, maintenance of large tissue explants, monitoring migration of human lymphocytes in tissues, analysis of human organ tissue development and investigation of virus-host interactions including viral latency. Here, we describe the establishment of tissue-like assemblies for human lung and neuronal tissue that we infected with a variety of viruses including the respiratory pathogens human parainfluenza virus type 3 (PIV3), respiratory syncytial virus (RSV) and SARS corona virus (SARS-CoV) as well as the human neurotropic herpesvirus, varicella-zoster virus (VZV). </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25986169</PMID><DateCompleted><Year>2016</Year><Month>09</Month><Day>15</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1095-9130</ISSN><JournalIssue CitedMedium="Internet"><Volume>90</Volume><PubDate><Year>2015</Year><Month>Nov</Month><Day>15</Day></PubDate></JournalIssue><Title>Methods (San Diego, Calif.)</Title><ISOAbbreviation>Methods</ISOAbbreviation></Journal><ArticleTitle>3D tissue-like assemblies: A novel approach to investigate virus-cell interactions.</ArticleTitle><Pagination><MedlinePgn>76-84</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ymeth.2015.05.010</ELocationID><ELocationID EIdType="pii" ValidYN="Y">S1046-2023(15)00203-0</ELocationID><Abstract><AbstractText>Virus-host cell interactions are most commonly analyzed in cells maintained in vitro as two-dimensional tissue cultures. However, these in vitro conditions vary quite drastically from the tissues that are commonly infected in vivo. Over the years, a number of systems have been developed that allow the establishment of three-dimensional (3D) tissue structures that have properties similar to their in vivo 3D counterparts. These 3D systems have numerous applications including drug testing, maintenance of large tissue explants, monitoring migration of human lymphocytes in tissues, analysis of human organ tissue development and investigation of virus-host interactions including viral latency. Here, we describe the establishment of tissue-like assemblies for human lung and neuronal tissue that we infected with a variety of viruses including the respiratory pathogens human parainfluenza virus type 3 (PIV3), respiratory syncytial virus (RSV) and SARS corona virus (SARS-CoV) as well as the human neurotropic herpesvirus, varicella-zoster virus (VZV). </AbstractText><CopyrightInformation>Copyright © 2015 Elsevier Inc. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Goodwin</LastName><ForeName>Thomas J</ForeName><Initials>TJ</Initials><AffiliationInfo><Affiliation>Disease Modelling/Tissue Analogues Laboratory, NASA Johnson Space Center, Houston, TX, USA. Electronic address: thomas.j.goodwin@nasa.gov.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>McCarthy</LastName><ForeName>Maureen</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Disease Modelling/Tissue Analogues Laboratory, NASA Johnson Space Center, Houston, TX, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cohrs</LastName><ForeName>Randall J</ForeName><Initials>RJ</Initials><AffiliationInfo><Affiliation>Departments of Neurology and Microbiology, University of Colorado School of Medicine, Aurora, CO, USA. Electronic address: Randall.Cohrs@ucdenver.edu.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kaufer</LastName><ForeName>Benedikt B</ForeName><Initials>BB</Initials><AffiliationInfo><Affiliation>Institut für Virologie, Freie Universität Berlin, Berlin, Germany. 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