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3D Tissue-Like Assemblies: A Novel Approach to Investigate Virus-Cell Interactions

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3D Tissue-Like Assemblies: A Novel Approach to Investigate Virus-Cell Interactions

Auteurs : Thomas J. Goodwin ; Maureen Mccarthy ; Randall J. Cohrs ; Benedikt B. Kaufer [Allemagne]

Source :

Methods (San Diego, Calif.) [ 1046-2023 ] ; 2015.

RBID : PMC:5489059

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)

Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489059

DOI: 10.1016/j.ymeth.2015.05.010
PubMed: 25986169
PubMed Central: 5489059

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Thomas J. Goodwin

<affiliation><nlm:aff id="A1">Disease Modelling/Tissue Analogues Laboratory, NASA Johnson Space Center; Houston, Texas USA</nlm:aff>
<wicri:noCountry code="subfield">Texas USA</wicri:noCountry>
</affiliation>

Maureen Mccarthy

<affiliation><nlm:aff id="A1">Disease Modelling/Tissue Analogues Laboratory, NASA Johnson Space Center; Houston, Texas USA</nlm:aff>
<wicri:noCountry code="subfield">Texas USA</wicri:noCountry>
</affiliation>

Randall J. Cohrs

<affiliation><nlm:aff id="A2">Departments of Neurology and Microbiology, University of Colorado School of Medicine, Aurora, Colorado USA</nlm:aff>
<wicri:noCountry code="subfield">Colorado USA</wicri:noCountry>
</affiliation>

Le document en format XML

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<front><div type="abstract" xml:lang="en"><p id="P2">Virus-host cell interactions are most commonly analyzed in cells maintained <italic>in vitro</italic>
 as two-dimensional tissue cultures. However, these <italic>in vitro</italic>
 conditions vary quite drastically from the tissues that are commonly infected <italic>in vivo</italic>
. 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 <italic>in vivo</italic>
 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)</p>
</div>
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  <pmc-dir>properties manuscript</pmc-dir>
  <front><journal-meta><journal-id journal-id-type="nlm-journal-id">9426302</journal-id>
<journal-id journal-id-type="pubmed-jr-id">20385</journal-id>
<journal-id journal-id-type="nlm-ta">Methods</journal-id>
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<article-id pub-id-type="manuscript">NIHMS691672</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>3D Tissue-Like Assemblies: A Novel Approach to Investigate Virus-Cell Interactions</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Goodwin</surname>
<given-names>Thomas J.</given-names>
</name>
<xref ref-type="aff" rid="A1">1</xref>
<xref rid="FN1" ref-type="author-notes">*</xref>
</contrib>
<contrib contrib-type="author"><name><surname>McCarthy</surname>
<given-names>Maureen</given-names>
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<xref ref-type="aff" rid="A1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Cohrs</surname>
<given-names>Randall J.</given-names>
</name>
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<xref rid="FN1" ref-type="author-notes">*</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Kaufer</surname>
<given-names>Benedikt B.</given-names>
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<xref rid="FN1" ref-type="author-notes">*</xref>
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<aff id="A1"><label>1</label>
Disease Modelling/Tissue Analogues Laboratory, NASA Johnson Space Center; Houston, Texas USA</aff>
<aff id="A2"><label>2</label>
Departments of Neurology and Microbiology, University of Colorado School of Medicine, Aurora, Colorado USA</aff>
<aff id="A3"><label>3</label>
Institut für Virologie, Freie Universität Berlin, Berlin, Germany</aff>
<author-notes><corresp id="FN1"><label>*</label>
Corresponding authors: Thomas J. Goodwin, <sup>1</sup>
Disease Modeling/Tissue Analogues Laboratory NASA Johnson Space Center, 2101 NASA Parkway, Mailcode: SK, Houston Texas 77058, USA <email>thomas.j.goodwin@nasa.gov</email>
. Randall J. Cohrs, Departments of Neurology and Microbiology, University of Colorado School of Medicine, 12700 E. 19th Avenue, Box B182, Aurora, CO 80045, USA <email>Randall.Cohrs@ucdenver.edu</email>
. Benedikt Kaufer, Institut für Virologie, Freie Universität Berlin, Robert von Ostertag-Straße 7-13, 14163 Berlin, Germany. <email>b.kaufer@fu-berlin.de</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted"><day>22</day>
<month>4</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub"><day>15</day>
<month>5</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="ppub"><day>15</day>
<month>11</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>28</day>
<month>6</month>
<year>2017</year>
</pub-date>
<volume>90</volume>
<fpage>76</fpage>
<lpage>84</lpage>
<pmc-comment>elocation-id from pubmed: 10.1016/j.ymeth.2015.05.010</pmc-comment>
      <abstract><p id="P2">Virus-host cell interactions are most commonly analyzed in cells maintained <italic>in vitro</italic>
 as two-dimensional tissue cultures. However, these <italic>in vitro</italic>
 conditions vary quite drastically from the tissues that are commonly infected <italic>in vivo</italic>
. 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 <italic>in vivo</italic>
 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)</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>

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3D Tissue-Like Assemblies: A Novel Approach to Investigate Virus-Cell Interactions

3D Tissue-Like Assemblies: A Novel Approach to Investigate Virus-Cell Interactions

Source :

Abstract

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Curation

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