Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26829
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dc.contributor.authorCollett, Simon-
dc.contributor.authorTorresi, Joseph-
dc.contributor.authorSilveira, Linda Earnest-
dc.contributor.authorTruong, Vi Khanh-
dc.contributor.authorChristiansen, Dale-
dc.contributor.authorTran, Bang M-
dc.contributor.authorVincan, Elizabeth-
dc.contributor.authorRamsland, Paul A-
dc.contributor.authorElbourne, Aaron-
dc.date2021-02-23-
dc.date.accessioned2021-06-28T06:12:24Z-
dc.date.available2021-06-28T06:12:24Z-
dc.date.issued2021-06-15-
dc.identifier.citationJournal of Colloid and Interface Science 2021; 592: 371-384en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26829-
dc.description.abstractCell cultures have been successfully used to study hepatitis C virus (HCV) for many years. However, most work has been done using traditional, 2-dimensional (2D) cell cultures (cells grown as a monolayer in growth flasks or dishes). Studies have shown that when cells are grown suspended in an extra-cellular-matrix-like material, they develop into spherical, 'organoid' arrangements of cells (3D growth) that display distinct differences in morphological and functional characteristics compared to 2D cell cultures. In liver organoids, one key difference is the development of clearly differentiated apical and basolateral surfaces separated and maintained by cellular tight junctions. This phenomenon, termed polarity, is vital to normal barrier function of hepatocytes in vivo. It has also been shown that viruses, and virus-like particles, interact very differently with cells derived from 2D as compared to 3D cell cultures, bringing into question the usefulness of 2D cell cultures to study virus-host cell interactions. Here, we investigate differences in cellular architecture as a function of cell culture system, using confocal scanning laser microscopy, and determine differences in binding interactions between HCV virus-like particles (VLPs) and their cognate receptors in the different cell culture systems using atomic force microscopy (AFM). We generated organoid cultures that were polarized, as determined by localization of key apical and basolateral markers. We found that, while uptake of HCV VLPs by both 2D and 3D Huh7 cells was observed by flow cytometry, binding interactions between HCV VLPs and cells were measurable by AFM only on polarized cells. The work presented here adds to the growing body of research suggesting that polarized cell systems are more suitable for the study of HCV infection and dynamics than non-polarized systems.en
dc.language.isoeng
dc.subjectAtomic force microscopyen
dc.subjectBio-interfaceen
dc.subjectEnveloped virus-like particlesen
dc.subjectNanostructureen
dc.subjectVaccine developmenten
dc.titleInvestigating virus-host cell interactions: Comparative binding forces between hepatitis C virus-like particles and host cell receptors in 2D and 3D cell culture models.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Colloid and Interface Scienceen
dc.identifier.affiliationDepartment of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, VIC 3010, Australiaen
dc.identifier.affiliationDepartment of Immunology, Monash University, Melbourne, VIC 3004, Australiaen
dc.identifier.affiliationSurgery (University of Melbourne)en
dc.identifier.affiliationDepartment of Infectious Diseases, Melbourne Medical School, University of Melbourne, The Peter Doherty Institute for Infection and Immunity, Melbourne 3000, Australiaen
dc.identifier.affiliationVictorian Infectious Diseases Reference Laboratory, The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC 3000, Australiaen
dc.identifier.affiliationSchool of Pharmacy and Biomedical Sciences, Curtin University, Perth, Western Australia 6102, Australiaen
dc.identifier.affiliationSchool of Science, College of Science, Engineering and Health, RMIT University, Melbourne, VIC 3000, Australiaen
dc.identifier.doi10.1016/j.jcis.2021.02.067en
dc.type.contentTexten
dc.identifier.pubmedid33677197
local.name.researcherRamsland, Paul A
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairetypeJournal Article-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptSurgery (University of Melbourne)-
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