4.7 Article

Investigating virus-host cell interactions: Comparative binding forces between hepatitis C virus-like particles and host cell receptors in 2D and 3D cell culture models

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 592, 期 -, 页码 371-384

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.02.067

关键词

Atomic force microscopy; Bio-interface; Enveloped virus-like particles; Nanostructure; Vaccine development

资金

  1. Australian Government, Department of Education and Training
  2. Jack Brockhoff Foundation (JBF) [4655-2019]
  3. National Health and Medical Research Council of Australia [APP1181580]

向作者/读者索取更多资源

Cell cultures have been successfully used to study hepatitis C virus (HCV) for many years, with recent research suggesting that polarized cell systems are more suitable for studying HCV infection and dynamics.
Cell 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 extracellular-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 viruslike 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 nonpolarized systems. (C) 2021 Elsevier Inc. All rights reserved.

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