Polarization in Cell

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cellular Biophysics".

Deadline for manuscript submissions: closed (30 April 2024) | Viewed by 1554

Special Issue Editor


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Guest Editor
School of Medicine, University of California, San Francisco, CA, USA
Interests: epithelia polarity; epithelial morphogenesis and tube formation

Special Issue Information

Dear Colleagues,

Almost all cells are spatially asymmetric, i.e., they are polarized. The focus of this Special Issue is on eukaryotes, even though most prokaryote and archaea cells also have polarity. We have learned a great deal about cell polarity from studying single cell eukaryotes, especially the yeast S. cerevisiae, which has been a major model system for most aspects of cell biology. Many of the molecular mechanisms of polarity that are reviewed in this Special Issue, such as the exocyst, were first discovered in S. cerevisiae.

Cell polarity plays an especially important role in metazoa, i.e., multicellular animals. Cells in metazoa are organized into tissues. The most basic type of tissue in animals is epithelial tissue, in which epithelial cells are arranged in a monolayer of cells that forms a barrier separating two compartments. An outer layer of epithelium covers the outside of the organism, such as the epidermis in mammals. In the simplest animals, such as hydras, there is a single internal cavity or tube, lined by a layer of epithelial cells. In more complex metazoans, such as mammals, there are many interior organ systems, such as the gastrointestinal, respiratory, urinary and vascular systems, each lined by a single layer of specialized epithelial cells. In almost all cases, these epithelial cells are highly polarized, and much of this volume is focused on epithelial cells, both because their polarity has been very well examined and because of their relevance to human medicine.

Prof. Dr. Keith E. Mostov
Guest Editor

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Keywords

  • cell polarity
  • epithelial polarity
  • neuronal polarity
  • membrane traffic
  • apical surface
  • basolateral surface

Published Papers (1 paper)

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Research

18 pages, 6987 KiB  
Article
Coronavirus M Protein Trafficking in Epithelial Cells Utilizes a Myosin Vb Splice Variant and Rab10
by Lynne A. Lapierre, Joseph T. Roland, Elizabeth H. Manning, Catherine Caldwell, Honor L. Glenn, Pierre-Olivier Vidalain, Frederic Tangy, Brenda G. Hogue, C. A. M. de Haan and James R. Goldenring
Cells 2024, 13(2), 126; https://doi.org/10.3390/cells13020126 - 10 Jan 2024
Viewed by 1048
Abstract
The membrane (M) glycoprotein of coronaviruses (CoVs) serves as the nidus for virion assembly. Using a yeast two-hybrid screen, we identified the interaction of the cytosolic tail of Murine Hepatitis Virus (MHV-CoV) M protein with Myosin Vb (MYO5B), specifically with the alternative splice [...] Read more.
The membrane (M) glycoprotein of coronaviruses (CoVs) serves as the nidus for virion assembly. Using a yeast two-hybrid screen, we identified the interaction of the cytosolic tail of Murine Hepatitis Virus (MHV-CoV) M protein with Myosin Vb (MYO5B), specifically with the alternative splice variant of cellular MYO5B including exon D (MYO5B+D), which mediates interaction with Rab10. When co-expressed in human lung epithelial A549 and canine kidney epithelial MDCK cells, MYO5B+D co-localized with the MHV-CoV M protein, as well as with the M proteins from Porcine Epidemic Diarrhea Virus (PEDV-CoV), Middle East Respiratory Syndrome (MERS-CoV) and Severe Acute Respiratory Syndrome 2 (SARS-CoV-2). Co-expressed M proteins and MYO5B+D co-localized with endogenous Rab10 and Rab11a. We identified point mutations in MHV-CoV M that blocked the interaction with MYO5B+D in yeast 2-hybrid assays. One of these point mutations (E121K) was previously shown to block MHV-CoV virion assembly and its interaction with MYO5B+D. The E to K mutation at homologous positions in PEDV-CoV, MERS-CoV and SARS-CoV-2 M proteins also blocked colocalization with MYO5B+D. The knockdown of Rab10 blocked the co-localization of M proteins with MYO5B+D and was rescued by re-expression of CFP-Rab10. Our results suggest that CoV M proteins traffic through Rab10-containing systems, in association with MYO5B+D. Full article
(This article belongs to the Special Issue Polarization in Cell)
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