Influenza Virus Infections in Polarized Cells.
N-glycan
O-glycan
influenza A virus
polarized cell
sialic acid
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
15 06 2022
15 06 2022
Historique:
received:
18
02
2022
revised:
09
06
2022
accepted:
11
06
2022
entrez:
24
6
2022
pubmed:
25
6
2022
medline:
28
6
2022
Statut:
epublish
Résumé
In humans and other mammals, the respiratory tract is represented by a complex network of polarized epithelial cells, forming an apical surface facing the external environment and a basal surface attached to the basement layer. These cells are characterized by differential expression of proteins and glycans, which serve as receptors during influenza virus infection. Attachment between these host receptors and the viral surface glycoprotein hemagglutinin (HA) initiates the influenza virus life cycle. However, the virus receptor binding specificities may not be static. Sialylated N-glycans are the most well-characterized receptors but are not essential for the entry of influenza viruses, and other molecules, such as O-glycans and non-sialylated glycans, may be involved in virus-cell attachment. Furthermore, correct cell polarity and directional trafficking of molecules are essential for the orderly development of the system and affect successful influenza infection; on the other hand, influenza infection can also change cell polarity. Here we review recent advances in our understanding of influenza virus infection in the respiratory tract of humans and other mammals, particularly the attachment between the virus and the surface of the polar cells and the polarity variation of these cells due to virus infection.
Identifiants
pubmed: 35746778
pii: v14061307
doi: 10.3390/v14061307
pmc: PMC9231244
pii:
doi:
Substances chimiques
Hemagglutinin Glycoproteins, Influenza Virus
0
Polysaccharides
0
Receptors, Virus
0
Types de publication
Journal Article
Review
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIAID NIH HHS
ID : R01 AI147640
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI144433
Pays : United States
Organisme : NIH HHS
ID : R21AI144433
Pays : United States
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