| Literature DB >> 27464691 |
Lindsay Broadbent1, Remi Villenave1, Hong Guo-Parke1, Isobel Douglas2, Michael D Shields1,2, Ultan F Power3.
Abstract
The choice of model used to study human respiratory syncytial virus (RSV) infection is extremely important. RSV is a human pathogen that is exquisitely adapted to infection of human hosts. Rodent models, such as mice and cotton rats, are semi-permissive to RSV infection and do not faithfully reproduce hallmarks of RSV disease in humans. Furthermore, immortalized airway-derived cell lines, such as HEp-2, BEAS-2B, and A549 cells, are poorly representative of the complexity of the respiratory epithelium. The development of a well-differentiated primary pediatric airway epithelial cell models (WD-PAECs) allows us to simulate several hallmarks of RSV infection of infant airways. They therefore represent important additions to RSV pathogenesis modeling in human-relevant tissues. The following protocols describe how to culture and differentiate both bronchial and nasal primary pediatric airway epithelial cells and how to use these cultures to study RSV cytopathogenesis.Entities:
Keywords: Cytopathogenesis; Primary human airway epithelial cells; Respiratory syncytial virus; Well-differentiated human airway epithelial cell culture (WD-PAECs)
Mesh:
Year: 2016 PMID: 27464691 DOI: 10.1007/978-1-4939-3687-8_9
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745