Primary epithelial cell models for cystic fibrosis research.

Scott H Randell, M Leslie Fulcher, Wanda O'Neal, John C Olsen
Author Information
  1. Scott H Randell: Cystic Fibrosis/Pulmonary Research and Treatment Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. randell@med.unc.edu

Abstract

When primary human airway epithelial (hAE) cells are grown in vitro on porous supports at an air-liquid interface (ALI), they recapitulate in vivo morphology and key physiologic processes. These cultures are useful for studying respiratory tract biology and diseases and for testing new cystic fibrosis (CF) therapies. This chapter gives protocols enabling creation of well-differentiated primary CF and non-CF airway epithelial cell cultures with non-proprietary reagents. We also discuss the production of retroviral and lentiviral vectors, the derivation of hAE cell lines, reporter gene assays, and the evolving science of gene overexpression and knockdown in ALI hAE cultures.

MeSH Term

Adenoviridae
Cell Culture Techniques
Cell Differentiation
Cell Line
Cryopreservation
Culture Media
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Epithelial Cells
Gene Expression
Gene Silencing
Genes, Reporter
Genetic Vectors
Humans
Indicators and Reagents
RNA, Small Interfering
Respiratory Mucosa
Retroviridae
Tissue Engineering
Transfection

Chemicals

Culture Media
Indicators and Reagents
RNA, Small Interfering
Cystic Fibrosis Transmembrane Conductance Regulator

Word Cloud

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