Cellular heterogeneity in the 16HBE14o - airway epithelial line impacts biological readouts.
Jenny L KerschnerAlekh ParanjapyeAnn HarrisPublished in: Physiological reports (2023)
The airway epithelial cell line, 16HBE14o - , is an important cell model for studying airway disease. 16HBE14o - cells were originally generated from primary human bronchial epithelial cells by SV40-mediated immortalization, a process that is associated with genomic instability through long-term culture. Here, we explore the heterogeneity of these cells, with respect to expression of the cystic fibrosis transmembrane conductance regulator (CFTR) transcript and protein. We isolate clones of 16HBE14o - with stably higher and lower levels of CFTR in comparison to bulk 16HBE14o - , designated CFTR high and CFTR low . Detailed characterization of the CFTR locus in these clones by ATAC-seq and 4C-seq showed open chromatin profiles and higher order chromatin structure that correlate with CFTR expression levels. Transcriptomic profiling of CFTR high and CFTR low cells showed that the CFTR high cells had an elevated inflammatory/innate immune response phenotype. These results encourage caution in interpreting functional data from clonal lines of 16HBE14o - cells, generated after genomic or other manipulations.
Keyphrases
- cystic fibrosis
- induced apoptosis
- pseudomonas aeruginosa
- immune response
- cell cycle arrest
- single cell
- lung function
- poor prognosis
- endoplasmic reticulum stress
- gene expression
- genome wide
- rna seq
- dna damage
- transcription factor
- stem cells
- cell death
- chronic obstructive pulmonary disease
- binding protein
- mesenchymal stem cells
- pi k akt
- cell proliferation
- endothelial cells
- artificial intelligence
- amino acid