Abstract

Three-dimensional respiratory tissue models have been generated using, for example, human primary airway epithelial cells (hAEC) or respective cell lines. To investigate ciliopathies, such as primary ciliary dyskinesia, the presence of functional kinocilia in vitro is an essential prerequisite. Since access to hAEC of healthy donors is limited, we aimed to identify a respiratory epithelial cell line that is capable to display functional kinocilia on at least 60% of the apical surface. Thus, we cultured four different human respiratory cell lines with human primary airway fibroblasts under airlift conditions, characterized the morphology, and analyzed ciliary function. Only one of the tested cell lines showed beating kinocilia; however, <10% of the whole surface was covered and ciliary beating was undirected. Positive control tissue models using hAEC and fibroblasts displayed expected directed ciliary beating pattern around 11 Hz. Our data show that the available cell lines are not suitable for basic and applied research questions whenever functional kinocilia are required and that, rather, hAEC- or human induced pluripotent stem cell-derived tissue models need to be generated.Impact StatementTo study ciliopathies or Bordetella pertussis infection in vitro, three-dimensional respiratory tissue models with functional kinocilia covering at least 60% of the model's surface are mandatory. We cultured four respiratory cell lines on a fibroblast-loaded biological scaffold and showed that none of them met this requirement. In contrast, primary airway cell-derived models sufficiently reflected the mucociliary phenotype. To further search for an alternative to primary respiratory cells, investigations on other cell lines should be conducted or even new cell lines have to be generated.

Highlights

  • Three-dimensional (3D) cell cultures of the respiratory epithelium/mucosa afford research on—for example— the impact of airborne pollutants, host-pathogen interactions, and drug permeation.[1,2,3,4,5] As source for respiratory epithelial cells, primary cells, induced pluripotent stem cells, or cell lines can be used

  • In 3D tissue models based on HBEC3-KT, VA10, and Cl-huAEC, both CK5- and CK18-specific signals were found in the epithelial compartment (Fig. 2B, F, N)

  • We aimed to identify an airway epithelial cell line that was capable to differentiate to the mucociliary phenotype

Read more

Summary

Introduction

Three-dimensional (3D) cell cultures of the respiratory epithelium/mucosa afford research on—for example— the impact of airborne pollutants, host-pathogen interactions, and drug permeation.[1,2,3,4,5] As source for respiratory epithelial cells, primary cells, induced pluripotent stem cells (iPSC), or cell lines can be used Both primary cells and iPSC provide the opportunity to generate personalized tissue models, for example, to study individual drug responses or drug efficacy. They show a high in vitro-in vivo correlation These models feature a pseudostratified epithelial morphology, barrier properties, basal cells, mucus-producing goblet cells, and ciliated cells facilitating mucociliary clearance.[6,7,8,9]

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.