Skip to main content
Log in

Permeability Properties of an In Vitro Model of the Alveolar Epithelium

  • Original Article
  • Published:
Cellular and Molecular Bioengineering Aims and scope Submit manuscript

Abstract

Cell culture models of epithelial barriers in the body are widely used to study the permeation of nutrients, drugs, infectious agents and pollutants into the body tissues and circulation. The NCI-H441 cell line cultured at the air-liquid interface mimics certain phenotypic and functional characteristics of the human alveolar epithelium. Here the permeability properties of the NCI-H441 model were characterised and compared against published data using experimental measurements and mathematical modelling. Cells were cultured under air-liquid interface conditions and trans-epithelial electrical resistance (TEER) and apparent permeability (Papp) to sodium fluorescein (MW 383 Da) and fluorescently labelled dextrans (MW 4000–150,000 Da) was measured. It was found that TEER was independent of cell seeding density while Papp decreased with higher seeding density and plateaued beyond a density of 500,000 cells/cm2. Using the framework of functional pore analysis, a mathematical model was fitted to Papp values measured in this work as well as previously published datasets from human cell lines and primary human and rat cells. It was found that the air-liquid interface NCI-H441 model most closely matched the primary cell line results in contrast to published data using A549 and liquid-interface NCI-H441 cell cultures, supporting the use of this model to study the permeability of the alveolar epithelium to large molecules.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1
Figure 2
Figure 3

Similar content being viewed by others

References

  1. Beck, R. E., and J. S. Schultz. Hindrance of solute diffusion within membranes as measured with microporous membranes of known pore geometry. Biochim. Biophys. Acta. 255:273–280, 1972.

    Article  Google Scholar 

  2. Cipolla, D. Will pulmonary drug delivery for systemic application ever fulfill its rich promise. Expert Opin. Drug Deliv. 13(10):1337–1340, 2016.

    Article  Google Scholar 

  3. Cryan, S. A., N. Sivadas, and L. Garcia-Contreras. In vivo animal models for drug delivery across the lung mucosal barrier. Adv. Drug. Deliv. Rev. 59:1133–1151, 2007.

    Article  Google Scholar 

  4. Ehrhardt, C., J. Fiegel, S. Fuchs, R. Abu-Dahab, U. F. Schaefer, J. Hanes, and C. M. Lehr. Drug absorption by the respiratory mucosa: cell culture models and particulate drug carriers. J. Aerosol. Med. 15:131–139, 2002.

    Article  Google Scholar 

  5. Ehrhardt, C., K.-J. Kim, and M. Laue. In Vitro Models of the Alveolar Epithelial Barrier Drug Absorption Studies. New York: Springer, pp. 258–282, 2008.

    Google Scholar 

  6. Elbert, K. J., U. F. Schafer, H. J. Schafers, K. J. Kim, V. H. L. Lee, and C. M. Lehr. Monolayers of human alveolar epithelial cells in primary culture for pulmonary absorption and transport studies. Pharm. Res. 16:601–608, 1999.

    Article  Google Scholar 

  7. Frank, J. A. Claudins and alveolar epithelial barrier function in the lung. Ann. N. Y. Acad. Sci. 1257:175–183, 2012.

    Article  Google Scholar 

  8. Frost, T. S., L. Jiang, R. M. Lynch, and Y. Zohar. Permeability of epithelial/endothelial barriers in transwells and microfluidic bilayer devices. Micromachines. 10:533, 2019.

    Article  Google Scholar 

  9. Ghadiri, M., P. M. Young, and D. Traini. Strategies to enhance drug absorption via nasal and pulmonary routes. Pharmaceutics. 11(13):113, 2019.

    Article  Google Scholar 

  10. Günzel, D., and A. D. Yu. Claudins and the modulation of tight junction permeability. Physiol. Rev. 93(2):525–569, 2013.

    Article  Google Scholar 

  11. Huh, D., B. D. Matthews, A. Mammoto, M. Montoya-Zavala, H. Y. Hsin, and D. E. Ingber. Reconstituting organ-level lung functions on a chip. Science. 328:1662–1668, 2010.

    Article  Google Scholar 

  12. Kim, K. J., Z. Borok, and E. D. Crandall. A useful in vitro model for transport studies of alveolar epithelial barrier. Pharm. Res. 18:253–255, 2001.

    Article  Google Scholar 

  13. Kobayashi, S., S. Kondo, and K. Juni. Permeability of peptides and proteins in human cultured alveolar A549 cell monolayer. Pharm. Res. 12:1115–1119, 1995.

    Article  Google Scholar 

  14. Matsukawa, Y., V. H. L. Lee, E. D. Crandall, and K. J. Kim. Size dependent dextran transport across rat alveolar epithelial cell monolayers. J. Pharm. Sci. 86:305–309, 1997.

    Article  Google Scholar 

  15. Nalayanda, D. D., C. Puleo, W. B. Fulton, L. M. Sharp, T.-H. Wang, and F. Abdullah. An open-access microfluidic model for lung-specific functional studies at an air-liquid interface. Biomed. Microdevices. 11:1081, 2009.

    Article  Google Scholar 

  16. Overgaard, C. E., L. A. Mitchell, and M. Koval. Roles for claudins in alveolar epithelial barrier function. Ann. N. Y. Acad. Sci. 1257(1):167–174, 2012.

    Article  Google Scholar 

  17. Patton, J. S., C. S. Fishburn, and J. G. Weers. The lungs as a portal of entry for systemic drug delivery. Proc. Am. Thorac. Soc. 1(4):338–344, 2004.

    Article  Google Scholar 

  18. Ren, H., N. P. Birch, and V. Suresh. An optimised human cell culture model for alveolar epithelial transport. PLoS ONE. 11:e0165225, 2016.

    Article  Google Scholar 

  19. Sakagami, M. In vivo, in vitro and ex vivo models to assess pulmonary absorption and disposition of inhaled therapeutics for systemic delivery. Adv. Drug Deliv. Rev. 58:1030–1060, 2006.

    Article  Google Scholar 

  20. Salomon, J. J., V. E. Muchitsch, J. C. Gausterer, E. Schwagerus, H. Huwer, N. Daum, C. M. Lehr, and C. Ehrhardt. The cell line NCl-H441 is a useful in vitro model for transport studies of human distal lung epithelial barrier. Mol. Pharm. 11(3):995–1006, 2014.

    Article  Google Scholar 

  21. Stucki, J. D., N. Hobi, A. Galimov, et al. Medium throughput breathing human primary cell alveolus-on-chip model. Sci. Rep. 8:14359, 2018.

    Article  Google Scholar 

  22. Watson, C. J., M. Rowland, and G. Warhurst. Functional modeling of tight junctions in intestinal cell monolayers using polyethylene glycol oligomers. Am. J. Physiol. Cell Physiol. 281:C388-397, 2001.

    Article  Google Scholar 

  23. Zamprogno, P., S. Wüthrich, S. Achenbach, et al. Second-generation lung-on-a-chip with an array of stretchable alveoli made with a biological membrane. Commun. Biol. 4:168, 2021.

    Article  Google Scholar 

  24. Zihni, C., C. Mills, K. Matter, et al. Tight junctions: from simple barriers to multifunctional molecular gates. Nat. Rev. Mol. Cell Biol. 17:564–580, 2016.

    Article  Google Scholar 

Download references

Acknowledgments

Author VS declares that he has no conflict of interest. This work was supported by the RSNZ Marsden Fund (Grant No. UOA-1411).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Vinod Suresh.

Additional information

Associate Editor Michael R. King oversaw the review of this article.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Suresh, V. Permeability Properties of an In Vitro Model of the Alveolar Epithelium. Cel. Mol. Bioeng. 14, 653–659 (2021). https://doi.org/10.1007/s12195-021-00690-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12195-021-00690-z

Keywords

Navigation