Mimicking in vivo-like physiological properties of the human bronchial epithelium in in vitro 3-D cell cultures

Wlodarczyk, Anna Julia, Prytherch, Zoe Cariad ORCID: https://orcid.org/0000-0003-0690-0184, Huttunen, Kati and Berube, Kelly Ann ORCID: https://orcid.org/0000-0002-7471-7229 2015. Mimicking in vivo-like physiological properties of the human bronchial epithelium in in vitro 3-D cell cultures. Presented at: Early Career Physiologists' Symposium (ECPS) 2015: Cell Signalling in Health and Disease, Cardiff, UK, 5 July 2015. -1.

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Abstract

The human respiratory muco-ciliary epithelium consists of different cell types, connected by tight junctions; forming a protective barrier against the external environment. The epithelium is attached to a basement membrane through which necessary nutrients are delivered. Apart from a thin layer of mucus, the apical part of the bronchial epithelium is exposed to the ambient air. Mimicking these conditions through the use of 3-dimensional (3-D) filter-well membrane technology, a functional and fully-differentiated muco-ciliary phenotype in vitro cell culture model can be obtained. By providing the in vivo-like pulmonary microenvironment primary bronchial cells are stimulated to differentiate into a pseudo-stratified epithelium containing, basal, ciliated, Clara, goblet, intermediate and serous cells. In addition to this in vivo-like morphology, the cultures attain physiological properties akin to the human bronchial epithelium. Cells form tight junctions, enabling the whole culture to function as a barrier, providing trans-epithelial electrical resistance (TEER). Day 15 of ALI culture conditions results in beating cilia that are fully-grown and spread the mucus produced by the goblet cells. Unlike ‘conventional’ cell cultures, where tested substances need to be suspended in submerged culture media, our 3-D model of the human bronchial epithelium enables in vitro toxicology testing of apically deposited aerosols and/or solubilised substances onto mucus protected cell surfaces. This mimics in vivo deposition through inhalation. Moreover, we observe the tissue (i.e. multi-cellular) response, rather than the effect of submerged cell monolayers (i.e. single cell type). The additional protective mechanisms, such as apical mucus, traps inhaled substances and the tight junctions (i.e. barrier function) provide a more in vivo-like response when compared to submerged monolayer cultures. Our 3-D model of the human bronchial epithelium maintains the in vivo complexity observed in the in-situ human lung and is a reliable in vitro tool that can be employed to obtain robust predictive in vivo responses for human endpoint data.

Item Type:	Conference or Workshop Item (Lecture)
Date Type:	Completion
Status:	Unpublished
Schools:	Biosciences
Subjects:	Q Science > Q Science (General)
Related URLs:	http://www.physiology2015.org/early-care...
Last Modified:	17 Nov 2022 05:11
URI:	https://orca.cardiff.ac.uk/id/eprint/79030

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