Biomimetic Human Tissue Model for Long-Term Study of Infection
Overview
Authors
Affiliations
Gonorrhea is the second most common sexually transmitted infection in the world and is caused by Gram-negative diplococcus . Since is a human-specific pathogen, animal infection models are only of limited use. Therefore, a suitable cell culture model for studying the complete infection including adhesion, transmigration and transport to deeper tissue layers is required. In the present study, we generated three independent 3D tissue models based on porcine small intestinal submucosa (SIS) scaffold by co-culturing human dermal fibroblasts with human colorectal carcinoma, endometrial epithelial, and male uroepithelial cells. Functional analyses such as transepithelial electrical resistance (TEER) and FITC-dextran assay indicated the high barrier integrity of the created monolayer. The histological, immunohistochemical, and ultra-structural analyses showed that the 3D SIS scaffold-based models closely mimic the main characteristics of the site of gonococcal infection in human host including the epithelial monolayer, the underlying connective tissue, mucus production, tight junction, and microvilli formation. We infected the established 3D tissue models with different strains and derivatives presenting various phenotypes regarding adhesion and invasion. The results indicated that the disruption of tight junctions and increase in interleukin production in response to the infection is strain and cell type-dependent. In addition, the models supported bacterial survival and proved to be better suitable for studying infection over the course of several days in comparison to commonly used Transwell® models. This was primarily due to increased resilience of the SIS scaffold models to infection in terms of changes in permeability, cell destruction and bacterial transmigration. In summary, the SIS scaffold-based 3D tissue models of human mucosal tissues represent promising tools for investigating infections under close-to-natural conditions.
In vitro high-content tissue models to address precision medicine challenges.
Afewerki S, Stocco T, Rosa da Silva A, Aguiar Furtado A, Fernandes de Sousa G, Ruiz-Esparza G Mol Aspects Med. 2022; 91:101108.
PMID: 35987701 PMC: 9384546. DOI: 10.1016/j.mam.2022.101108.
Edwards V, McComb E, Gleghorn J, Forney L, Bavoil P, Ravel J Pathog Dis. 2022; 80(1).
PMID: 35927516 PMC: 9419571. DOI: 10.1093/femspd/ftac026.
Herbert S, Fick A, Heydarian M, Metzger M, Wockel A, Rudel T J Tissue Eng. 2022; 13:20417314221088514.
PMID: 35340423 PMC: 8949747. DOI: 10.1177/20417314221088514.
Tissue Models for Research-From 2D to 3D.
Heydarian M, Ruhl E, Rawal R, Kozjak-Pavlovic V Front Cell Infect Microbiol. 2022; 12:840122.
PMID: 35223556 PMC: 8873371. DOI: 10.3389/fcimb.2022.840122.
Heydarian M, Schweinlin M, Schwarz T, Rawal R, Walles H, Metzger M J Tissue Eng. 2021; 12:2041731420988802.
PMID: 33796248 PMC: 7970704. DOI: 10.1177/2041731420988802.