Physiologically relevant coculture model for oral microbial-host interactions.
10.1038/s41368-025-00365-9
- Author:
Zeyang PANG
1
;
Nicole M CADY
2
;
Lujia CEN
3
;
Thomas M SCHMIDT
2
;
Xuesong HE
3
;
Jiahe LI
4
Author Information
1. Department of Biomedical Engineering, College of Engineering and School of Medicine, University of Michigan, Ann Arbor, MI, USA.
2. Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
3. Department of Microbiology, The ADA Forsyth Institute, Somerville, MA, USA.
4. Department of Biomedical Engineering, College of Engineering and School of Medicine, University of Michigan, Ann Arbor, MI, USA. jiaheli@umich.edu.
- Publication Type:Research Support, N.I.H., Extramural
- MeSH:
Coculture Techniques/methods*;
Humans;
Fusobacterium nucleatum/physiology*;
Gingiva/microbiology*;
Keratinocytes/microbiology*;
Host Microbial Interactions;
Mouth/microbiology*;
Host-Pathogen Interactions;
Epithelial Cells/microbiology*;
Cells, Cultured;
Porphyromonas gingivalis
- From:
International Journal of Oral Science
2025;17(1):42-42
- CountryChina
- Language:English
-
Abstract:
Understanding microbial-host interactions in the oral cavity is essential for elucidating oral disease pathogenesis and its systemic implications. In vitro bacteria-host cell coculture models have enabled fundamental studies to characterize bacterial infection and host responses in a reductionist yet reproducible manner. However, existing in vitro coculture models fail to establish conditions that are suitable for the growth of both mammalian cells and anaerobes, thereby hindering a comprehensive understanding of their interactions. Here, we present an asymmetric gas coculture system that simulates the oral microenvironment by maintaining distinct normoxic and anaerobic conditions for gingival epithelial cells and anaerobic bacteria, respectively. Using a key oral pathobiont, Fusobacterium nucleatum, as the primary test bed, we demonstrate that the system preserves bacterial viability and supports the integrity of telomerase-immortalized gingival keratinocytes. Compared to conventional models, this system enhanced bacterial invasion, elevated intracellular bacterial loads, and elicited more robust host pro-inflammatory responses, including increased secretion of CXCL10, IL-6, and IL-8. In addition, the model enabled precise evaluation of antibiotic efficacy against intracellular pathogens. Finally, we validate the ability of the asymmetric system to support the proliferation of a more oxygen-sensitive oral pathobiont, Porphyromonas gingivalis. These results underscore the utility of this coculture platform for studying oral microbial pathogenesis and screening therapeutics, offering a physiologically relevant approach to advance oral and systemic health research.
