» Articles » PMID: 35927516

Three-dimensional Models of the Cervicovaginal Epithelia to Study Host-microbiome Interactions and Sexually Transmitted Infections

Overview
Journal Pathog Dis
Date 2022 Aug 4
PMID 35927516
Authors
Affiliations
Soon will be listed here.
Abstract

2D cell culture systems have historically provided controlled, reproducible means to analyze host-pathogen interactions observed in the human reproductive tract. Although inexpensive, straightforward, and requiring a very short time commitment, these models recapitulate neither the functionality of multilayered cell types nor the associated microbiome that occurs in a human. Animal models have commonly been used to recreate the complexity of human infections. However, extensive modifications of animal models are required to recreate interactions that resemble those in the human reproductive tract. 3D cell culture models have emerged as alternative means of reproducing vital elements of human infections at a fraction of the cost of animal models and on a scale that allows for replicative experiments. Here, we describe a new 3D model that utilizes transwells with epithelial cells seeded apically and a basolateral extracellular matrix (ECM)-like layer. The model produced tissues with morphologic and physiological resemblance to human cervical and vaginal epithelia, including mucus levels produced by cervical cells. Infection by Chlamydia trachomatis and Neisseria gonorrhoeae was demonstrated, as well as the growth of bacterial species observed in the human vaginal microbiota. This enabled controlled mechanistic analyses of the interactions between host cells, the vaginal microbiota, and STI pathogens. Affordable and semi high-throughput 3D models of the cervicovaginal epithelia that are physiologically relevant by sustaining vaginal bacterial colonization, and facilitate studies of chlamydial and gonococcal infections.

Citing Articles

A straightforward cell culture insert model to incorporate biochemical and biophysical stromal properties into transplacental transport studies.

Nelson K, Ferrick B, Karimi H, Hatem C, Gleghorn J Placenta. 2024; .

PMID: 39266436 PMC: 11880344. DOI: 10.1016/j.placenta.2024.09.001.


A straightforward cell culture insert model to incorporate biochemical and biophysical stromal properties into transplacental transport studies.

Nelson K, Ferrick B, Karimi H, Hatem C, Gleghorn J bioRxiv. 2024; .

PMID: 38712271 PMC: 11071360. DOI: 10.1101/2024.04.19.590317.


The human vaginal microbiota: from clinical medicine to models to mechanisms.

Ottinger S, Robertson C, Branthoover H, Patras K Curr Opin Microbiol. 2024; 77:102422.

PMID: 38215548 PMC: 11160953. DOI: 10.1016/j.mib.2023.102422.


Contributions of diverse models of the female reproductive tract to the study of Chlamydia trachomatis-host interactions.

Walker F, Derre I Curr Opin Microbiol. 2023; 77:102416.

PMID: 38103413 PMC: 10922760. DOI: 10.1016/j.mib.2023.102416.


Delivery and short-term maternal and fetal safety of vaginally administered PEG-PLGA nanoparticles.

Irvin-Choy N, Nelson K, Gleghorn J, Day E Drug Deliv Transl Res. 2023; 13(12):3003-3013.

PMID: 37365402 PMC: 10913101. DOI: 10.1007/s13346-023-01369-w.


References
1.
Unemo M, Seifert H, Hook 3rd E, Hawkes S, Ndowa F, Dillon J . Gonorrhoea. Nat Rev Dis Primers. 2019; 5(1):79. DOI: 10.1038/s41572-019-0128-6. View

2.
Macdonald E, Savoy A, Gillgrass A, Fernandez S, Smieja M, Rosenthal K . Susceptibility of human female primary genital epithelial cells to herpes simplex virus, type-2 and the effect of TLR3 ligand and sex hormones on infection. Biol Reprod. 2007; 77(6):1049-59. DOI: 10.1095/biolreprod.107.063933. View

3.
Gargus E, Rogers H, McKinnon K, Edmonds M, Woodruff T . Engineered reproductive tissues. Nat Biomed Eng. 2020; 4(4):381-393. PMC: 7416444. DOI: 10.1038/s41551-020-0525-x. View

4.
Choi N, Cabodi M, Held B, Gleghorn J, Bonassar L, Stroock A . Microfluidic scaffolds for tissue engineering. Nat Mater. 2007; 6(11):908-15. DOI: 10.1038/nmat2022. View

5.
Meaburn K . Fluorescence in situ hybridization on 3D cultures of tumor cells. Methods Mol Biol. 2010; 659:323-36. DOI: 10.1007/978-1-60761-789-1_25. View