Literature DB >> 28754262

A comparison of three Peyer's patch "M-like" cell culture models: particle uptake, bacterial interaction, and epithelial histology.

Tauseef Ahmad1, Martina Gogarty1, Edwin G Walsh1, David J Brayden2.   

Abstract

Intestinal Peyer's patch (PP) microfold (M) cells transport microbes and particulates across the follicle-associated epithelium (FAE) as part of the mucosal immune surveillance system. In vitro human M-like cell co-culture models are used as screens to investigate uptake of antigens-in-nanoparticles, but the models are labour-intensive and there is inter-laboratory variability. We compared the three most established filter-grown Caco-2/Raji B cell co-culture systems. These were Model A (Kernéis et al., 1997), Model B (Gullberg et al., 2000), and Model C (Des Rieux et al. 2007). The criteria used were transepithelial resistance (TEER), the apparent permeability coefficient (Papp) of [14C]-mannitol, M cell-like histology, as well as latex particle and Salmonella typhimurium translocation. Each co-culture model displayed substantial increases in particle translocation. Truncated microvilli compared to mono-cultures was their most consistent feature. The inverted model developed by des Rieux et al. (2007) displayed reductions in TEER and an increased (Papp), accompanied by the largest increase in particle translocation compared to the other two models. The normally-oriented model developed by Gullberg et al. (2000) was the only one to consistently display an increased translocation of Salmonella typhimurium. By applying a double Matrigel™ coating on filters, altering the medium feeding regime for Raji B cells, and restricting the passage number of B cells, improvements to the Gullberg model B were achieved, as reflected by increased particle translocation and improved histology. In conclusion, this is the first time all three designs have been compared in one study and each displays phenotypic features of M-like cells. While Model C was the most robust co-culture, the Model B protocol could be improved by optimizing several variables and is less complicated to establish than the two inverted models.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Caco-2; Follicle-associated epithelium; M-like cells; Nanoparticle; Oral vaccine delivery; Peyer’s patch M cells

Mesh:

Substances:

Year:  2017        PMID: 28754262     DOI: 10.1016/j.ejpb.2017.07.013

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  4 in total

1.  Transcytosis of IgA Attenuates Salmonella Invasion in Human Enteroids and Intestinal Organoids.

Authors:  Cait M Costello; Graham G Willsey; Angelene F Richards; Jaeyoon Kim; Matteo S Pizzuto; Stefano Jaconi; Fabio Benigni; Davide Corti; Nicholas J Mantis; John C March
Journal:  Infect Immun       Date:  2022-05-17       Impact factor: 3.609

2.  Evaluating Shigella flexneri Pathogenesis in the Human Enteroid Model.

Authors:  Sridevi Ranganathan; Michele Doucet; Christen L Grassel; BreOnna Delaine-Elias; Nicholas C Zachos; Eileen M Barry
Journal:  Infect Immun       Date:  2019-03-25       Impact factor: 3.441

Review 3.  Research in a time of enteroids and organoids: how the human gut model has transformed the study of enteric bacterial pathogens.

Authors:  Sridevi Ranganathan; Emily M Smith; Jennifer D Foulke-Abel; Eileen M Barry
Journal:  Gut Microbes       Date:  2020-11-09

4.  A Versatile Human Intestinal Organoid-Derived Epithelial Monolayer Model for the Study of Enteric Pathogens.

Authors:  Stefania Senger; Christina S Faherty; Kourtney P Nickerson; Alejandro Llanos-Chea; Laura Ingano; Gloria Serena; Alba Miranda-Ribera; Meryl Perlman; Rosiane Lima; Marcelo B Sztein; Alessio Fasano
Journal:  Microbiol Spectr       Date:  2021-06-09
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.