3‑D Intestinal Scaffolds for Evaluating the Therapeutic Potential of Probiotics

• Published in: Molecular pharmaceutics 2014-07, Vol.11 (7), p.2030-2039
• Main Authors: Costello, Cait M, Sorna, Rachel M, Goh, Yih-Lin, Cengic, Ivana, Jain, Nina K, March, John C
• Format: Article
• Language: English
• Subjects: Bacteria - drug effects; Bacterial Adhesion - drug effects; Biomimetics - methods; Caco-2 Cells; Cell Differentiation - drug effects; Drug Evaluation - methods; Epithelial Cells - drug effects; Epithelial Cells - microbiology; Escherichia coli; Humans; Intestine, Small - drug effects; Intestine, Small - microbiology; Lactobacillus; Probiotics - pharmacology; Pseudomonas; Salmonella; Tissue Scaffolds - microbiology
• ISSN: 1543-8384; 1543-8392
• DOI: 10.1021/mp5001422

Biomimetic in vitro intestinal models are becoming useful tools for studying host–microbial interactions. In the past, these models have typically been limited to simple cultures on 2-D scaffolds or Transwell inserts, but it is widely understood that epithelial cells cultured in 3-D environments exhibit different phenotypes that are more reflective of native tissue, and that different microbial species will preferentially adhere to select locations along the intestinal villi. We used a synthetic 3-D tissue scaffold with villous features that could support the coculture of epithelial cell types with select bacterial populations. Our end goal was to establish microbial niches along the crypt–villus axis in order to mimic the natural microenvironment of the small intestine, which could potentially provide new insights into microbe-induced intestinal disorders, as well as enabling targeted probiotic therapies. We recreated the surface topography of the small intestine by fabricating a biodegradable and biocompatible villous scaffold using poly lactic-glycolic acid to enable the culture of Caco-2 with differentiation along the crypt–villus axis in a similar manner to native intestines. This was then used as a platform to mimic the adhesion and invasion profiles of both Salmonella and Pseudomonas, and assess the therapeutic potential of Lactobacillus and commensal Escherichia coli in a 3-D setting. We found that, in a 3-D environment, Lactobacillus is more successful at displacing pathogens, whereas Nissle is more effective at inhibiting pathogen adhesion.