# An artificial mucus-integrated in vitro model enables stable live probiotic–host co-culture and recapitulates dynamic hBD-2-mediated antimicrobial feedback

**Authors:** Wenxin Cao, Yumiko Watanabe-Yasuoka, Toshihiro Sashihara, Masaki Nishikawa, Yasuyuki Sakai

PMC · DOI: 10.1080/29933935.2026.2622881 · Gut Microbes Reports · 2026-01-31

## TL;DR

A new in vitro model with artificial mucus allows stable co-culture of live probiotics and intestinal cells, showing how mucus helps regulate host-microbe interactions.

## Contribution

The first scalable in vitro model integrating artificial mucus for stable live probiotic-host co-culture and dynamic hBD-2 feedback.

## Key findings

- The model supports 48-hour co-culture of live Lactiplantibacillus plantarum OLL2712 with Caco-2 cells at high exposure ratios.
- hBD-2 protein secretion was 100-fold higher in the presence of mucus compared to previous reports.
- The model demonstrates a complete feedback loop involving microbial stimulation, hBD-2 secretion, and bacterial suppression.

## Abstract

In vitro models for host–microbe interaction often have limited physiological relevance due to the absence of a protective mucus layer, reliance on non-viable bacteria, and short co-culture durations. Here, we present the first scalable and biocompatible in vitro model integrating an artificial mucus barrier that enables stable 48-hour co-culture of live Lactiplantibacillus plantarum OLL2712 with Caco-2 cells at exposure ratios up to 1,000. This model maintained epithelial viability, supported bacterial proliferation, and enabled dynamic host responses. Notably, during co-culture, while hBD-2 gene expression was observed under both with-mucus and without-mucus conditions, protein secretion occurred only in the presence of mucus, reaching approximately a 100-fold higher level than previously reported. This finding underscores the essential role of the mucus barrier in preserving epithelial function and maintaining the downstream host response. The model recapitulates a complete host-microbe feedback loop involving microbial stimulation, antimicrobial peptide (hBD-2) secretion, and subsequent bacterial suppression, thereby linking epithelial defense activation to microbial regulation. It provides a reproducible, physiologically relevant, and animal-free platform for probiotic screening and mechanistic studies of mucus-associated intestinal disorders such as inflammatory bowel disease.

## Linked entities

- **Genes:** DEFB4A (defensin beta 4A) [NCBI Gene 1673]
- **Proteins:** DEFB4A (defensin beta 4A)
- **Diseases:** inflammatory bowel disease (MONDO:0005265)

## Full-text entities

- **Genes:** DEFB4A (defensin beta 4A) [NCBI Gene 1673] {aka BD-2, DEFB-2, DEFB102, DEFB2, DEFB4, HBD-2}
- **Diseases:** inflammatory bowel disease (MESH:D015212)
- **Chemicals:** OLL2712 (-)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938872/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938872/full.md

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Source: https://tomesphere.com/paper/PMC12938872