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Background <p>Intestinal epithelial cells are supported by dynamic cellular heterogeneity, which is critical for maintaining intestinal homeostasis. Recently, intestinal organoid models have gained attention as in vitro platforms because they can recapitulate the structural, functional, and cellular complexity of the small intestine. In this study, we developed porcine intestinal organoids and investigated time-dependent transcriptomic changes using single-cell RNA sequencing. Furthermore, to assess their applicability as an in vitro toxicity model, the organoids were exposed to the mycotoxins deoxynivalenol and zearalenone.</p> Results <p>The established organoids exhibited stable long-term culture up to passage 10 (32 d) and showed high genetic similarity to native small intestinal tissue across three regions: the duodenum, jejunum, and ileum. In various intestinal epithelial cell types, including transit-amplifying cells, enteroendocrine cells, goblet cells, Paneth cells,&#xa0;and other epithelial cell types, were identified in the organoids. Single-cell RNA sequencing classified the organoids into multiple distinct cell populations, including stem cells, transit-amplifying cells, secretory progenitors, enterocytes, enteroendocrine cells, goblet cells, and Paneth cells, demonstrating dynamic cellular heterogeneity. The organoids also recapitulated key intestinal functions, such as nutrient absorption and epithelial barrier formation, similar to those of the native small intestinal epithelium. Under these conditions, the cytotoxic effects of deoxynivalenol and zearalenone were evaluated. Treatment with these mycotoxins resulted in decreased cell viability, impaired intestinal barrier function, and altered rates of proliferation and differentiation, including those of enteroendocrine, goblet, and Paneth cell populations.</p> Conclusion <p>This study provides fundamental insights into the growth and differentiation of small intestinal epithelial cells by analyzing timeline-specific organoids using single-cell sequencing. Additionally, it evaluates the toxicity of mycotoxins under conditions that closely resemble those of the small intestine, providing more physiologically relevant data than existing in vitro models and serving as a reliable toxicity assessment model.</p>

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Dynamic cellular heterogeneity revealed through a time-resolved single-cell atlas: assessment of porcine intestinal organoids as an in vitro model for deoxynivalenol and zearalenone

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年6月3日

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  • Tae Hong Kang,
  • Jung Woong Yoon,
  • Seung Joon Lim,
  • Chae Hyun Lee,
  • Yo Han Lee,
  • Suhyeon Yun,
  • Heejun Jung,
  • Hyun Jun Jang,
  • Tae Hyun Kim,
  • Sang In Lee

摘要

Background

Intestinal epithelial cells are supported by dynamic cellular heterogeneity, which is critical for maintaining intestinal homeostasis. Recently, intestinal organoid models have gained attention as in vitro platforms because they can recapitulate the structural, functional, and cellular complexity of the small intestine. In this study, we developed porcine intestinal organoids and investigated time-dependent transcriptomic changes using single-cell RNA sequencing. Furthermore, to assess their applicability as an in vitro toxicity model, the organoids were exposed to the mycotoxins deoxynivalenol and zearalenone.

Results

The established organoids exhibited stable long-term culture up to passage 10 (32 d) and showed high genetic similarity to native small intestinal tissue across three regions: the duodenum, jejunum, and ileum. In various intestinal epithelial cell types, including transit-amplifying cells, enteroendocrine cells, goblet cells, Paneth cells, and other epithelial cell types, were identified in the organoids. Single-cell RNA sequencing classified the organoids into multiple distinct cell populations, including stem cells, transit-amplifying cells, secretory progenitors, enterocytes, enteroendocrine cells, goblet cells, and Paneth cells, demonstrating dynamic cellular heterogeneity. The organoids also recapitulated key intestinal functions, such as nutrient absorption and epithelial barrier formation, similar to those of the native small intestinal epithelium. Under these conditions, the cytotoxic effects of deoxynivalenol and zearalenone were evaluated. Treatment with these mycotoxins resulted in decreased cell viability, impaired intestinal barrier function, and altered rates of proliferation and differentiation, including those of enteroendocrine, goblet, and Paneth cell populations.

Conclusion

This study provides fundamental insights into the growth and differentiation of small intestinal epithelial cells by analyzing timeline-specific organoids using single-cell sequencing. Additionally, it evaluates the toxicity of mycotoxins under conditions that closely resemble those of the small intestine, providing more physiologically relevant data than existing in vitro models and serving as a reliable toxicity assessment model.