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Updated: Jul 29, 2025

Recapitulating Suckling-to-Weaning Transition In Vitro using Fetal Intestinal Organoids
Published on: November 15, 2019
Mechanism of iron on the intestinal epithelium development in suckling piglets
Lanmei Yin1,2,3, Yitong Zhang1, Jun Li1,4
1Hunan International Joint Laboratory of Animal Intestinal Ecology and Health, Laboratory of Animal Nutrition and Human Health, College of Life Sciences, Hunan Normal University, Changsha, 410081, China.
Insights
Lactation is crucial for piglet intestinal development, with iron metabolism changes impacting epithelial growth. Interleukin-22 (IL-22) may mediate iron
Area of Science:
- Gastroenterology
- Developmental Biology
- Nutritional Science
Background:
- Lactation significantly impacts intestinal epithelium development in suckling piglets.
- Iron metabolism undergoes dynamic changes during early postnatal development.
Purpose of the Study:
- To investigate the role of iron in piglet intestinal epithelium development.
- To elucidate the mechanisms by which iron influences intestinal maturation.
Main Methods:
- Comparative analysis of jejunal morphology, cell proliferation, and differentiation in piglets of different ages.
- In vitro studies using intestinal organoids treated with deferoxamine (iron chelator).
- Gene expression analysis of iron metabolism, epithelial maturation markers, and cytokine signaling pathways (IL-22).
Main Results:
- Piglet jejunum showed enhanced morphology, proliferation, and differentiation with age, correlating with altered iron metabolism genes.
- In vitro iron deficiency did not significantly impact epithelial maturation markers in early passages of organoids.
- Iron supplementation altered IL-22 receptor expression, while IL-22 treatment promoted adult epithelial marker expression in organoids.
Conclusions:
- Lactation is a critical period for intestinal development, intrinsically linked to iron metabolism.
- Iron deficiency may not directly impair intestinal epithelium development via intestinal stem cells.
- Interleukin-22 (IL-22) emerges as a key mediator in the interplay between iron and intestinal epithelium development.
Abstract:
This study aimed to investigate the mechanism of iron on intestinal epithelium development of suckling piglets. Compared with newborn piglets, 7-day-old and 21-day-old piglets showed changes in the morphology of the jejunum, increased proliferation, differentiated epithelial cells, and expanded enteroids. Intestinal epithelium maturation markers and iron metabolism genes were significantly changed. These results suggest that lactation is a critical stage in intestinal epithelial development, accompanied by changes in iron metabolism. In addition, deferoxamine (DFO) treatment inhibited the activity of intestinal organoids at passage 4 (P4) of 0-day-old piglets, but no significant difference was observed in epithelial maturation markers at passage 1 (P1) and P4, and only argininosuccinate synthetase 1 (Ass1) and β-galactosidase (Gleb) were up-regulated at passage 7 (P7). These results in vitro show that iron deficiency may not directly affect intestinal epithelium development through intestinal stem cells (ISCs). The iron supplementation significantly down-regulated the mRNA expression of interleukin-22 receptor subunit alpha-2 (IL-22RA2) in the jejunum of piglets. Furthermore, the mRNA expression of IL-22 in 7-day-old piglets was significantly higher than that in 0-day-old piglets. Adult epithelial markers were significantly up-regulated in organoids treated with recombinant murine cytokine IL-22. Thus, IL-22 may play a key role in iron-affecting intestinal epithelium development.
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