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Updated: Jul 4, 2026

Testing Epithelial Permeability in Fetal Tissue-Derived Enteroids
Published on: June 16, 2022
Developmental maturation of intestinal junctional complexes in preterm infants
Catherine Kollmann1, Carolin Niklas1, Karen Ernestus2
1Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, Würzburg, Germany.
Insights
The intestinal epithelial barrier (IEB) in preterm infants shows early maturation of key junctional proteins. Further development occurs between 26-27 weeks gestation, aiding understanding of infant gastrointestinal health.
Area of Science:
- Gastroenterology
- Neonatal Research
- Cell Biology
Background:
- Preterm infants face high risks of gastrointestinal issues like necrotizing enterocolitis due to immature intestinal epithelial barriers (IEB).
- Limited understanding exists regarding the development of IEB and its junctional complexes in early life.
Purpose of the Study:
- To sequentially characterize the maturation of tight junctions, adherens junctions, and desmosomes in the human intestine of very preterm infants.
- To compare junctional complex composition in preterm infants with adult expression patterns.
Main Methods:
- Analysis of intestinal tissue from healthy resection margins of six preterm infants (25-28 weeks gestation).
- Immunostaining techniques were used to assess the expression and localization of key junctional proteins.
- Comparison of protein composition with adult intestinal tissue.
Main Results:
- Proteins like Claudin-2, Claudin-3, Occludin, E-cadherin, β-Catenin, Plakoglobin, and Plakophilin-2 showed adult-like maturity by 25 weeks gestation.
- Claudin-1, -4, -5, and ZO-1 showed increased and more defined staining patterns with advancing gestational age (26-27 weeks).
- Desmocollin-2 increased until 26 weeks, while Desmoglein-2 and Desmoplakin expression remained immature at 28 weeks compared to adults.
Conclusions:
- This study offers the first sequential characterization of major IEB component maturation in human preterm infants.
- Findings highlight specific gestational windows for junctional complex development.
- Understanding these maturation processes may reveal mechanisms behind intestinal pathologies in preterm infants.
Abstract:
Preterm infants are prone to gastrointestinal complications such as infectious diseases and necrotizing enterocolitis, which are associated with intestinal inflammation and increased intestinal permeability. Intestinal epithelial barrier (IEB) function is known to be immature in preterm neonates; however, our understanding of how the IEB develops - particularly the formation of junctional complexes - remains limited. Here, we analyzed intestinal tissue specimens from healthy resection margins of six very immature preterm infants who underwent bowel resection due to focal intestinal perforation (at the chronological age of 25 to 28 weeks' gestation), and compared the composition of tight junctions, adherens junctions and desmosomes to that of adults. Using immunostaining, our observations show, that tight junction proteins Claudin-2, Claudin-3 and Occludin, adherens junction proteins E-cadherin and β-Catenin as well as desmosomal proteins Plakoglobin and Plakophilin-2 appeared as mature as in adults as early as 25 weeks' gestation. However, Claudin-1, -4 and -5, as well as ZO-1 staining patterns increased and became more defined with increasing gestational age, suggesting junctional maturation during gestational week 26 and 27. Desmosomal protein Desmocollin-2 was increased until 26 weeks' gestation whereas Desmoglein-2 and Desmoplakin expression was immature at 28 weeks' gestation compared to the expression in adults. Our study provides the first sequential characterization of junctional protein maturation across all major IEB components early in life in human samples. These findings may help identify key mechanisms underlying intestinal barrier-associated pathologies in preterm infants.
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