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Updated: May 5, 2026

In Vitro and In Vivo Approaches to Determine Intestinal Epithelial Cell Permeability
Published on: October 19, 2018
Curcumin prevents leptin-induced tight junction dysfunction in intestinal Caco-2 BBe cells
Choon Young Kim1, Kee-Hong Kim
1Department of Food Science, Purdue University, West Lafayette, IN 47907, USA.
Luminal leptin disrupts intestinal barrier function by activating signaling pathways, leading to inflammation. Curcumin (CCM) pretreatment prevents this leptin-induced tight junction (TJ) dysfunction in intestinal cells.
Area of Science:
- Gastroenterology
- Cell Biology
- Immunology
Background:
- Intestinal tight junction (TJ) integrity is vital for nutrient absorption, host defense, and immunity.
- Leptin, linked to obesity and intestinal inflammation, has an unclear role in luminal TJ function.
Purpose of the Study:
- To investigate leptin's role in intestinal TJ function in Caco-2 BBe cells.
- To explore curcumin's (CCM) protective effects against leptin-induced TJ dysfunction.
Main Methods:
- Treated Caco-2 BBe cells with apical leptin and/or curcumin (CCM).
- Analyzed TJ function, signaling pathways (JAK2/STAT3, PI3K/Akt/ERK1/2), and gene expression (TJ proteins, IL-6, TNF-α).
Main Results:
- Apical leptin (100 ng/ml) impaired TJ function by activating leptin receptor-dependent JAK2/STAT3 and PI3K/Akt/ERK1/2 pathways.
- Leptin reduced TJ-associated proteins (zonula occludens-3, claudin-5, occludin) and increased inflammatory genes (IL-6, TNF-α).
- CCM pretreatment blunted leptin's effects by inhibiting these signaling pathways and gene expression changes.
Conclusions:
- Luminal leptin novelly impairs intestinal TJ function via specific signaling pathways.
- Curcumin (CCM) effectively prevents leptin-induced TJ dysfunction in intestinal cells, highlighting its potential therapeutic role.
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