Caco2/HT-29 In Vitro Cell Co-Culture: Barrier Integrity, Permeability, and Tight Junctions’ Composition During Progressive Passages of Parental Cells
Articolo
Data di Pubblicazione:
2025
Citazione:
Caco2/HT-29 In Vitro Cell Co-Culture: Barrier Integrity, Permeability, and Tight Junctions’ Composition During Progressive Passages of Parental Cells / E. Donetti, P. Bendinelli, M. Correnti, E. Gammella, S. Recalcati, A. Ferraretto. - In: BIOLOGY. - ISSN 2079-7737. - 14:3(2025 Mar 06), pp. 267.1-267.16. [10.3390/biology14030267]
Abstract:
Epithelial linings are crucial for the maintenance of physiological barriers. The intestinal epithelial barrier (IEB) consists of enterocytes through tight junctions and mucus-secreting cells and can undergo physiological modifications throughout life. To reproduce as closely as possible the IEB main features over time, in vitro co-cultures of Caco2/HT-29 70/30 formed by parental Caco2 and HT-29 cells sub-cultivated for more than 40 passages were set up. The measurements of the transepithelial electrical resistance (TEER) identified two populations: physiological TEER co-cultures (PC) with values > 50 Ωcm2 formed by parental cells with fewer than 40 passages, and leaky TEER co-cultures (LC) with values < 50 Ωcm2 formed by parental cells with more than 40 passages. In LC, paracellular permeability increased in parallel. By immunofluorescence and Western blot analysis, an increase in claudin 2 was observed in LC vs. PC, with no differences in occludin expression. MUC-2 immunoreactivity was stronger in PC than in LC. LC also showed an enhanced vulnerability to TNFα+IFN-γ. These results reproduce the main morpho-functional modifications reported in the human leaky/aged gut and support the usefulness of our in vitro cell model for studying the molecular processes underlying these modifications and testing drug/nutraceutical treatments to ameliorate leaky gut aging.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
intestinal epithelial barrier; transepithelial electrical resistance; claudin 2; occludin; MUC-2; co-culture; western blot; transmission electron microscopy; immunofluorescence;
Elenco autori:
E. Donetti, P. Bendinelli, M. Correnti, E. Gammella, S. Recalcati, A. Ferraretto
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