The effect of claudin-15 deletion on cationic selectivity and transport in paracellular pathways of the cecum and large intestine

• Published in: Scientific reports Vol. 13; no. 1; p. 6799
• Main Authors: Hempstock, Wendy, Nagata, Nozomi, Ishizuka, Noriko, Hayashi, Hisayoshi
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 26.04.2023; Nature Publishing Group; Nature Portfolio
• Subjects: 631/443; 692/4020; Animals; Cations - metabolism; Cecum; Cecum - metabolism; Claudins - genetics; Claudins - metabolism; Electrical resistivity; Electrolyte balance; Fatty acids; Humanities and Social Sciences; Ion Transport; Ions; Large intestine; Mice; Molecular modelling; multidisciplinary; Permeability; Physiology; Science; Science (multidisciplinary); Short-circuit current; Small intestine; Sodium conductance; Tight junctions; Tight Junctions - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-023-33431-5

The large intestine plays a pivotal role in water and electrolyte balance. Paracellular transport may play a role in ion transport mechanisms in the cecum and large intestine; however, these molecular mechanisms and their physiological roles have not been fully studied. Claudin-15 forms a cation channel in tight junctions in the small intestine, but its role in the cecum and large intestine has not been investigated. This study aimed to explore the physiological role of claudin-15 in the cecum and large intestine using claudin-15 (Cldn15) KO mice. Electrical conductance, short-circuit current, Na + flux, and dilution potential were assessed in isolated tissue preparations mounted in Ussing chambers. The induced short-circuit current of short-chain fatty acids, which are fermentative products in the intestinal tract, was also measured. Compared to wild type mice, the electrical conductance and paracellular Na + flux was decreased in the cecum, but not the middle large intestine, while in both the cecum and the middle large intestine, paracellular Na + permeability was decreased in Cldn15 KO mice. These results suggest that claudin-15 is responsible for Na + permeability in the tight junctions of the cecum and large intestine and decreased Na + permeability in the cecum may cause impaired absorption function.