Angulin-2/ILDR1, a tricellular tight junction protein, does not affect water transport in the mouse large intestine

• Published in: Scientific reports Vol. 10; no. 1; p. 10374
• Main Authors: Hempstock, Wendy, Sugioka, Shiori, Ishizuka, Noriko, Sugawara, Taichi, Furuse, Mikio, Hayashi, Hisayoshi
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 25.06.2020; Nature Publishing Group
• Subjects: 631/443; 692/4020; Animals; Biological Transport; Colon; Colon - metabolism; Deafness; Epithelial Cells - metabolism; Humanities and Social Sciences; Kidneys; Large intestine; Localization; Male; Mice; Mice, Knockout; multidisciplinary; Permeability; Phenotypes; Proteins; Receptors, Cell Surface - physiology; Rodents; Science; Science (multidisciplinary); Tight junctions; Tight Junctions - physiology; Water - metabolism; Water transport
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-67319-5

Angulin-2/ILDR1 is a member of the angulin protein family, which is exclusively expressed at tricellular tight junctions in epithelia. Tricellular tight junctions are found where three cells meet and where three bicellular tight junction strands converge. Tricellular tight junctions are thought to be important for paracellular permeability of ions and water in epithelial tissues. It was recently reported that angulin-2/ILDR1 knockout mice have water transport abnormalities in the kidney. Since angulin-2/ILDR1 is the main tricellular tight junction protein in the large intestine, the goal of this research was to examine the effect of angulin-2/ILDR1 knockout on large intestinal paracellular water transport. We found that Ildr1 knockout mice showed no detectable phenotype other than deafness. In addition, paracellular transport as assessed by Ussing chamber was unchanged in Ildr1 knockout mice. However, we found that in the colon and the kidney of Ildr1 knockout mice, another tricellular tight junction protein, angulin-1/LSR, changes its expression pattern. We propose that with this replacement in tissue localization, angulin-1/LSR compensates for the loss of angulin-2/ILDR1 and maintains the barrier and function of the epithelia in the large intestine as well as the kidney.