2017Annals of the New York Academy of SciencesOpen access

Site‐specific distribution of claudin‐based paracellular channels with roles in biological fluid flow and metabolism

Hiroo Tanaka, Atsushi Tamura, Koya Suzuki, Sachiko Tsukita

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Abstract

Abstract The claudins are a family of membrane proteins with at least 27 members in humans and mice. The extracellular regions of claudin proteins play essential roles in cell–cell adhesion and the paracellular barrier functions of tight junctions (TJs) in epithelial cell sheets. Furthermore, the extracellular regions of some claudins function as paracellular channels in the paracellular barrier that allow the selective passage of water, ions, and/or small organic solutes across the TJ in the extracellular space. Structural analyses have revealed a common framework of transmembrane, cytoplasmic, and extracellular regions among the claudin‐based paracellular barriers and paracellular channels; however, differences in the claudins’ extracellular regions, such as their charges and conformations, determine their properties. Among the biological systems that involve fluid flow and metabolism, it is noted that hepatic bile flow, renal Na+reabsorption, and intestinal nutrient absorption are dynamically regulated via site‐specific distributions of paracellular channel–forming claudins in tissue. Here, we focus on how site‐specific distributions of claudin‐2– and claudin‐15–based paracellular channels drive their organ‐specific functions in the liver, kidney, and intestine.

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Abstract The claudins are a family of membrane proteins with at least 27 members in humans and mice. The extracellular regions of claudin proteins play essential roles in cell–cell adhesion and the paracellular barrier functions of tight junctions (TJs) in epithelial cell sheets. Furthermore, the extracellular regions of some claudins function as paracellular channels in the paracellular barrier that allow the selective passage of water, ions, and/or small organic solutes across the TJ in the extracellular space. Structural analyses have revealed a common framework of transmembrane, cytoplasmic, and extracellular regions among the claudin‐based paracellular barriers and paracellular channels; however, differences in the claudins’ extracellular regions, such as their charges and conformations, determine their properties. Among the biological systems that involve fluid flow and metabolism, it is noted that hepatic bile flow, renal Na+reabsorption, and intestinal nutrient absorption are dynamically regulated via site‐specific distributions of paracellular channel–forming claudins in tissue. Here, we focus on how site‐specific distributions of claudin‐2– and claudin‐15–based paracellular channels drive their organ‐specific functions in the liver, kidney, and intestine.

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Available abstract

Abstract The claudins are a family of membrane proteins with at least 27 members in humans and mice. The extracellular regions of claudin proteins play essential roles in cell–cell adhesion and the paracellular barrier functions of tight junctions (TJs) in epithelial cell sheets. Furthermore, the extracellular regions of some claudins function as paracellular channels in the paracellular barrier that allow the selective passage of water, ions, and/or small organic solutes across the TJ in the extracellular space. Structural analyses have revealed a common framework of transmembrane, cytoplasmic, and extracellular regions among the claudin‐based paracellular barriers and paracellular channels; however, differences in the claudins’ extracellular regions, such as their charges and conformations, determine their properties. Among the biological systems that involve fluid flow and metabolism, it is noted that hepatic bile flow, renal Na+reabsorption, and intestinal nutrient absorption are dynamically regulated via site‐specific distributions of paracellular channel–forming claudins in tissue. Here, we focus on how site‐specific distributions of claudin‐2– and claudin‐15–based paracellular channels drive their organ‐specific functions in the liver, kidney, and intestine.

Key concepts: Paracellular transport, Claudin, Extracellular, Tight junction, Cell biology, Transcellular, Reabsorption, Chemistry

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