| Literature DB >> 26729464 |
Hiroo Tanaka1, Yasuko Yamamoto2, Hiroka Kashihara1, Yuji Yamazaki3, Kazutoshi Tani4, Yoshinori Fujiyoshi5, Katsuhiko Mineta6, Kosei Takeuchi7, Atsushi Tamura8, Sachiko Tsukita8.
Abstract
Claudin protein family members, of which there are at least 27 in humans and mice, polymerize to form tight junctions (TJs) between epithelial cells, in a tissue- and developmental stage-specific manner. Claudins have a paracellular barrier function. In addition, certain claudins function as paracellular channels for small ions and/or solutes by forming selective pores at the TJs, although the specific claudins involved and their functional mechanisms are still in question. Here we show for the first time that claudin-21, which is more highly expressed in the embryonic than the postnatal stages, acts as a paracellular channel for small cations, such as Na(+), similar to the typical channel-type claudins claudin-2 and -15. Claudin-21 also allows the paracellular passage of larger solutes. Our findings suggest that claudin-21-based TJs allow the passage of small and larger solutes by both paracellular channel-based and some additional mechanisms.Entities:
Mesh:
Substances:
Year: 2016 PMID: 26729464 PMCID: PMC4810463 DOI: 10.1128/MCB.00758-15
Source DB: PubMed Journal: Mol Cell Biol ISSN: 0270-7306 Impact factor: 4.272