کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2529913 | 1558129 | 2014 | 6 صفحه PDF | دانلود رایگان |
• Paracellular flux is regulated by dynamic tight junction protein interactions.
• Claudin interactions define small molecule flux across tight junction pores.
• Macromolecular flux occurs via the non-selective tight junction leak pathway.
• Pore and leak pathways are differentially regulated in health and disease.
In complex multicellular organisms, epithelia lining body cavities regulate absorption and secretion of ions, organic molecules, and water. Proper function of epithelia depends on apically and basolaterally situated ion channels as well as tight junctions which seal the apical intercellular space. Without tight junctions, transepithelial concentration gradients of ions and nutrients would be dissipated through the paracellular space. Elevated tight junction permeability is a feature of many diseases of multiple organs, including the gastrointestinal tract [1, 2, 3
• and 4
• ], kidney [5 and 6], and lungs [7 and 8]. In the intestines, epithelial barrier dysfunction is a major contributor to diarrhea and malnutrition and is associated with significant morbidity and mortality worldwide.
Journal: Current Opinion in Pharmacology - Volume 19, December 2014, Pages 84–89