Heterogeneity of tight junctions in the thick ascending limb

被引:13
作者
Bleich, Markus [1 ]
Wulfmeyer, Vera C. [1 ,2 ]
Himmerkus, Nina [1 ]
Milatz, Susanne [1 ]
机构
[1] Univ Kiel, Inst Physiol, Kiel, Germany
[2] Hannover Med Sch, Dept Nephrol & Hypertens, Hannover, Germany
关键词
claudin; calcium; magnesium; epithelial transport; nephrocalcinosis; CALCIUM-SENSING RECEPTOR; ACTIVE NACL TRANSPORT; HENLES LOOP; RABBIT KIDNEY; PARATHYROID-HORMONE; PARACELLULAR NA+; MG2+ TRANSPORT; PERMEABILITY; CLAUDIN-16; MOUSE;
D O I
10.1111/nyas.13400
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Renal tubular transport mechanisms are optimized to be energy efficient and tailored to local gradients and transport rates. The combined transcellular action of ion channels, transporters, and pumps, together with the paracellular pathway, enables kidney function. Monogenetic diseases and mouse models indicate that both trans- and paracellular proteins can become disease-causing candidates and may be targets for future therapeutic approaches. Recent advances in tight junction research have provided new insights into their structure, function, and regulation. The thick ascending limb (TAL) is a nephron segment with specific requirements for the paracellular pathway. It has to fuel the generation of the corticomedullary concentration gradient, to be watertight, and to provide a highly selective permeability for Na+ and divalent cations. Tight junction composition and function in the TAL is organized along the corticomedullary axis. Even on the level of a seemingly homogeneous tubular epithelium like the TAL, there is a separation of tight junction protein expression in the strands between the respective tricellular nexus of the junctional network. Here, we highlight some new insights from our recent work and that of others in this context. In addition, we provide some perspectives for the further study of paracellular transport mechanisms.
引用
收藏
页码:5 / 15
页数:11
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