Yu Alan S L
a Division of Nephrology and Hypertension, Department of Internal Medicine , University of Kansas Medical Center , Kansas City , KS , USA.
b Division of Infectious Diseases, Department of Internal Medicine , University of Kansas Medical Center , Kansas City , KS , USA.
Tissue Barriers. 2017 Apr 3;5(2):e1301852. doi: 10.1080/21688370.2017.1301852. Epub 2017 Mar 3.
Paracellular transport of solutes and water accompanies transcellular transport across epithelial barriers and together they serve to maintain internal body composition. However, whether paracellular transport is necessary and why it evolved is unknown. In this commentary I discuss our recent studies to address this question in the proximal tubule of the kidney. Paracellular reabsorption of sodium occurs in the proximal tubule and is mediated by claudin-2. However, deletion of claudin-2 in mice does not affect whole kidney sodium excretion because it can be completely compensated by downtream transcellular transport mechanisms. This occurs at the expense of increased oxygen consumption, tissue hypoxia and increased susceptibility to ischemic injury. It is concluded that paracellular transport acts as an energy saving mechanism to increase transport without consuming additional oxygen. It is speculated that this might be why paracellular transport evolved in leaky epithelia with high transport needs.
溶质和水的细胞旁转运伴随着跨上皮屏障的跨细胞转运,二者共同作用以维持体内成分。然而,细胞旁转运是否必要以及其进化的原因尚不清楚。在这篇评论中,我将讨论我们最近为解决肾脏近端小管中的这个问题所开展的研究。近端小管中存在钠的细胞旁重吸收,其由claudin-2介导。然而,小鼠中claudin-2的缺失并不影响全肾钠排泄,因为它可被下游的跨细胞转运机制完全代偿。这是以增加氧气消耗、组织缺氧以及对缺血性损伤易感性增加为代价的。结论是,细胞旁转运作为一种节能机制,可在不消耗额外氧气的情况下增加转运。据推测,这可能就是细胞旁转运在具有高转运需求的渗漏上皮中进化的原因。