Singh Richa, Kursan Shams, Almiahoub Mohamed Y, Almutairi Mohammed M, Garzón-Muvdi Tomás, Alvarez-Leefmans Francisco J, Di Fulvio Mauricio
Department of Pharmacology and Toxicology, Boonshoft School of Medicine, Wright State University Dayton, OH, USA.
Front Cell Dev Biol. 2017 Jan 4;4:150. doi: 10.3389/fcell.2016.00150. eCollection 2016.
NaK2Cl co-transporters (NKCCs) effect the electroneutral movement of Na-K and 2Cl ions across the plasma membrane of vertebrate cells. There are two known NKCC isoforms, NKCC1 () and NKCC2 (). NKCC1 is a ubiquitously expressed transporter involved in cell volume regulation, Cl homeostasis and epithelial salt secretion, whereas NKCC2 is abundantly expressed in kidney epithelial cells of the thick ascending loop of Henle, where it plays key roles in NaCl reabsorption and electrolyte homeostasis. Although NKCC1 and NKCC2 co-transport the same ions with identical stoichiometry, NKCC1 actively co-transports water whereas NKCC2 does not. There is growing evidence showing that NKCC2 is expressed outside the kidney, but its function in extra-renal tissues remains unknown. The present study shows molecular and functional evidence of endogenous NKCC2 expression in COS7 cells, a widely used mammalian cell model. Endogenous NKCC2 is primarily found in recycling endosomes, Golgi cisternae, Golgi-derived vesicles, and to a lesser extent in the endoplasmic reticulum. Unlike NKCC1, NKCC2 is minimally hybrid/complex N-glycosylated under basal conditions and yet it is trafficked to the plasma membrane region of hyper-osmotically challenged cells through mechanisms that require minimal complex N-glycosylation or functional Golgi cisternae. Control COS7 cells exposed to slightly hyperosmotic (~6.7%) solutions for 16 h were not shrunken, suggesting that either one or both NKCC1 and NKCC2 may participate in cell volume recovery. However, NKCC2 targeted to the plasma membrane region or transient over-expression of NKCC2 failed to rescue NKCC1 in COS7 cells where NKCC1 had been silenced. Further, COS7 cells in which NKCC1, but not NKCC2, was silenced exhibited reduced cell size compared to control cells. Altogether, these results suggest that NKCC2 does not participate in cell volume recovery and therefore, NKCC1 and NKCC2 are functionally different NaK2Cl co-transporters.
钠钾氯协同转运蛋白(NKCCs)介导钠、钾和两个氯离子在脊椎动物细胞膜上的电中性转运。已知有两种NKCC亚型,即NKCC1( )和NKCC2( )。NKCC1是一种广泛表达的转运蛋白,参与细胞体积调节、氯离子稳态及上皮细胞盐分分泌,而NKCC2在髓袢升支粗段肾上皮细胞中大量表达,在氯化钠重吸收和电解质稳态中起关键作用。尽管NKCC1和NKCC2以相同的化学计量协同转运相同离子,但NKCC1能主动协同转运水,而NKCC2则不能。越来越多的证据表明NKCC2在肾脏外也有表达,但其在肾外组织中的功能尚不清楚。本研究展示了在广泛应用的哺乳动物细胞模型COS7细胞中内源性NKCC2表达的分子及功能证据。内源性NKCC2主要存在于循环内体、高尔基池、高尔基衍生的囊泡中,在内质网中含量较少。与NKCC1不同,NKCC2在基础条件下极少发生杂合/复杂N-糖基化,但它可通过需要极少复杂N-糖基化或功能性高尔基池的机制转运至高渗刺激细胞的质膜区域。暴露于轻度高渗(约6.7%)溶液16小时的对照COS7细胞未发生皱缩,这表明NKCC1和NKCC2中的一个或两者可能参与细胞体积恢复。然而,靶向质膜区域或瞬时过表达NKCC2均无法挽救COS7细胞中已沉默的NKCC1。此外,与对照细胞相比,沉默NKCC1而非NKCC2的COS7细胞尺寸减小。总之,这些结果表明NKCC2不参与细胞体积恢复,因此,NKCC1和NKCC2是功能不同的钠钾氯协同转运蛋白。