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Endogenous ATP release inhibits electrogenic Na+ absorption and stimulates Cl? secretion in MDCK cells

机译:内源性ATP释放抑制MDCK细胞中电致Na +吸收并刺激Cl?分泌

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Our previous studies with a line of Madin-Darby canine kidney (MDCK) cells (FL-MDCK) transfected with FLAG-labeled α, β, and γ subunits of epithelial Na+ channel (ENaC) showed that, although most of the short-circuit current (I sc) was amiloride sensitive (AS-I sc), there was also an amiloride-insensitive component (NS-I sc) due to Cl? secretion (Morris and Schafer, J Gen Physiol 120:71–85, 2002). In the present studies, we observed a progressive increase in NS-I sc and a corresponding decrease in AS-I sc during experiments. There was a significant negative correlation between AS-I sc and NS-I sc both in the presence and absence of treatment with cyclic adenosine monophosphate (cAMP). NS-I sc could be attributed to both cystic fibrosis transmembrane conductance regulator (CFTR) and a 4, 4'-diisothiocyano-2, 2'-disulfonic acid stilbene (DIDS)-sensitive Ca2+-activated Cl? channel (CaCC). Continuous perfusion of both sides of the Ussing chamber with fresh rather than recirculated bathing solutions, or addition of hexokinase (6 U/ml), prevented the time-dependent changes and increased AS-I sc by 40–60%, with a proportional decrease in NS-I sc. Addition of 100 μM adenosine triphosphate (ATP) in the presence of luminal amiloride produced a transient four-fold increase in NS-I sc that was followed by a sustained increase of 50–60% above the basal level. ATP release from the monolayers, measured by bioluminescence, was found to occur across the apical but not the basolateral membrane, and the apical release was tripled by cAMP treatment. These data show that constitutive apical ATP release, which occurs under both basal and cAMP-stimulated conditions, underlies the time-dependent rise in Cl? secretion and the proportional fall in ENaC-mediated Na+ absorption in FL-MDCK cells. Thus, endogenous ATP release can introduce a significant confounding variable in experiments with this and similar epithelial cells, and it may underlie at least some of the observed interaction between Cl? secretion and Na+ absorption.
机译:我们之前对一系列用FLAG标记的上皮Na +通道的α,β和γ亚基转染的Madin-Darby犬肾(MDCK)细胞(FL-MDCK)进行的研究表明,尽管大多数短路电流(I sc )是对阿米洛利敏感的(AS-I sc ),还有一个由于Cl?< / sup>分泌(Morris and Schafer,J Gen Physiol 120:71–85,2002)。在本研究中,我们观察到在实验过程中NS-I sc 逐渐增加,而AS-I sc 相应减少。无论有无环磷酸腺苷(cAMP)治疗,AS-I sc 和NS-I sc 之间均存在显着的负相关。 NS-1sc 既可以归因于囊性纤维化跨膜电导调节剂(CFTR),也可以归因于4、4'-二异硫氰基-2、2'-二磺酸(DIDS)敏感的Ca2 +激活。 Cl?通道(CaCC)。用新鲜的而不是循环的沐浴液持续向Ussing室的两侧进行灌注,或者添加己糖激酶(6 U / ml),可以防止时间依赖性变化,并使AS-I sc 升高40-60%, NS-I sc 呈比例下降。在阿米洛利腔内存在的情况下,添加100μM三磷酸腺苷(ATP)可使NS-I sc 瞬时增加4倍,随后持续比基础水平持续增加50–60%。发现通过生物发光测量的单层ATP释放发生在整个顶膜,而不是在基底外侧膜,并且通过cAMP处理使顶膜释放增加了两倍。这些数据表明,在基础和cAMP刺激条件下均发生本构性心尖ATP释放,这是Cl?分泌随时间变化的上升和FL中ENaC介导的Na + 吸收成比例下降的基础。 -MDCK细胞。因此,内源性ATP释放可以在与该上皮细胞和类似上皮细胞的实验中引入一个显着的混杂变量,并且可能是所观察到的至少部分Cl +分泌与Na +吸收之间相互作用的基础。

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