首页> 外文期刊>Cellular Physiology and Biochemistry >Dopamine D-1-like receptor-mediated inhibition of Cl-/HCO3- exchanger activity in rat intestinal epithelial IEC-6 cells is regulated by G protein-coupled receptor kinase 6 (GRK 6)
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Dopamine D-1-like receptor-mediated inhibition of Cl-/HCO3- exchanger activity in rat intestinal epithelial IEC-6 cells is regulated by G protein-coupled receptor kinase 6 (GRK 6)

机译:G蛋白偶联受体激酶6(GRK 6)调节多巴胺D-1样受体介导的大鼠肠上皮IEC-6细胞对Cl- / HCO3-交换子活性的抑制

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The present study investigated the effect of dopamine D-1-like receptor stimulation on the Cl-/HCO3- exchange activity in rat intestinal epithelial IEC-6 cells. The Cl-/ HCO3-exchange activity was found to be a chloride-dependent, DIDS-sensitive and niflumate-insensitive process. The presence of the SLC26A6 anion exchanger was detected by both RT-PCR and immunoblotting analysis in IEC-6 cells, in which three different small interfering RNAs (siRNAs) targeting SLC26A6 markedly inhibited Cl-/HCO3(-) exchange. Activation of dopamine D-1-like receptors with SKF 38393 inhibited Cl-/HCO3- exchanger activity, this being antagonized by the D 1 selective antagonist SKF 83566. However, effects of SKF 38393 were maximal at 5 min of exposure to the agonist and rapidly diminished with no effect at 15 min, suggestive of agonist-induced desensitization of D-1-like receptors. Pretreatment of cells with heparin, a non-selective inhibitor of G protein-coupled receptor kinases (GRKs), prevented the observed attenuation of SKF 38393-induced inhibition of Cl-/HCO3- exchange. Overnight pretreatment with anti-GRK6A and antiGRK6B, but not with anti-GRK4 antibodies, prevented the loss of SKF 38393-mediated effects. Both PKA and PKC signaling pathways participate in SKF 38393-mediated inhibition of Cl-/HCO3- exchange. These findings suggest that SLC26A6 is at least one of the anion exchanger's family members responsible for Cl-/HCO3- exchange in IEC-6 cells. Dopamine D-1 receptors in IEC-6 rapidly desensitize to D-1-like agonist stimulation and GRK 6, but not GRK 4, appear to be involved in agonist-mediated responsiveness and desensitization.
机译:本研究调查了多巴胺D-1样受体刺激对大鼠肠上皮IEC-6细胞Cl- / HCO3-交换活性的影响。发现Cl- / HCO3-交换活性是氯化物依赖性的,对DIDS敏感的和对氟甲酸酯不敏感的过程。通过RT-PCR和免疫印迹分析在IEC-6细胞中检测到SLC26A6阴离子交换剂的存在,其中靶向SLC26A6的三种不同的小干扰RNA(siRNA)明显抑制了Cl- / HCO3(-)交换。用SKF 38393激活多巴胺D-1-like受体抑制了Cl- / HCO3-交换子活性,这被D 1选择性拮抗剂SKF 83566拮抗。但是,SKF 38393在暴露于激动剂5分钟后效果最大。迅速消失,在15分钟时没有影响,提示激动剂引起的D-1-like受体脱敏。肝素预处理细胞是一种非选择性的G蛋白偶联受体激酶(GRKs)抑制剂,可防止观察到的SKF 38393诱导的Cl- / HCO3-交换抑制作用减弱。使用抗GRK6A和抗GRK6B进行过夜预处理,但未使用抗GRK4抗体进行预处理,可以防止SKF 38393介导的作用丧失。 PKA和PKC信号通路均参与SKF 38393介导的Cl- / HCO3-交换抑制。这些发现表明,SLC26A6是负责IEC-6细胞中Cl- / HCO3-交换的阴离子交换剂家族成员中的至少一个。 IEC-6中的多巴胺D-1受体对D-1样激动剂刺激迅速脱敏,而GRK 6(而非GRK 4)似乎与激动剂介导的反应性和脱敏有关。

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