首页> 外文期刊>American Journal of Physiology >Protein tyrosine kinase is expressed and regulates ROMK1 location in the cortical collecting duct.
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Protein tyrosine kinase is expressed and regulates ROMK1 location in the cortical collecting duct.

机译:蛋白酪氨酸激酶被表达并调节ROMK1在皮层收集管中的位置。

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摘要

We previously demonstrated that dietary K intake regulates the expression of Src family PTK, which plays an important role in controlling the expression of ROMK1 in plasma membrane (Wei Y, Bloom P, Lin D-H, Gu RM, and Wang WH. Am J Physiol Renal Physiol 281: F206-F212, 2001). In the present study, we used the immunofluorescence staining technique to demonstrate the presence of c-Src, a member of Src family PTK, in the thick ascending limb (TAL) and collecting duct. Confocal microscopy shows that c-Src is highly expressed in the renal cortex and outer medulla. Moreover, c-Src and ROMK are coexpressed in the same nephron segment. Also, the positive staining of c-Src is visible in tubules stained with Tamm-Horsfall glycoprotein or aquaporin-2. This suggests that c-Src is present in the TAL, cortical collecting duct (CCD), and outer medullary collecting duct (OMCD). To study the role of PTK in the regulation of ROMK membrane expression in the TAL and CCD, we carried out immunocytochemical staining with ROMK antibody in the CCD or TAL from rats on either a high-K (HK) or K-deficient (KD) diet. A sharp membrane staining of ROMK can be observed in the TAL from rats on both HK and KD diets. However, a clear plasma membrane staining can be observed only in the CCD from rats on a HK diet but not from those on a KD diet. Treatment of the CCD from rats on a HK diet with phenylarsine oxide (PAO) decreases the positive staining in the plasma/subapical membrane and increases the ROMK staining in the intracellular compartment. However, PAO treatment did not significantly alter the staining pattern of ROMK in the TAL. Moreover, the biotinylation technique has also confirmed that neither herbimycin A nor PAO has significantly changed the biotin-labeled ROMK2 in HEK293 cells transfected with ROMK2 and c-Src. We conclude that c-Src is expressed in the TAL, CCD, and OMCD and that stimulation of PTK increases the ROMK channels in the intracellular compartment but decreases them in the apical/subapical membrane in the CCD.
机译:我们先前证明饮食中的钾摄入量可调节Src家族PTK的表达,这在控制质膜ROMK1的表达中起着重要作用(Wei Y,Bloom P,Lin DH,Gu RM和Wang WH。Am J Physiol Renal生理学281:F206-F212,2001)。在本研究中,我们使用免疫荧光染色技术来证明c-Src(Src家族PTK的成员)存在于粗大上升肢体(TAL)和收集管中。共聚焦显微镜检查显示,c-Src在肾皮质和髓质外高表达。此外,c-Src和ROMK在同一肾单位段中共表达。同样,在用Tamm-Horsfall糖蛋白或aquaporin-2染色的小管中可见c-Src的阳性染色。这表明c-Src存在于TAL,皮质收集管(CCD)和髓外收集管(OMCD)中。为了研究PTK在TAL和CCD中ROMK膜表达的调节中的作用,我们在高K(HK)或K缺乏(KD)大鼠上用CCD或TAL中的ROMK抗体进行了免疫细胞化学染色饮食。在使用HK和KD饮食的大鼠中,TAL的ROMK膜均清晰可见。但是,仅在使用HK饮食的老鼠的CCD中可以观察到清晰的质膜染色,而使用KD饮食的老鼠的CCD则看不到。在HK饮食下用苯the氧化物(PAO)处理大鼠的CCD,可减少质膜/根尖膜的阳性染色,并增加细胞内区室的ROMK染色。但是,PAO处理并未显着改变TAL中ROMK的染色模式。此外,生物素化技术还证实除草霉素A和PAO均未显着改变转染ROMK2和c-Src的HEK293细胞中生物素标记的ROMK2。我们得出的结论是,c-Src在TAL,CCD和OMCD中表达,并且PTK的刺激增加了细胞内区室中的ROMK通道,但在CCD的顶/近根膜中减少了它们。

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