首页> 外文期刊>Journal of cellular biochemistry. >Interferon-gamma suppresses Na+ -H+ exchanger in cultured human endolymphatic sac epithelial cells.
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Interferon-gamma suppresses Na+ -H+ exchanger in cultured human endolymphatic sac epithelial cells.

机译:干扰素-γ抑制培养的人内淋巴囊上皮细胞中的Na + -H +交换子。

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摘要

Adequate regulation of endolymphatic pH is essential for maintaining inner ear function. The Na(+)-H(+) exchanger (NHE) is a major determinant of intracellular pH (pH(i)), and facilitates Na(+) and fluid absorption in various epithelia. We determined the functional and molecular expression of NHEs in cultured human endolymphatic sac (ES) epithelial cells and examined the effect of IFN-gamma on NHE function. Serial cultures of human ES epithelial cells were generated from tissue samples. The molecular expression of NHE1, -2, and -3 isoforms was determined by real-time RT-PCR. The functional activity of NHE isoforms was measured microfluorometrically using a pH-sensitive fluorescent dye, 2',7'-bis(carbonylethyl)-5(6)-carboxyfluorescein (BCECF), and a NHE-inhibitor, 3-methylsulfonyl-4-piperidinobenzoyl guanidine methanesulfonate (HOE694). NHE1, -2, and -3 mRNAs were expressed in human ES epithelial cells. Functional activity of NHE1 and -2 was confirmed in the luminal membrane of ES epithelial cells by sequentially suppressing Na(+)-dependent pH(i) recovery from intracellular acidification using different concentrations of HOE694. Treatment with IFN-gamma (50 nM for 24 h) suppressed mRNA expression of NHE1 and -2. IFN-gamma also suppressed functional activity of both NHE1 and -2 in the luminal membrane of ES epithelial cells. This study shows that NHEs are expressed in cultured human ES epithelial cells and that treatment with IFN-gamma suppresses the expression and functional activity of NHE1 and -2.
机译:充分调节内淋巴的pH值对于维持内耳功能至关重要。 Na(+)-H(+)交换剂(NHE)是细胞内pH(pH(i))的主要决定因素,并促进Na(+)和液体在各种上皮细胞中的吸收。我们确定了培养的人内淋巴囊(ES)上皮细胞中NHE的功能和分子表达,并检查了IFN-γ对NHE功能的影响。人ES上皮细胞的系列培养物是从组织样品中产生的。通过实时RT-PCR确定NHE1,-2和-3同工型的分子表达。使用pH敏感的荧光染料2',7'-双(羰基乙基)-5(6)-羧基荧光素(BCECF)和NHE抑制剂3-甲基磺酰基-4-微荧光法测量NHE亚型的功能活性哌啶子基苯甲酰胍甲磺酸盐(HOE694)。 NHE1,-2和-3 mRNA在人ES上皮细胞中表达。通过使用不同浓度的HOE694从细胞内酸化中依次抑制Na(+)-依赖的pH(i)恢复,可以在ES上皮细胞腔膜中确认NHE1和-2的功能活性。 IFN-γ处理(50 nM,持续24 h)可抑制NHE1和-2的mRNA表达。 IFN-γ还抑制了ES上皮细胞腔膜中NHE1和-2的功能活性。这项研究表明,NHE在培养的人ES上皮细胞中表达,并且用IFN-γ处理会抑制NHE1和-2的表达和功能活性。

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