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大鼠输出小管和附睾尾部培养上皮细胞中多种钠氢交换体亚型的表达

Expression of multiple Na+/H+ exchanger isoforms in cultured epithelial cells from rat efferent duct and cauda epididymidis.

作者信息

Leung G P, Tse C M, Chew S B, Wong P Y

机构信息

Department of Physiology, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.

出版信息

Biol Reprod. 2001 Feb;64(2):482-90. doi: 10.1095/biolreprod64.2.482.

Abstract

Although earlier work has pointed to the presence of Na+/H+ exchangers (NHEs) in the rat epididymis, little is known about the regional distribution of various NHE isoforms and their functions. In the present work, expression of different isoforms of NHE in cultured epithelia of the efferent duct and cauda epdidymidis were studied. Reverse transcription-polymerase chain reaction revealed the presence of NHE1, NHE2, and NHE3, but not NHE4, message in both cultured epithelia. Western blot analysis detected the presence of NHE1 and NHE2 proteins in both cultured epithelia, but NHE3 protein was only detected in the cultured epithelial cells from the efferent duct. Immunohistochemical studies demonstrated that NHE2 was localized in the cytoplasm of the ciliated cells, whereas NHE3 was localized at the apical membrane of the principal cells of the efferent duct. The NHE activities in both cultured epithelia were inhibited by 10 microM HOE-694 (3-methylsulphonyl-4-piperidinobenzoyl guanidine methanesulphonate), a NHE1 inhibitor, by approximately 76%. The HOE-694-resistant NHE activities in the cultured epithelia of efferent duct and cauda epididymidis were completely inhibited by 20 microM S3226 (3-[2-(3-guanidino-2-methyl-3-oxo-propenyl)-5-methyl-phenyl]-N:-isopropylidene-2-methyl-acrylamide dihydrochloride), a NHE3 inhibitor, and 300 microM HOE-694 (a dose that can completely block NHE2), respectively. These results indicated that NHE1, NHE2, and NHE3 were expressed in the cultured epithelial cells of the efferent duct, whereas only NHE1 and NHE2 were expressed in the cultured epithelial cells of the cauda epididymidis. It is suggested that NHE1 may provide "housekeeping" functions in both epithelia, whereas NHE2 in the cauda epididymidis and NHE3 in the efferent duct may be involved in Na+ reabsorption and regulation of pH of the luminal fluid.

摘要

尽管早期研究表明大鼠附睾中存在钠氢交换体(NHEs),但对于各种NHE亚型的区域分布及其功能却知之甚少。在本研究中,我们对输出小管和附睾尾的培养上皮细胞中不同NHE亚型的表达进行了研究。逆转录-聚合酶链反应显示,在两种培养上皮细胞中均存在NHE1、NHE2和NHE3的信使核糖核酸,但未检测到NHE4的信使核糖核酸。蛋白质印迹分析检测到两种培养上皮细胞中均存在NHE1和NHE2蛋白,但仅在输出小管的培养上皮细胞中检测到NHE3蛋白。免疫组织化学研究表明,NHE2定位于纤毛细胞的细胞质中,而NHE3定位于输出小管主细胞的顶端膜。两种培养上皮细胞中的NHE活性均被NHE1抑制剂10微摩尔HOE-694(3-甲基磺酰基-4-哌啶基苯甲酰胍甲磺酸盐)抑制了约76%。输出小管和附睾尾培养上皮细胞中对HOE-694耐药的NHE活性分别被NHE3抑制剂20微摩尔S3226(3-[2-(3-胍基-2-甲基-3-氧代丙烯基)-5-甲基苯基]-N-异丙叉基-2-甲基丙烯酰胺二盐酸盐)和300微摩尔HOE-694(可完全阻断NHE2的剂量)完全抑制。这些结果表明,NHE1、NHE2和NHE3在输出小管的培养上皮细胞中表达,而在附睾尾的培养上皮细胞中仅表达NHE1和NHE2。提示NHE1可能在两种上皮细胞中发挥“管家”功能,而附睾尾中的NHE2和输出小管中的NHE3可能参与钠离子重吸收和管腔液pH值的调节。

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