Shugrue C A, Obermüller N, Bachmann S, Slayman C W, Reilly R F
Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
J Am Soc Nephrol. 1999 Aug;10(8):1649-57. doi: 10.1681/ASN.V1081649.
LLC-PK1 cells, an established line from pig kidney, express basolateral and apical Na+/H+ exchangers that can be distinguished by their differing sensitivities to the amiloride analog N-ethyl-N-isopropylamiloride (EIPA). It has been shown previously that the basolateral exchanger is encoded by NHE1. In the present study, a combination of reverse transcription-PCR, 5' RACE, and genomic library screening was used to clone the coding region of the porcine NHE3 gene. There was significant homology between the LLC-PK1 sequence and the previously reported rabbit and rat NHE3 genes, with nucleotide and deduced amino acid identities of 87 and 85% in rabbit, and 85 and 87% in rat, respectively. To study expression patterns, Northern analysis was carried out using an NHE3 cDNA to probe poly(A)+ RNA isolated from LLC-PK1 cells, and from pig kidney cortex. In all three cases, a major transcript of 6.1 kb was detected along with two minor transcripts of 4.7 and 3.8 kb. In situ hybridization with two different NHE3 probes gave intense labeling of the distal convoluted tubule in pig kidney but (unexpectedly) no detectable labeling of the proximal tubule. These studies suggest that there are marked species differences in NHE3 expression in the distal nephron.
LLC-PK1细胞系源自猪肾,表达基底外侧和顶端的Na+/H+交换体,它们可通过对氨氯吡脒类似物N-乙基-N-异丙基氨氯吡脒(EIPA)的不同敏感性来区分。先前已表明基底外侧交换体由NHE1编码。在本研究中,采用逆转录聚合酶链反应(RT-PCR)、5'端快速扩增cDNA末端(5' RACE)和基因组文库筛选相结合的方法克隆猪NHE3基因的编码区。LLC-PK1序列与先前报道的兔和大鼠NHE3基因之间存在显著同源性,与兔的核苷酸和推导氨基酸同一性分别为87%和85%,与大鼠的分别为85%和87%。为研究表达模式,使用NHE3 cDNA对从LLC-PK1细胞和猪肾皮质分离的多聚腺苷酸加尾RNA(poly(A)+ RNA)进行Northern印迹分析。在所有三种情况下,均检测到一条6.1 kb的主要转录本以及两条4.7 kb和3.8 kb的次要转录本。用两种不同的NHE3探针进行原位杂交,结果显示猪肾远曲小管有强烈标记,但(出乎意料地)近端小管未检测到标记。这些研究表明,远端肾单位中NHE3的表达存在明显的物种差异。