Hara Y, Nikamoto A, Kojima T, Matsumoto A, Nakao M
Department of Biochemistry, Tokyo Medical and Dental University School of Medicine, Japan.
FEBS Lett. 1988 Sep 26;238(1):27-30. doi: 10.1016/0014-5793(88)80218-7.
The cDNAs encoding alpha 3-subunits of rat brain Na+,K+-ATPase and the neomycin resistance gene were incorporated into BALB/c 3T3 cells by the co-transfection method. Stably transformed cells were selected with 300 micrograms/ml of neomycin (G-418) for 6 weeks. Northern blot analysis using the 3'-non-translated region of the cDNA as a probe revealed that the alpha 3 mRNA appeared in transfected cells. Na+,K+-ATPase activity of the transfected cells was twice that of wild-type cells. Regarding ouabain sensitivity, the Na+,K+-ATPase showed two Ki values for ouabain (8 x 10(-8) and 4.5 x 10(-5) M) in transfected cells while wild-type cells displayed only the higher value. Ouabain sensitivity of Rb+ uptake also demonstrated two Ki values in the transfected cells (8 x 10(-8) and 4 x 10(-5) M) and a Ki in wild-type cells of 4 x 10(-5) M. It is concluded that alpha 3 is a highly ouabain-sensitive catalytic subunit of Na+,K+-ATPase. It is also suggested that ouabain sensitivity is exclusively determined by the properties of the alpha-subunit rather than the beta-subunit. This is the first report on the catalytic characteristics of the alpha 3 isoform of Na+,K+-ATPase.
通过共转染法将编码大鼠脑Na +,K + -ATP酶α3亚基的cDNA和新霉素抗性基因导入BALB / c 3T3细胞。用300微克/毫升新霉素(G-418)筛选稳定转化的细胞6周。以cDNA的3'非翻译区为探针进行Northern印迹分析,结果显示α3 mRNA出现在转染细胞中。转染细胞的Na +,K + -ATP酶活性是野生型细胞的两倍。关于哇巴因敏感性,转染细胞中的Na +,K + -ATP酶对哇巴因显示出两个Ki值(8×10(-8)和4.5×10(-5)M),而野生型细胞仅显示较高的值。转染细胞中Rb +摄取的哇巴因敏感性也显示出两个Ki值(8×10(-8)和4×10(-5)M),野生型细胞中的Ki为4×10(-5)M。结论是α3是Na +,K + -ATP酶的高度哇巴因敏感催化亚基。还表明哇巴因敏感性完全由α亚基而非β亚基的性质决定。这是关于Na +,K + -ATP酶α3同工型催化特性的首次报道。