Jacobsen Jack H, Clement Christian A, Friis Martin B, Lambert Ian H
Department of Biology, The August Krogh Building, Universitetsparken 13, 2100, Copenhagen Ø, Denmark.
Pflugers Arch. 2008 Nov;457(2):327-37. doi: 10.1007/s00424-008-0517-2. Epub 2008 Apr 30.
Inhibition of the constitutively active casein kinase 2 (CK2) with 2-dimethyl-amino-4,5,6,7-tetrabromo-1H-benzimidasole stimulates the Na(+)-dependent taurine influx via the taurine transporter TauT in NIH3T3 cells. CK2 inhibition reduces the TauT mRNA level and increases the localization of TauT to ER but has no detectable effect on TauT protein expression. On the other hand, CK2 inhibition increases the affinity of TauT towards Na(+ )and reduces the Na(+)/taurine stoichiometry for active taurine uptake. It is suggested that CK2 controls the cellular taurine uptake in unperturbated NIH3T3 cells, i.e., inhibition of CK2 increases the affinity of TauT towards Na(+) and hence Na(+)-dependent taurine uptake.
用2-二甲基氨基-4,5,6,7-四溴-1H-苯并咪唑抑制组成型活性酪蛋白激酶2(CK2),可通过牛磺酸转运体TauT刺激NIH3T3细胞中Na(+)依赖性牛磺酸内流。CK2抑制降低了TauT mRNA水平,并增加了TauT在内质网的定位,但对TauT蛋白表达没有可检测的影响。另一方面,CK2抑制增加了TauT对Na(+)的亲和力,并降低了主动摄取牛磺酸时的Na(+)/牛磺酸化学计量比。提示CK2在未受干扰的NIH3T3细胞中控制细胞对牛磺酸的摄取,即抑制CK2可增加TauT对Na(+)的亲和力,从而增加Na(+)依赖性牛磺酸摄取。