Zeng X T, Hara M, Inagaki C
Department of Pharmacology, Kansai Medical University, Osaka, Japan.
Brain Res. 1994 Mar 28;641(1):167-70. doi: 10.1016/0006-8993(94)91833-3.
Rat brain Cl(-)-ATPase was solubilized and reconstituted in asolectin liposomes. Phosphatidylinositol-4-monophosphate increased Cl(-)-ATPase and ATP-dependent Cl- uptake activities in proteoliposomes. The ATP-dependent Cl- uptake was inhibited by a Cl(-)-ATPase inhibitor, ethacrynic acid, and increased at an inside-positive membrane potential or in the presence of a protonophore. These findings suggest that Cl(-)-ATPase is an electrogenic Cl- transporter, or a primary Cl- pump, probably regulated by phosphoinositide turnover in vivo.
大鼠脑Cl(-)-ATP酶被溶解并重新组装到大豆卵磷脂脂质体中。磷脂酰肌醇-4-单磷酸增加了蛋白脂质体中Cl(-)-ATP酶和ATP依赖的Cl-摄取活性。ATP依赖的Cl-摄取受到Cl(-)-ATP酶抑制剂依他尼酸的抑制,并在膜电位为内正或存在质子载体的情况下增加。这些发现表明,Cl(-)-ATP酶是一种生电Cl-转运体,或一种初级Cl-泵,可能在体内受磷酸肌醇代谢的调节。