Hamabata Takashi, Liu Cailian, Takeda Yoshifumi
Research Institute, International Medical Center of Japan, Tokyo 162-8655, Japan.
Microb Pathog. 2002 Jun;32(6):273-7. doi: 10.1006/mpat.2002.0502.
Analysis of osmotic water permeability of aquaporin (AQP) 1, AQP3 and AQP4, which are expressed in human small intestine, in the presence or absence of cholera toxin (CT) was performed using a Xenopus oocyte expression system. When treated with CT, water permeability of AQP4 was facilitated while that of AQP3 was suppressed. AQP1 did not show any significant change of water permeability when treated with CT. An adenylyl cyclase accelerator forskolin showed similar effects as CT did, suggesting that changes of the water permeability of AQP4 and AQP3 were due to an increase of intracellular cAMP concentration. A possibility that these AQPs are responsible molecules for causing acute secretory diarrhoea as in cholera is considered.
利用非洲爪蟾卵母细胞表达系统,对在人小肠中表达的水通道蛋白(AQP)1、AQP3和AQP4在存在或不存在霍乱毒素(CT)的情况下的渗透水通透性进行了分析。用CT处理时,AQP4的水通透性增强,而AQP3的水通透性受到抑制。用CT处理时,AQP1的水通透性未显示出任何显著变化。腺苷酸环化酶激活剂福斯可林显示出与CT类似的作用,这表明AQP4和AQP3水通透性的变化是由于细胞内cAMP浓度的增加所致。人们认为这些水通道蛋白可能是导致如霍乱那样的急性分泌性腹泻的责任分子。