Garcia-Romeu F, Borgese F, Guizouarn H, Fiévet B, Motais R
Laboratoire J. Maetz, Département de Biologie Cellulaire et Moléculaire, C.E.A., Villefranche sur Mer, France.
Cell Mol Biol (Noisy-le-grand). 1996 Nov;42(7):985-94.
In response to swelling cells recover their volume by releasing ions (mainly K+, Cl-) and different organic solutes (e.g. taurine) via volume-sensitive pathways. Depending on the cause of swelling (net uptake of electrolytes or decrease in external osmolality) cells use specifically some of these pathways. Previous data indicate that the anion exchanger (AE1) is involved in the choice of the regulatory pattern the cells adopt. Molecular cloning and functional expression of AE1 from the trout erythrocyte shows that this anion exchanger can function as a channel mediating taurine fluxes. In the erythrocyte, the channel activation depends on the conditions as the cell is swollen: when swelling is caused by an accumulation of electrolytes (resulting in an increase of the intracellular ionic strength) the channel is not activated and the regulatory volume decrease occurs exclusively by a release of K and Cl via a KCl cotransporter. When swelling is caused by hypotonic shock (resulting in a decrease in intracellular ionic strength) the KCl cotransporter is then mainly inactivated or even silent; conversely the channel is activated and allows volume recovery by mediating the release of both taurine and probably K and Cl. The possibility that AEs function as volume-activated taurine channels in other cell types and as a malaria-induced channel in malaria-infected human red cells is considered.
作为对肿胀的反应,细胞通过容积敏感途径释放离子(主要是K⁺、Cl⁻)和不同的有机溶质(如牛磺酸)来恢复其体积。根据肿胀的原因(电解质的净摄取或细胞外渗透压的降低),细胞会特异性地使用其中一些途径。先前的数据表明,阴离子交换蛋白(AE1)参与了细胞所采用的调节模式的选择。从虹鳟红细胞中克隆AE1并进行功能表达,结果表明这种阴离子交换蛋白可以作为介导牛磺酸通量的通道发挥作用。在红细胞中,通道的激活取决于细胞肿胀的条件:当肿胀是由电解质积累引起时(导致细胞内离子强度增加),通道不会被激活,调节性容积减小仅通过KCl共转运体释放K⁺和Cl⁻来实现。当肿胀是由低渗休克引起时(导致细胞内离子强度降低),KCl共转运体则主要失活甚至不起作用;相反,通道被激活,并通过介导牛磺酸以及可能的K⁺和Cl⁻的释放来实现容积恢复。人们还考虑了AE在其他细胞类型中作为容积激活的牛磺酸通道以及在疟疾感染的人类红细胞中作为疟疾诱导通道发挥作用的可能性。