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戊二醛对虹鳟红细胞中cAMP依赖性钠/氢交换体的固定作用。

Glutaraldehyde fixation of the cAMP-dependent Na+/H+ exchanger in trout red cells.

作者信息

Motais R, Borgese F, Scheuring U, Garcia-Romeu F

机构信息

Laboratoire Jean Maetz, Département de Biologie du Commissariat à l'Energie Atomique, Villefranche-sur-Mer, France.

出版信息

J Gen Physiol. 1989 Aug;94(2):385-400. doi: 10.1085/jgp.94.2.385.

Abstract

It has been shown that the addition of a beta-adrenergic catecholamine to a trout red blood cell suspension induces a 60-100-fold increase of sodium permeability resulting from the activation of a cAMP-dependent Na+/H+ antiport. Subsequent addition of propranolol almost instantaneously reduces the intracellular cAMP concentration, and thus the Na permeability, to their basal values (Mahé et al., 1985). If glutaraldehyde (0.06-0.1%) is added when the Na+/H+ exchanger is activated after hormonal stimulation, addition of propranolol no longer inhibits Na permeability: once activated and fixed by glutaraldehyde, the cAMP dependence disappears. Glutaraldehyde alone causes a rapid decrease in the cellular cAMP concentration. In its fixed state the antiporter is fully amiloride sensitive. The switching on of the Na+/H+ exchange by cAMP is rapidly (2 min) followed by acute but progressive desensitization of the exchanger (Garcia-Romeu et al., 1988). The desensitization depends on the concentration of external sodium, being maximal at a normal Na concentration (145 mM) and nonexistent at a low Na concentration (20 mM). If glutaraldehyde is added after activation in nondesensitizing conditions (20 mM Na), transfer to a Na-rich medium induces only a very slight desensitization: thus the fixative can "freeze" the exchanger in the nondesensitizing conformation. NO3- inhibits the activity of the cAMP-dependent Na+/H+ antiporter of the trout red blood cell (Borgese et al., 1986). If glutaraldehyde is added when the cells are activated by cAMP in a chloride-containing medium, the activity of the exchanger is no longer inhibited when Cl- is replaced by NO3-. Conversely, after fixation in NO3- medium replacement of NO3- by Cl- has very little stimulatory effect. This indicates that the anion dependence is not a specific requirement for the exchange process but that the anion environment is critical for the switching on of the Na+/H+ exchanger and for the maintenance of its activated configuration.

摘要

研究表明,向虹鳟红细胞悬液中添加β - 肾上腺素能儿茶酚胺会导致钠通透性增加60 - 100倍,这是由cAMP依赖性Na⁺/H⁺逆向转运体的激活所致。随后添加普萘洛尔几乎能瞬间将细胞内cAMP浓度以及钠通透性降低至基础值(马赫等人,1985年)。如果在激素刺激后Na⁺/H⁺交换体被激活时添加戊二醛(0.06 - 0.1%),那么添加普萘洛尔就不再抑制钠通透性:一旦被戊二醛激活并固定,对cAMP的依赖性就消失了。单独的戊二醛会导致细胞内cAMP浓度迅速降低。在其固定状态下,逆向转运体对氨氯吡咪完全敏感。cAMP开启Na⁺/H⁺交换后很快(2分钟),交换体就会出现急性但渐进性的脱敏现象(加西亚 - 罗梅乌等人,1988年)。脱敏取决于细胞外钠的浓度,在正常钠浓度(145 mM)时最大,在低钠浓度(20 mM)时不存在。如果在非脱敏条件(20 mM Na)下激活后添加戊二醛,转移到富含钠的培养基中只会引起非常轻微的脱敏:因此固定剂可以将交换体“冻结 ”在非脱敏构象中。NO₃⁻会抑制虹鳟红细胞中cAMP依赖性Na⁺/H⁺逆向转运体的活性(博尔盖塞等人,1986年)。如果在含氯培养基中细胞被cAMP激活时添加戊二醛,当Cl⁻被NO₃⁻取代时,交换体的活性不再受到抑制。相反,在NO₃⁻培养基中固定后,用Cl⁻取代NO₃⁻几乎没有刺激作用。这表明阴离子依赖性并非交换过程的特定要求,而是阴离子环境对于Na⁺/H⁺交换体的开启及其激活构型的维持至关重要。

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