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.
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1 August 1989
Article|
August 01 1989
Glutaraldehyde fixation of the cAMP-dependent Na+/H+ exchanger in trout red cells.
R Motais,
R Motais
Laboratoire Jean Maetz, Département de Biologie du Commissariat à l'Energie Atomique, Villefranche-sur-Mer, France.
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F Borgese,
F Borgese
Laboratoire Jean Maetz, Département de Biologie du Commissariat à l'Energie Atomique, Villefranche-sur-Mer, France.
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U Scheuring,
U Scheuring
Laboratoire Jean Maetz, Département de Biologie du Commissariat à l'Energie Atomique, Villefranche-sur-Mer, France.
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F Garcia-Romeu
F Garcia-Romeu
Laboratoire Jean Maetz, Département de Biologie du Commissariat à l'Energie Atomique, Villefranche-sur-Mer, France.
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R Motais
,
F Borgese
,
U Scheuring
,
F Garcia-Romeu
Laboratoire Jean Maetz, Département de Biologie du Commissariat à l'Energie Atomique, Villefranche-sur-Mer, France.
Online ISSN: 1540-7748
Print ISSN: 0022-1295
J Gen Physiol (1989) 94 (2): 385–400.
Citation
R Motais, F Borgese, U Scheuring, F Garcia-Romeu; Glutaraldehyde fixation of the cAMP-dependent Na+/H+ exchanger in trout red cells.. J Gen Physiol 1 August 1989; 94 (2): 385–400. doi: https://doi.org/10.1085/jgp.94.2.385
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