Heterogeneity of I^sub K1^ in the mouse heart

Previous studies have shown that cardiac inward rectifier potassium current (I^sub K1^) channels are heteromers of distinct Kir2 subunits and suggested that species- and tissue-dependent expression of these subunits may underlie variability of I^sub K1^. In this study, we investigated the contributi...

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Bibliographic Details
Published in:American journal of physiology. Heart and circulatory physiology 2007-12, Vol.293 (6), p.H3558
Main Authors: Panama, Brian K, McLerie, Meredith, Lopatin, Anatoli N
Format: Article
Language:English
Subjects:
Cells
Heart failure
Kinetics
Potassium
Rodents
Studies
Online Access:Get full text
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Summary:Previous studies have shown that cardiac inward rectifier potassium current (I^sub K1^) channels are heteromers of distinct Kir2 subunits and suggested that species- and tissue-dependent expression of these subunits may underlie variability of I^sub K1^. In this study, we investigated the contribution of the slowly activating Kir2.3 subunit and free intracellular polyamines (PAs) to variability of I^sub K1^ in the mouse heart. The kinetics of activation was measured in Kir2 concatemeric tetramers with known subunit stoichiometry. Inclusion of only one Kir2.3 subunit to a Kir2.1 channel led to an approximate threefold slowing of activation kinetics, with greater slowing on subsequent additions of Kir2.3 subunits. Activation kinetics of I^sub K1^ in both ventricles and both atria was found to correspond to fast-activating Kir2.1/Kir2.2 channels, suggesting no major contribution of Kir2.3 subunits. In contrast, I^sub K1^ displayed significant variation in both the current density and inward rectification, suggesting involvement of intracellular PAs. The total levels of PAs were similar across the mouse heart. Measurements of the free intracellular PAs in isolated myocytes, using transgenically expressed Kir2.1 channels as PA sensors, revealed "microheterogeneity" of I^sub K1^ rectification as well as lower levels of free PAs in atrial myocytes compared with ventricular cells. These findings provide a quantitative explanation for the regional heterogeneity of I^sub K1^. [PUBLICATION ABSTRACT]
ISSN:0363-6135
1522-1539