Developmental evolution of the delayed rectifier current IKs in canine heart appears dependent on the beta subunit minK

• Published in: Heart rhythm Vol. 1; no. 6; p. 704
• Main Authors: Krishnamurthy, Ganga, Patberg, Kornelis W, Obreztchikova, Maria N, Rybin, Andrew V, Rosen, Michael R
• Format: Journal Article
• Language: English
• Published: United States 01-12-2004
• Subjects: Aging - metabolism; Animals; Blotting, Western; Cation Transport Proteins - metabolism; Dogs; Ether-A-Go-Go Potassium Channels; Female; Heart Ventricles - cytology; Male; Myocytes, Cardiac - metabolism; Pericardium - cytology; Polymerase Chain Reaction; Potassium Channels, Voltage-Gated - metabolism; RNA, Messenger - metabolism
• ISSN: 1547-5271
• DOI: 10.1016/j.hrthm.2004.08.012

We tested the hypothesis that the developmental changes occurring in I(Kr) and I(Ks) can be explained by changes in the expression of ERG encoding I(Kr), and KCNQ1, the beta subunit minK, and the recently reported subunit FHL2 encoding I(Ks).
The delayed rectifier current contributes importantly to the developmental evolution of the canine myocardial action potential. Specifically, in left ventricular epicardial myocytes, I(Ks) is absent and I(Kr) is the major repolarizing current until age 4 weeks. With subsequent development, I(Ks) density increases and I(Kr) decreases, resulting in an altered voltage-time course of repolarization.
We used Western blotting and real-time polymerase chain reaction to compare the expression of ERG, KCNQ1, minK, and FHL2 in 1-week-old pups and adult dogs.
ERG levels are high at 1 week and decrease significantly with age, consistent with developmental decrease in I(Kr). Whereas expression of KCNQ1 and FHL2 is unchanged between the two age groups, minK is minimally expressed at 1 week and increases in adults, consistent with developmental increase in I(Ks).
A reduction in ERG explains the developmental decrease in I(Kr), whereas the accessory subunit minK appears to be the critical determinant of developmental evolution of I(Ks).