Literature DB >> 19460073

Synergistic effects of inward rectifier (I) and pacemaker (I) currents on the induction of bioengineered cardiac automaticity.

Yau-Chi Chan1, Chung-Wah Siu, Yee-Man Lau, Chu-Pak Lau, Ronald A Li, Hung-Fat Tse.   

Abstract

INTRODUCTION: Normal heart rhythms originate in the sinoatrial node. HCN-encoded funny current (I(f)) and the Kir2-encoded inward rectifier (I(K1)) counteract each other by respectively oscillating and stabilizing the negative resting membrane potential, and controlling action potential firing. Therefore, I(K1) suppression and I(f) overexpression have been independently exploited to convert cardiomyocytes (CMs) into AP-firing bioartificial pacemakers. Although the 2 strategies have been largely assumed synergistic, their complementarity has not been investigated. METHODS AND
RESULTS: We explored the interrelationships of automaticity, I(f) and I(K1) by transducing single left ventricular (LV) CMs isolated from guinea pig hearts with the recombinant adenoviruses Ad-CMV-GFP-IRES-HCN1-AAA and/or Ad-CGI-Kir2.1 to mediate their current densities via a whole-cell patch clamp technique at 37 degrees C. Results showed that Ad-CGI-HCN1-AAA but not Ad-CGI-Kir2.1 transduction induced automaticity (181.1 +/- 13.1 bpm). Interestingly, Ad-CGI-HCN1-AAA/Ad-CGI-Kir2.1 cotransduction significantly promoted the induced firing frequency (320.0 +/- 15.8 bpm; P < 0.05). Correlation analysis revealed that the firing frequency, phase-4 slope and APD(90) of AP-firing LV CMs were correlated with I(f) (R(2) > 0.7) only when -2 >I(K1) >-4 pA/pF but not with I(K1) over the entire I(f) ranges examined (0.02 < R(2) < 0.4). Unlike I(f), I(K1) displayed correlation with neither the phase-4 slope (R(2)= 0.02) nor phase-4 length (R(2)= 0.04) when -2 > I(f) > -4 pA/pF. As anticipated, however, APD(90) was correlated with I(K1) (R(2)= 0.4).
CONCLUSION: We conclude that an optimal level of I(K1) maintains a voltage range for I(f) to operate most effectively during a dynamic cardiac cycle.

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Year:  2009        PMID: 19460073      PMCID: PMC2739246          DOI: 10.1111/j.1540-8167.2009.01475.x

Source DB:  PubMed          Journal:  J Cardiovasc Electrophysiol        ISSN: 1045-3873


  31 in total

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Authors:  J Qu; A Barbuti; L Protas; B Santoro; I S Cohen; R B Robinson
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Journal:  Mol Pharmacol       Date:  2002-01       Impact factor: 4.436

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Review 4.  The sinoatrial node, a heterogeneous pacemaker structure.

Authors:  M R Boyett; H Honjo; I Kodama
Journal:  Cardiovasc Res       Date:  2000-09       Impact factor: 10.787

5.  Mechanistic role of I(f) revealed by induction of ventricular automaticity by somatic gene transfer of gating-engineered pacemaker (HCN) channels.

Authors:  Tian Xue; Chung-Wah Siu; Deborah K Lieu; Chu-Pak Lau; Hung-Fat Tse; Ronald A Li
Journal:  Circulation       Date:  2007-03-26       Impact factor: 29.690

Review 6.  New insights into pacemaker activity: promoting understanding of sick sinus syndrome.

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7.  Overexpression of HCN-encoded pacemaker current silences bioartificial pacemakers.

Authors:  Deborah K Lieu; Yau Chi Chan; Chu Pak Lau; Hung Fat Tse; Chung Wah Siu; Ronald A Li
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8.  Dual gene therapy with SERCA1 and Kir2.1 abbreviates excitation without suppressing contractility.

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9.  Structural and functional determinants in the S5-P region of HCN-encoded pacemaker channels revealed by cysteine-scanning substitutions.

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10.  Dominant-negative suppression of HCN1- and HCN2-encoded pacemaker currents by an engineered HCN1 construct: insights into structure-function relationships and multimerization.

Authors:  Tian Xue; Eduardo Marbán; Ronald A Li
Journal:  Circ Res       Date:  2002-06-28       Impact factor: 17.367

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  16 in total

1.  Automaticity and conduction properties of bio-artificial pacemakers assessed in an in vitro monolayer model of neonatal rat ventricular myocytes.

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2.  Electrical stimulation promotes maturation of cardiomyocytes derived from human embryonic stem cells.

Authors:  Yau-Chi Chan; Sherwin Ting; Yee-Ki Lee; Kwong-Man Ng; Jiao Zhang; Zi Chen; Chung-Wah Siu; Steve K W Oh; Hung-Fat Tse
Journal:  J Cardiovasc Transl Res       Date:  2013-10-01       Impact factor: 4.132

3.  Kir2 inward rectification-controlled precise and dynamic balances between Kir2 and HCN currents initiate pacemaking activity.

Authors:  Kuihao Chen; Dongchuan Zuo; Sho-Ya Wang; Haijun Chen
Journal:  FASEB J       Date:  2018-01-12       Impact factor: 5.191

4.  Epigenetic regulation of the electrophysiological phenotype of human embryonic stem cell-derived ventricular cardiomyocytes: insights for driven maturation and hypertrophic growth.

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5.  A Singular Role of IK1 Promoting the Development of Cardiac Automaticity during Cardiomyocyte Differentiation by IK1 -Induced Activation of Pacemaker Current.

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Review 7.  Nonlinear dynamics in cardiology.

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Review 8.  Gene- and cell-based bio-artificial pacemaker: what basic and translational lessons have we learned?

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Journal:  Gene Ther       Date:  2012-06       Impact factor: 5.250

9.  Probing the bradycardic drug binding receptor of HCN-encoded pacemaker channels.

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Review 10.  Stem cell-based biological pacemakers from proof of principle to therapy: a review.

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