Indian Pacing Electrophysiol. J.

ISSN 0972-6292

Home Page Current Issue List of Editors

Indian Pacing Electrophysiol. J. 2006;6(1):1-5                 Editorial

Biological Pacemakers

Download PDF 132 KB 

Rajesh G, MBBS, MD, DNB, DM; Johnson Francis, MBBS, MD, DM, FCSI

Department of Cardiology, Medical College Hospital, Calicut, Kerala, India.

Address for correspondence: Dr. Rajesh G, MBBS, MD, DNB, DM, Assistant Professor, Department of Cardiology, Medical College Hospital, Calicut, Kerala, India. E- mail:


            Genetically engineered pacemakers could be a possible alternative to implantable electronic devices for the treatment of bradyarrhythmias. The strategies include upregulation of beta adrenergic receptors, conversion of myocytes into pacemaker cells and stem cell therapy. Pacemaker activity in adult ventricular myocytes is normally repressed by the inward rectifier potassium current (IK1). The IK1 current is encoded by the Kir2 gene family. Use of a negative construct that suppresses current when expressed with wild-type Kir2.1 is an experimental approach for genesis of genetic pacemaker. Hyperpolarisation activated cyclic nucleotide gated (HCN) channels which generate If current, the pacemaker current of heart can be delivered to heart by using stem cell therapy approach and viral vectors. The unresolved issues include longevity and stability of pacemaker genes, limitations involved in adenoviral and stem cell therapy and creation of genetic pacemakers which can compete with the electronic units.
Keywords: Gene therapy, Pacemaker current, HCN channels.

            Implantable electronic pacemakers remain the treatment of choice for high degree atrioventricular blocks and sinus node dysfunction. The shortcomings of electronic pacemakers include limited battery life, need for lead implantation into heart and lack of response to autonomic and physiologic demands on the heart.  Molecular approaches to the development of a biological pacemaker are a conceptually attractive alternate treatment modality for heart blocks. The approaches attempted to provide such pacemaker function  include up regulation of β2 adrenergic receptors1, down regulation of K+ current IK12 and over expression of HCN2 (hyperpolarisation activated cyclic nucleotide gated) channels the molecular correlate of the endogenous cardiac pacemaker current If 3. The genetic treatment can be applied to heart by plasmid injection, use of viral constructs or stem cell therapy4,5.

Molecular targets for genesis of biological pacemaker

β2 adrenergic receptors

            The sinus node has a higher density of β adrenergic receptors (βAR) compared with surrounding atrium1. This density of βAR and its regulation of If current suggest that increases in the density of βAR in the vicinity of the sinus node may lead to an increase in heart rate. The up regulation of β2 adrenergic receptors can be achieved by plasmid injection into heart. It was noted that after injection of plasmids in porcine right atrium heart rates were 50% faster than those of controls. One potential limitation of this strategy is that the diseased endogenous cardiac pacemaker mechanisms are left intact and the β2 receptor is used as a nonspecific stimulator of heart rate. It can influence other catecholamine sensitive channels also.

HCN channel and If current
                  Action potential of pacing cells is unique in that they have a slow depolarizing phase, rendering them spontaneously active6. The depolarization involves interaction between HCN channels and L & T type calcium channels. The modification of these channels is a therapeutic target.
            HCN channels generate If current which contribute to genesis of pacemaker activity. If channel is activated on membrane hyperpolarisation rather than on depolarization7. It has four fold selectivity for K+ than Na+. The typical features of If current include activation by hyperpolarized membrane potential, conduction of Na+ and K+, modulation by cyclic adenosine monophospate (CAMP) and blockade by cesium (Cs+)8. HCN generated current also has the above features. Four different HCN genes have been identified9. HCN1 is the most rapidly acting channel, HCN4 the slowest with HCN2 and 3 possessing intermediate kinetics10. HCN1, 2 and 4 have been found to express in adult heart, HCN4 being the most highly expressed one in SA node. HCN2 expression was noted in atrium, ventricle and SA node.
            HCN can be delivered to heart by adenoviral construct or using stem cells. The nucleic acids delivered by adenoviruses do not integrate into genome as they are episomal. Stem cell therapy may be more promising than viral strategy. The approach using HCN may be less problematic and proarrythmic as it incorporates the endogenous pacemaker channel gene, which selectively activates only during diastole14.

Inward Rectifier Potassium Current (IK1)
            IK1 and other background K+ selective currents contribute to action potential depolarization and establish diastolic resting membrane potential. Down regulation of the background K+ current IK1 is one of the approaches attempted to provide pacemaker function. Genetic suppression of IK1 can converts quiescent myocytes into pacemaker cells.   
            IK1 is the classical inward rectifier potassium current. Inwardly rectifying K+ channels (Kir) are responsible for stabilizing the resting membrane potential. Inward rectification is a phenomenon in which conductance of a Kir channel increases with hyperpolarisation but decreases with depolarization. Rectification in Kir channels results from voltage dependent channel block by intracellular cations12. IK1 is absent or poorly expressed in sinus and AV nodal cells. Native IK1 in human ventricular myocytes is reduced by adrenergic receptor stimulation.
            It was observed that a dominant negative strategy to reduce IK1, which usually maintain ventricular myocytes at negative membrane potentials, induced spontaneous impulse initiation in guinea pig heart. The inward rectifier potassium current is encoded by Kir2 gene family. Replacement of 3 amino acid residues in the pore structure of Kir2.1 creates a dominant negative construct12. Downregulation of IK1 removes an important determinant of repolarisation leading to prolonged repolarisation in cells lacking this current13. This may result in excessive dispersion of repolarisation leading to theoretical risk of proarrhythmia.

Stem cell therapy

            Human embryonic stem cells can be used to create pacemakers or adult mesenchymal stem cells may be used as platforms for delivery of pacemaker genes to myocardium. The advantage of these cells includes their ability to make functional gap junctions and generate spontaneous rhythms15. The approach using embryonic stem cells carry the problems of identifying appropriate cell lineages, possibility of stem cell differentiation into lines other than pacemaker cells, and potential for neoplasia. Adult mesenchymal stem cells are biologically inert vectors which can deliver genetic information to myocardium. Human mesenchymal stem cells (hMSCs) as a platform for delivery of genes into heart is a more attractive option because they can be obtained in large numbers, easily expanded in culture, capable of long term transgene expression and their administration can be autologous or via banked stores15.

Gene therapy versus stem cell therapy

            In gene therapy a cardiac myocyte is converted into a pacemaker cell whereas in stem cell therapy myocytes retain their original function. An inherent problem of gene therapy is use of viruses. Replication deficient adenoviruses with little infectious potential lead to only transient improvement in pacemaker function. Retroviruses may be carcinogenic and infective.

Important studies on biological pacemakers

1. Molecular transfer of the human β2 Adrenergic receptor cDNA
            Effects of transferring the human β2 adrenergic receptor were studied by Edelberg JM et al1 in chronotropy studies with isolated myocytes, and transplanted as well as endogenous murine heart. Murine embryonic cardiac myocytes were transiently transfected with plasmid constructs. The total percentage of spontaneously contracting myocytes was greater in β2AR transfected cells compared with controls. Also the percentage of myocytes with chronotropic rates more than 60 beats per minute was greater in β2AR population than controls. To study the ex vivo effects of targeted expression of β2AR a murine neonatal cardiac transplantation model was used. Injection of β2AR construct increased the heart rate by 40%. These studies demonstrate that local targeting of gene expression may be a feasible modality to regulate the cardiac pacemaking activity.

2. Local expression of HCN2 in canine left atrium
            Research by Jihong Qu et al13 showed that HCN2 over expression provides an If - based pacemaker current sufficient to drive the heart when injected into a localized region of atrium. Adenoviral constructs of mouse HCN2 and green fluorescent protein (GFP) or GFP alone were injected into LA, terminal studies performed 3-4 days later, myocytes examined for native and expressed pacemaker current (If). Spontaneous LA rhythms occurred after vagal stimulation-induced sinus arrest in 4 of 4 HCN2 + GFP dogs and 0 of 3 GFP dogs (P<0.05).

3. Biological pacemaker implanted in canine left bundle branch
            Alexi N. Plotnikov et al14 studied the effect of administration of the HCN2 gene to the left bundle branch system of dogs. An adenoviral construct incorporating HCN2 and green fluorescent protein (GFP) as a marker was injected via catheter under fluoroscopic control into the posterior division of the LBB. Controls were injected with an adenoviral construct of GFP alone or saline. During vagal stimulation, HCN2 injected dogs showed rhythms originating from the left ventricle, the rate of which was significantly more rapid than controls.

4. Human mesenchymal Stem Cells as a gene delivery system to create cardiac pacemaker
            Potapova I et al3 tested the ability of human mesenchymal stem cells to deliver a biological pacemaker to the heart. hMSCs transfected with a cardiac pacemaker gene, mHCN2, by electroporation expressed current as If - like. They demonstrated that genetically modified hMSCs can express functional HCN2 channels in vitro and in vivo, mimicking over exression of HCN2 genes in cardiac myocytes, and represent a noval delivery system for pacemaker genes into the heart or other electrical syncytia.

Limitations of approaches to development of biological pacemaker

            Use of viruses to deliver the necessary genes has inherent problems. Replication deficient adenoviruses that have little infectious potential lead to only   transient improvement in pacemaker function as well as potential inflammatory responses. Retroviruses carry a risk of carcinogenicity and infectivity. Limitations of stem cell therapy include immunogenicity of cell, the potential for neoplasia, proper engineering of pure cardiac lineages and spatial non uniformity of implants. Regulating the level of expression to achieve optimal pacemaker rate is critical. Biological pacemaker needs an optimal cell mass and optimal cell-cell coupling for long term normal function. Research is ongoing to identify optimal cell numbers and coupling ratios needed to optimize the function of biological pacemakers.
            A major issue is duration of efficacy of biological pacemakers. The duration of pacemaker function in approaches using viruses depend on how long the viruses and resulting protein constructs survive in the host. To ensure long term function the appropriate delivery system in which the construct is effective for long periods must be identified. What will be the longevity and stability of next generation of pacemaker genes?
            The onset of pacemaker function after a pause following the last intrinsic beat is a critical factor. Can a pacemaker gene inserted into proximal conduction system create a functioning biological pacemaker which can drive the ventricle in demand mode when the sinus node signal fails? This requires proper engineering of genes. Considering the cell-cell coupling differences in gene therapy and stem cell therapy, the engineering of mutant genes will differ importantly between approaches.
            The autonomic responsiveness of biological pacemakers, the ideal site for implantation, the extent of recovery of diseased sinus node and the ideal construct to be preferred remain unanswered questions. None of the studies tested whether a biological pacemaker could be engineered into the ventricular conducting system. Will the functional characteristics of biological pacemakers compete with that of electronic units available?


1. Edelberg JM, Aird WC, Rosenberg RD. Enhancement of murine cardiac chronotropy by molecular transfer of the human b2 adrenergic receptor cDNA. J Clin Invest. 1998;101:337-343.

2. Miake J, Marban E, Nuss HB. Gene therapy: biological pacemaker created by gene transfer. Nature. 2002;419:132-133.

3. Potapova I, Plotnikov A, Lu Z. Human mesenchymal stem cells as a gene delivery system to crate cardiac pacemakers. Circulation research. 2004;952-959.

4. Zhou YY,Wang SQ, Zhu WZ,Chruscinski A, Kobilka BK, Ziman B,Wang S,Lakatta EG, Cheng H, Xiao PP. Culture and adenoviral infection of adult mouse cardiac myocytes;methods for cellular genetic physiology. Am J Physiol (Heart Circ physiol). 2000;279:H429-H436.

5. Hamm A, Krott N, Breibach I, Blindt R, Bosserfoff AK. Efficient transfection method for primary cells. Tissue ENG. 2002;8:235-245.

6. Di Francesco D. Pacemaker mechanism in cardiac tissue. Annu Rev Physiol. 1993; 55:455-472.

7.  Ludwig A, Zong X, Jeglitsch M. A family of hyperpolarisation activated mammalian cation channels. Nature 1998; 393:587-591.

8. Andreas Ludig et al. HCN channels, From genes to function. In: Douglas P Zipes, Jose Jalife, ed: Cardiac electrophysiology, From cell to bedside. Fourth edition. Saunders. pp. 59-65.

9. Moosmang S, Stieber J, Zong X, Biel M, Hofmann F, Ludwig A. Cellular expression and functional characterization of four hyperpolarization-activated pacemaker channels in cardiac and neuronal tissues. Eur J Biochem. 2001;268:1646-52

10. Biel M, Schneider A, Wahl C.  Cardiac HCN channels: structure, function, and modulation. Trends Cardiovasc Med. 2002;12:206-12.

11. Lopatin AN, Nichols CG.  Inward rectifiers in the heart: an update on I(K1). J Mol Cell Cardiol. 2001 ;33:625-38.

12. Nichols CG, Makhina EN, Pearson WL, Sha Q, Lopatin A. Inward rectification and implications for cardiac excitability. Circ Res. 1996 ;78(1):1-7.

13. Qu J, Plotnikov AN, Danilo P Jr, Shlapakova I, Cohen IS, Robinson RB, Rosen MR. Expression and function of a biological pacemaker in canine heart. Circulation. 2003; 107(8):1106-9.

14. Plotnikov AN, Sosunov EA, Qu J, Shlapakova IN, Anyukhovsky EP, Liu L, Janse MJ, Brink PR, Cohen IS, Robinson RB, Danilo P Jr, Rosen MR. Biological pacemaker implanted in canine left bundle branch provides ventricular escape rhythms that have physiologically acceptable rates. Circulation. 2004;109 (4):506-12.

Valiunas V, Weingart R, Brink PR.  Formation of heterotypic gap junction channels by connexins 40 and 43. Circ Res. 2000; 86(2):E42-9.

Home Page Current Issue List of Editors