Abstract
Normal rhythms originate in the sino-atrial node, a specialized cardiac tissue consisting of only a few thousands of nodal pacemaker cells. Malfunction of pacemaker cells due to diseases or aging leads to rhythm generation disorders (for example, bradycardias and sick-sinus syndrome (SSS)), which often necessitate the implantation of electronic pacemakers. Although effective, electronic devices are associated with such shortcomings as limited battery life, permanent implantation of leads, lead dislodging, the lack of autonomic responses and so on. Here, various gene- and cell-based approaches, with a particular emphasis placed on the use of pluripotent stem cells and the hyperpolarization-activated cyclic nucleotide-gated-encoded pacemaker gene family, that have been pursued in the past decade to reconstruct bio-artificial pacemakers as alternatives will be discussed in relation to the basic biological insights and translational regenerative potential.
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Acknowledgements
This work was supported by grants from the NIH—R01 HL72857, the CC Wong Foundation Stem Cell Fund and the Research Grant Council (T13-706/11 and 103544).
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Li, R. Gene- and cell-based bio-artificial pacemaker: what basic and translational lessons have we learned?. Gene Ther 19, 588–595 (2012). https://doi.org/10.1038/gt.2012.33
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DOI: https://doi.org/10.1038/gt.2012.33
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