Artificial biological pacemakers were developed and tested in canine
ventricles. Next steps will require obtaining oscillations sensitive to
external regulations, and robust with respect to long term drifts of expression
levels of pacemaker currents and gap junctions. We introduce mathematical
models intended to be used in parallel with the experiments.
The models describe human mesenchymal stem cells ({\it hMSC}) transfected
with HCN2 genes and connected to myocytes. They are intended to mimic
experiments with oscillation induction in a cell pair, in cell culture and in
the cardiac tissue. We give examples of oscillations in a cell pair, in a 1 dim
cell culture, and oscillation dependence on number of pacemaker channels per
cell and number of gap junctions. The models permit to mimic experiments with
levels of gene expressions not achieved yet, and to predict if the work to
achieve this levels will significantly increase the quality of oscillations.
This give arguments for selecting the directions of the experimental work