Key result
A protocol combining enzymatic digestion and mechanical dissociation consistently yields isolated adult mouse atrial cardiomyocytes suitable for characterizing cellular electrophysiology.
Why the study?
Isolating adult mouse atrial cardiomyocytes for patch-clamp experiments is critical to understanding cellular electrophysiology in healthy and diseased atrial myocardium, requiring a consistent and reliable isolation method.
This paper provides a detailed, reliable protocol for isolating adult mouse atrial cardiomyocytes for use in cellular electrophysiology studies.
The electrophysiological properties of atrial myocytes importantly affect overall cardiac function. Alterations in the underlying ionic currents responsible for the action potential can cause pro-arrhythmic substrates that underlie arrhythmias, such as atrial fibrillation, which are highly prevalent in many conditions and disease states. Isolating adult mouse atrial cardiomyocytes for use in patch-clamp experiments has greatly advanced our knowledge and understanding of the cellular electrophysiology in the healthy atrial myocardium and in the setting of atrial pathophysiology. In addition, studies using genetic mouse models have elucidated the role of a vast array of proteins in regulating atrial electrophysiology. Here we provide a detailed protocol for the isolation of cardiomyocytes from the atrial appendages of adult mice using a combination of enzymatic digestion and mechanical dissociation of these tissues. This approach consistently and reliably yields isolated atrial cardiomyocytes that can then be used to characterize cellular electrophysiology by measuring action potentials and ionic currents in patch-clamp experiments under a number of experimental conditions.
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Jansen et al. (2019) studied Atrial electrophysiology. Enzymatic digestion and mechanical dissociation was evaluated on Yield of isolated atrial cardiomyocytes. A protocol combining enzymatic digestion and mechanical dissociation consistently yields isolated adult mouse atrial cardiomyocytes suitable for characterizing cellular electrophysiology.
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