Key result
Antegrade perfusion enables simultaneous isolation of ventricular and atrial myocytes plus fibroblasts from mouse hearts.
Why the study?
Isolating viable individual cardiomyocytes from mouse hearts is technically challenging due to the small size and skill required for traditional retrograde perfusion methods.
May streamline multi-cell isolation from single mouse hearts; leaves open its impact on preclinical efficiency and reproducibility.
In basic research using mouse heart, isolating viable individual cardiomyocytes is a crucial technical step to overcome. Traditionally, isolating cardiomyocytes from rabbits, guinea pigs or rats has been performed via retrograde perfusion of the heart with enzymes using a Langendorff apparatus. However, a high degree of skill is required when this method is used with a small mouse heart. An antegrade perfusion method that does not use a Langendorff apparatus was recently reported for the isolation of mouse cardiomyocytes. We herein report a complete protocol for the improved antegrade perfusion of the excised heart to isolate individual heart cells from adult mice (8 - 108 weeks old). Antegrade perfusion is performed by injecting perfusate near the apex of the left ventricle of the excised heart, the aorta of which was clamped, using an infusion pump. All procedures are carried out on a pre-warmed heater mat under a microscope, which allows for the injection and perfusion processes to be monitored. The results suggest that ventricular and atrial myocytes, and fibroblasts can be well isolated from a single adult mouse simultaneously.
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Omatsu‐Kanbe et al. (2021) studied Cardiomyocyte isolation. Antegrade perfusion method was evaluated on Isolation of individual heart cells. An antegrade perfusion method successfully isolated ventricular and atrial myocytes, and fibroblasts from a single adult mouse simultaneously.
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