All experimental procedures were conducted in accordance with the Animal Care Guidelines approved by University of Toronto Animal Use and Care Committee. Protocol for isolation of adult mouse cardiomyocytes was modified from Ackers-Johnson et al.14. Briefly, Sham-, 2-week TAC-, and 4-week TAC-operated CD1 mice hearts were perfused with EDTA buffer and perfusion buffer before being digested with warmed collagenase II buffer (250 units/mL; {"type":"entrez-nucleotide","attrs":{"text":"LS004176","term_id":"1321650548","term_text":"LS004176"}}LS004176, Worthington Biochemical Corp., Lakewood, NJ, USA). Following dissociation and washing, 3 stages of sedimentation were performed to remove the non-myocyte fraction before being suspended in culture media and plated on laminin-coated glass-bottom dishes. Cells were fixed 2 hours after plating and processed for immunofluorescence experiments.
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