Why the study?
Adult primary cardiac fibroblasts quickly differentiate into myofibroblasts in culture, necessitating their utilization directly after isolation or after a few passages.
This protocol provides a standardized method for isolating and culturing adult mouse cardiac fibroblasts, which are essential for in vitro studies of cardiac fibrosis and tissue homeostasis.
Enables reproducible cardiac fibroblast isolation for fibrosis models; leaves open translation to human disease.
Fibroblasts are dynamic cells of mesenchymal origin that regulate tissue homeostasis, extracellular matrix production, and acute wound healing. Fibroblasts respond to tissue injury and inflammation by differentiating into myofibroblasts and secreting extracellular matrix proteins. Fibroblasts are the principal mediators of the fibrotic response in all tissues and organs. Adult primary fibroblasts represent an essential tool for in vitro studies. Although they lack surface markers, fibroblasts are relatively easy to obtain and culture; primary fibroblasts are sensitive heterogeneous cell subpopulations with limited expansion potential and increased differentiation capacity. Adult primary fibroblasts fail to maintain an undifferentiated state ex vivo for long periods and quickly differentiate into myofibroblasts in culture, which necessitates the utilization of these cells either directly after isolation or after a few passages. Herein, we describe a detailed protocol for enzymatic isolation of primary cardiac fibroblasts from adult mouse hearts and their culture and expansion in a serum-containing culture medium.
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Almazloum et al. (2023) studied this question.
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