An efficient method for immortalizing mouse embryonic fibroblasts

Abstract

Mouse embryonic fibroblasts (MEFs) derived from genetically modified mice are a valuable resource for studying gene function and regulation. The MEF system can also be combined with rescue studies to characterize the function of mutant genes/proteins, such as disease-causing variants. However, primary MEFs undergo senescence soon after isolation and passaging, making long-term genetic manipulations difficult. Previously described methods for MEF immortalization are often inefficient or alter the physiological properties of the cells. Here, we describe an optimized protocol for immortalizing MEFs via CRISPR-mediated deletion of theTp53gene. This method is highly efficient and consistently generates immortalized MEFs, or iMEFs, within 14 days. Importantly, iMEFs closely resemble the parent cell populations, and individual iMEFs can be cloned and expanded for subsequent genetic manipulation and characterization. We envision that this protocol can be adopted to immortalize other mouse primary cell types.Key FeaturesCRISPR-based knockout of theTp53gene enables efficient immortalization of mouse embryonic fibroblasts (MEFs) in under 2 weeks.Immortalization requires a Neon electroporator or another comparable electroporation system to transfect cells with theTp53CRISPR constructs.