Establishment of Transgene‐Free Porcine Induced Pluripotent Stem Cells

Abstract

Although protocols to generate authentic transgene‐free mouse and human induced pluripotent stem cells (iPSCs) are now well established, standard methods for reprogramming porcine somatic cells still suffer from low efficiency and transgene retention. The Basic Protocol describes reprogramming procedures to establish transgene‐free porcine iPSCs (PiPSCs) from porcine fibroblasts. This method uses episomal plasmids encoding POU5F1, SOX2, NANOG, KLF4, SV40LT, c‐MYC, LIN28A, and microRNA‐302/367, combined with an optimized medium, to establish PiPSC lines. Support protocols describe the establishment and characterization of clonal PiPSC lines, as well as the preparation of feeder cells and EBNA1 mRNA. This optimized, step‐by‐step approach tailored to this species enables the efficient derivation of PiPSCs in ∼4 weeks. The establishment of transgene‐free PiPSCs provides a new and valuable model for studies of larger mammalian species’ development, disease, and regenerative biology. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC.Basic Protocol: Reprogramming of porcine fibroblasts with episomal plasmidsSupport Protocol 1: Preparation of mouse embryonic fibroblasts for feeder layerSupport Protocol 2: Preparation of in vitro–transcribed EBNA1 mRNASupport Protocol 3: Establishment of clonal porcine induced pluripotent stem cell (PiPSC) linesSupport Protocol 4: PiPSC characterization: Genomic DNA PCR and RT‐PCRSupport Protocol 5: PiPSC characterization: Immunostaining