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Rapid Generation of Primary Murine Melanocyte and Fibroblast Cultures
Published on: June 26, 2019
Protocol for the generation, viability assessment, and downstream processing of murine precision-cut skin slices
Nicolas Perrard1, Manel Jendoubi2, Blanche Daunou2
1University of Lille, Inserm, CHU Lille, U1286 - INFINITE - Institute for Translational Research in Inflammation, 59000 Lille, France; Department of Internal Medicine and Clinical Immunology, CHU Lille, 59000 Lille, France.
Abstract:
Precision-cut tissue slices (PCTS) are an ex vivo model of viable organ sections widely used for therapeutic screening, toxicity assessment, and infection modeling. Here, we present a protocol for the generation, viability assessment, and downstream processing of murine Precision-cut Skin Slices (PCSS). We describe steps for preparing and agarose embedding skin samples, generating PCSS, maintaining them in culture, detecting lactate dehydrogenase (LDH), and quantifying ATP. We then detail procedures for RNA/protein extraction, the quantification of PCSS homogenates, and histological and TUNEL analysis of PCSS.

