Skin Whole‐Mount Immunofluorescent Staining Protocol, 3D Visualization, and Spatial Image Analysis

Author:

Schmidt Alfonso J.12,Wright Graham D.3,Ronchese Franca2,Price Kylie M.12

Affiliation:

1. Hugh Green Cytometry Centre Wellington New Zealand

2. Malaghan Institute of Medical Research Wellington New Zealand

3. A*STAR Microscopy Platform, Research Support Centre, Agency for Science Technology & Research (A*STAR) 30 Biopolis Street, #05‐02D Matrix 138671 Singapore

Abstract

AbstractThe use of polychromatic immunofluorescent staining on whole‐mount skin enables cell type characterization and aids in the delineation of the physiological and immunological strategies used by the skin to combat pathogens. Using whole‐mount skin for polychromatic immunofluorescent staining removes the need for histological sectioning and enables the visualization of anatomical structures and immune cell types in three dimensions. Here we present a detailed protocol for immunostaining with fluorescence‐conjugated primary antibodies in whole‐mount skin to reveal structural landmarks and specific immune cell types using confocal laser scanning microscopy (CLSM) (Basic Protocol 1). The optimized staining panel reveals structural features such as blood vessels (CD31 antibody) and the lymphatic network (LYVE‐1 antibody), in combination with MHCII antibodies for antigen‐presenting cells (APCs), CD64 for macrophages and monocytes, CD103 for dendritic epidermal T cells (DETC), and CD326 for Langerhans cells (LC). Basic Protocol 2 describes image visualization pipelines using open‐source software (ImageJ/FIJI), enabling four visualization options (z‐projections, orthogonal views, 3D visualization, and animation). Basic Protocol 3 describes a quantitative analysis pipeline using CellProfiler to characterize the spatial relationship between cell types using mathematical indices such as Spatial Distribution Index (SDI), Neighborhood Frequency (NF), and Normalized Median Evenness (NME). These protocols will enable researchers to stain, record, analyze, and interpret data from whole‐mount skin using commercially available reagents in a CLSM‐equipped laboratory and freely available analysis software. © 2023 Wiley Periodicals LLC.Basic Protocol 1: Immunofluorescent staining and imaging for whole‐mount mouse skinBasic Protocol 2: File rendering and visualization using FIJIBasic Protocol 3: Spatial image analysis using CellProfiler

Publisher

Wiley

Subject

Medical Laboratory Technology,Health Informatics,General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

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