Two-photon microscopy of dermal innervation in a human re-innervated model of skin

When skin is injured, innervation can be severely disrupted. The subsequent re‐innervation processes are poorly understood notably because of the inability to image the full meandering course of nerves with their ramifications and endings from histological slices. In this letter, we report on two‐ph...

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Veröffentlicht in:Experimental dermatology 2013-04, Vol.22 (4), p.290-291
Hauptverfasser: Sevrain, David, Le Grand, Yann, Buhé, Virginie, Jeanmaire, Christine, Pauly, Gilles, Carré, Jean-Luc, Misery, Laurent, Lebonvallet, Nicolas
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container_end_page 291
container_issue 4
container_start_page 290
container_title Experimental dermatology
container_volume 22
creator Sevrain, David
Le Grand, Yann
Buhé, Virginie
Jeanmaire, Christine
Pauly, Gilles
Carré, Jean-Luc
Misery, Laurent
Lebonvallet, Nicolas
description When skin is injured, innervation can be severely disrupted. The subsequent re‐innervation processes are poorly understood notably because of the inability to image the full meandering course of nerves with their ramifications and endings from histological slices. In this letter, we report on two‐photon excitation fluorescence (TPEF) microscopy of entire human skin explants re‐innervated by rodent sensory neurons labelled with the styryl dye FM1‐43. TPEF imaging of nerve fibres to a depth up to roughly 300 μm within the dermis was demonstrated, allowing three‐dimensional reconstruction of the neural tree structure. Endogenous second‐harmonic imaging of type I fibrillar collagen was performed in parallel to TPEF imaging using the same nonlinear microscope, revealing the path of the nerves through the dermis.
doi_str_mv 10.1111/exd.12108
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The subsequent re‐innervation processes are poorly understood notably because of the inability to image the full meandering course of nerves with their ramifications and endings from histological slices. In this letter, we report on two‐photon excitation fluorescence (TPEF) microscopy of entire human skin explants re‐innervated by rodent sensory neurons labelled with the styryl dye FM1‐43. TPEF imaging of nerve fibres to a depth up to roughly 300 μm within the dermis was demonstrated, allowing three‐dimensional reconstruction of the neural tree structure. 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The subsequent re‐innervation processes are poorly understood notably because of the inability to image the full meandering course of nerves with their ramifications and endings from histological slices. In this letter, we report on two‐photon excitation fluorescence (TPEF) microscopy of entire human skin explants re‐innervated by rodent sensory neurons labelled with the styryl dye FM1‐43. TPEF imaging of nerve fibres to a depth up to roughly 300 μm within the dermis was demonstrated, allowing three‐dimensional reconstruction of the neural tree structure. 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subjects Animals
Cellular Biology
Coculture Techniques
Dermis
Dermis - innervation
Fluorescent Dyes
FM1-43
Humans
Imaging, Three-Dimensional
Life Sciences
Microscopy, Fluorescence, Multiphoton
Models, Neurological
Nerve Regeneration
neuron
Optics
Physics
Pyridinium Compounds
Quaternary Ammonium Compounds
Rats
Rats, Wistar
re-innervation
Sensory Receptor Cells
Sensory Receptor Cells - physiology
Skin
Skin - injuries
Skin - innervation
styryl dye
two-photon microscopy
title Two-photon microscopy of dermal innervation in a human re-innervated model of skin
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