Skin-iDISCO+: An optimized tissue-clearing and labeling protocol for morphometric analysis of human cutaneous vasculature

Tissue clearing enables deep imaging of long biological structures using light microscopy approaches. Protocols such as iDISCO are not currently available for human skin. Here, we present Skin-iDISCO<sup>+</sup>, a tissue-clearing and labeling protocol for morphometric analysis of human cutaneous vasculature. We describe steps for processing and pre-treating tissue, immunostaining, clearing, and imaging using confocal and light-sheet fluorescence microscopy. We then detail procedures for the reconstruction of networks and the extraction of morphometric parameters of the skin vasculature. For complete details on the use and execution of this protocol, please refer to Renier et al.<sup>1</sup>.

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Publication Details

Journal
STAR Protocols
Published
2024-12-20
DOI
https://doi.org/10.1016/j.xpro.2024.103524
Citations
2
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.65
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article

Skin-iDISCO+: An optimized tissue-clearing and labeling protocol for morphometric analysis of human cutaneous vasculature

Muriel Cario, Jérémie Teillon, Hamid Rezvani, François Moisan et al.
2 citations
STAR Protocols
Cellular Mechanics and Interactions
0.65
article

Skin-iDISCO+: An optimized tissue-clearing and labeling protocol for morphometric analysis of human cutaneous vasculature

Muriel Cario, Jérémie Teillon, Hamid Rezvani, François Moisan, Sébastien Marais, L. Pechtimaldjian, Sébastien Dupichaud
article en
2 citations

Abstract

Tissue clearing enables deep imaging of long biological structures using light microscopy approaches. Protocols such as iDISCO are not currently available for human skin. Here, we present Skin-iDISCO<sup>+</sup>, a tissue-clearing and labeling protocol for morphometric analysis of human cutaneous vasculature. We describe steps for processing and pre-treating tissue, immunostaining, clearing, and imaging using confocal and light-sheet fluorescence microscopy. We then detail procedures for the reconstruction of networks and the extraction of morphometric parameters of the skin vasculature. For complete details on the use and execution of this protocol, please refer to Renier et al.<sup>1</sup>.

STAR ProtocolsVol. 6(1)
Université de Bordeaux (FR), Inserm (FR), Bordeaux Population Health (FR), Carl Zeiss (United States) (US)
Zero hunger
Openalex Percentile: Top 30%
Cellular Mechanics and Interactions
0.65
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