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VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations
René Hägerling, Dominik Drees, Aaron Scherzinger, Cathrin Dierkes, Silvia Martin-Almedina, Stefan Butz, Kristiana Gordon, Michael Schäfers, Klaus Hinrichs, Pia Ostergaard, Dietmar Vestweber, Tobias Goerge, Sahar Mansour, Xiaoyi Jiang, Peter S. Mortimer, Friedemann Kiefer
René Hägerling, Dominik Drees, Aaron Scherzinger, Cathrin Dierkes, Silvia Martin-Almedina, Stefan Butz, Kristiana Gordon, Michael Schäfers, Klaus Hinrichs, Pia Ostergaard, Dietmar Vestweber, Tobias Goerge, Sahar Mansour, Xiaoyi Jiang, Peter S. Mortimer, Friedemann Kiefer
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Clinical Research and Public Health Dermatology Vascular biology

VIPAR, a quantitative approach to 3D histopathology applied to lymphatic malformations

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Abstract

BACKGROUND. Lack of investigatory and diagnostic tools has been a major contributing factor to the failure to mechanistically understand lymphedema and other lymphatic disorders in order to develop effective drug and surgical therapies. One difficulty has been understanding the true changes in lymph vessel pathology from standard 2D tissue sections. METHODS. VIPAR (volume information-based histopathological analysis by 3D reconstruction and data extraction), a light-sheet microscopy–based approach for the analysis of tissue biopsies, is based on digital reconstruction and visualization of microscopic image stacks. VIPAR allows semiautomated segmentation of the vasculature and subsequent nonbiased extraction of characteristic vessel shape and connectivity parameters. We applied VIPAR to analyze biopsies from healthy lymphedematous and lymphangiomatous skin. RESULTS. Digital 3D reconstruction provided a directly visually interpretable, comprehensive representation of the lymphatic and blood vessels in the analyzed tissue volumes. The most conspicuous features were disrupted lymphatic vessels in lymphedematous skin and a hyperplasia (4.36-fold lymphatic vessel volume increase) in the lymphangiomatous skin. Both abnormalities were detected by the connectivity analysis based on extracted vessel shape and structure data. The quantitative evaluation of extracted data revealed a significant reduction of lymphatic segment length (51.3% and 54.2%) and straightness (89.2% and 83.7%) for lymphedematous and lymphangiomatous skin, respectively. Blood vessel length was significantly increased in the lymphangiomatous sample (239.3%). CONCLUSION. VIPAR is a volume-based tissue reconstruction data extraction and analysis approach that successfully distinguished healthy from lymphedematous and lymphangiomatous skin. Its application is not limited to the vascular systems or skin. FUNDING. Max Planck Society, DFG (SFB 656), and Cells-in-Motion Cluster of Excellence EXC 1003.

Authors

René Hägerling, Dominik Drees, Aaron Scherzinger, Cathrin Dierkes, Silvia Martin-Almedina, Stefan Butz, Kristiana Gordon, Michael Schäfers, Klaus Hinrichs, Pia Ostergaard, Dietmar Vestweber, Tobias Goerge, Sahar Mansour, Xiaoyi Jiang, Peter S. Mortimer, Friedemann Kiefer

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Figure 2

Light-sheet microscopy–based analysis of healthy and diseased skin biopsies reveals lymph vessel defects that are unrecognizable in microtome sections.

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Light-sheet microscopy–based analysis of healthy and diseased skin biops...
(A–C) Immunohistological detection of vascular markers in microtome sections of healthy control (A) and patient (B and C) lower limb skin biopsies. ESAM1, endothelial marker; PDPN, LYVE1, and PROX1, lymphatic-specific endothelial markers. Lumenized blood (yellow arrows) and lymphatic vessels (white arrowheads) are indicated. Dashed line depicts the border between epidermis (indicated by red asterisks) and dermis. Scale bars: 100 μm. (D–L) Maximum intensity projections of image stacks derived by light-sheet microscopy (UltraMicroscope II) of whole-mount immunostained control (D, G, and J) and patient skin biopsies (E, F, H, I, K, and L). Image stacks were rendered using the volume visualization framework Voreen. Detected antigens and respective colors are indicated. (D and F) Lymphatic valve areas (identified by high PROX1 expression) are marked by white arrows; valve areas were absent in patient biopsies (E and F). Specimens are depicted such that the epidermal layer is located on the top of the picture (red asterisks). Note acanthosis and hyperkeratosis in patient biopsy (B and C). Scale bars: 100 μm.

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