A three-dimensional atlas of human dermal leukocytes, lymphatics, and blood vessels
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Updated: May 4, 2026

Three-Dimensional Imaging of the Vertebral Lymphatic Vasculature and Drainage using iDISCO+ and Light Sheet Fluorescence Microscopy
Published on: May 22, 2020
Xiao-Nong Wang1, Naomi McGovern1, Merry Gunawan1
1Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK.
Insights
Skin immune cells, including dendritic cells (DCs) and macrophages (Mφ), organize in distinct dermal layers. Whole-mount imaging reveals their spatial distribution and behavior in lymphatics, offering insights into skin immunity.
Area of Science:
- Immunology
- Dermal Micro-anatomy
- Skin Immune System
Background:
- The spatial organization of dendritic cells (DCs), macrophages (Mφ), and T cells in the skin's immune system is not well understood.
- Previous studies using cross-sections may underestimate the true extent of dermal leukocytes.
Purpose of the Study:
- To characterize the three-dimensional distribution of immune cells within the human dermis.
- To investigate the in situ differences between DCs and Mφ and their organization relative to blood and lymphatic vessels.
Main Methods:
- Four-channel whole-mount immunofluorescence staining of human dermis.
- 3D imaging to visualize CD31(+) blood capillaries, LYVE-1(+) lymphatics, CD11c(+) myeloid DCs, FXIIIa(+) Mφ, and lymphocytes.
Main Results:
- DCs form the superficial dermal layer (0-20 µm), Mφ are deeper (40-60 µm), and lymphocytes are distributed throughout (0-60 µm).
- DCs, T cells, and Mφ form perivascular sheaths; apical dermis contains significantly more myeloid DCs than previously thought.
- Dermal DCs rapidly enter lymphatics ex vivo, while Mφ remain fixed.
Conclusions:
- This study elucidates the micro-anatomy of dermal leukocytes and their functional organization in normal and diseased skin.
- The findings highlight the dynamic nature of DCs in lymphatic uptake and provide a detailed map of skin immune cell architecture.
Abstract:
Dendritic cells (DCs), macrophages (Mφ), and T cells are major components of the skin immune system, but their interstitial spatial organization is poorly characterized. Using four-channel whole-mount immunofluorescence staining of the human dermis, we demonstrated the three-dimensional distribution of CD31(+) blood capillaries, LYVE-1(+) lymphatics, discrete populations of CD11c(+) myeloid DCs, FXIIIa(+) Mφ, and lymphocytes. We showed phenotypic and morphological differences in situ between DCs and Mφ. DCs formed the first dermal cellular layer (0-20 microm beneath the dermoepidermal junction), Mφ were located deeper (40-60 microm), and CD3(+) lymphocytes were observed throughout (0-60 microm). Below this level, DCs, T cells, and the majority of Mφ formed stable perivascular sheaths. Whole-mount imaging revealed the true extent of dermal leukocytes previously underestimated from cross-section views. The total area of apical dermis (0-30 microm) contained approximately 10-fold more myeloid DCs than the entire blood volume of an average individual. Surprisingly, <1% of dermal DCs occupied lymphatics in freshly isolated skin. Dermal DCs rapidly accumulated within lymphatics, but Mφ remained fixed in skin explants cultured ex vivo. The leukocyte architecture observed in normal skin was distorted in inflammation and disease. These studies illustrate the micro-anatomy of dermal leukocytes and provide further insights into their functional organization.
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