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Updated: Aug 9, 2026

Generation and Culturing of Primary Human Keratinocytes from Adult Skin
Published on: December 22, 2017
Adhesion of epidermal Langerhans cells to keratinocytes mediated by E-cadherin
A Tang1, M Amagai, L G Granger
1Dermatology Branch, National Cancer Institute, Bethesda, Maryland 20892.
Insights
Langerhans cells (LC) in the skin use E-cadherin to stick to keratinocytes (KC). Reduced E-cadherin on cultured LC may explain their migration from skin to lymph nodes.
Area of Science:
- Immunology
- Dermatology
- Cell Biology
Background:
- Langerhans cells (LC) are key immune cells in the epidermis, acting as accessory cells.
- Epidermal repopulation relies on bone marrow-derived LC progenitors due to LC's limited self-renewal.
- LC migrate from skin to lymph nodes upon antigen exposure, but mechanisms remain unclear.
Purpose of the Study:
- To investigate the role of Langerhans cell-keratinocyte (LC-KC) interactions in LC trafficking.
- To characterize the molecular mechanisms underlying LC adhesion to epidermal cells.
Main Methods:
- Analysis of cadherin expression on fresh and cultured murine LC.
- In vitro assessment of LC-KC adhesion.
- Comparison of E-cadherin levels and adhesion affinity between fresh and cultured LC.
Main Results:
- Fresh murine LC express cadherins and adhere to keratinocytes (KC) via E-cadherin.
- Cultured LC, potentially resembling migrated cells, show reduced E-cadherin expression.
- Cultured LC exhibit decreased adhesion affinity for KC compared to fresh LC.
Conclusions:
- E-cadherin expression on LC appears crucial for their retention within the epidermis.
- Cadherins may play a significant, previously unrecognized role in leukocyte-epithelial interactions.
- Understanding LC-KC adhesion mechanisms offers insights into immune cell trafficking and retention.
Abstract:
Langerhans cells (LC) are the principal accessory cells present in epidermis. Because LC have limited capacity for self-renewal, epidermis is continually repopulated by as-yet uncharacterized bone marrow-derived LC progenitors. In addition, although LC persist in epidermis for extended periods, LC are induced to migrate from skin to regional lymph nodes after antigen exposure. To begin to elucidate mechanisms involved in LC trafficking, we characterized LC-keratinocyte (KC) interactions. Here we report that fresh murine LC express cadherins, and that LC adhere to KC in vitro through E-cadherin. Cultured LC (which may bear a phenotypic and functional relationship to LC that have migrated to lymph nodes) express lower levels of E-cadherin and exhibit decreased affinity for KC. These results suggest that expression of E-cadherin by LC promotes persistence of these cells in epidermis, and that cadherins may play important and unanticipated roles in interactions between leukocytes and epithelia.
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