Related Experiment Video
Updated: Aug 8, 2026

Adhesion Frequency Assay for In Situ Kinetics Analysis of Cross-Junctional Molecular Interactions at the Cell-Cell Interface
Published on: November 2, 2011
Differential cell surface distribution of adhesion molecules demonstrated by immuno-scanning electron microscopy
1Department of Dermatology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
Insights
Immuno-gold labeling reveals distinct expression patterns of ICAM-1 and HLA-DR in mycosis fungoides (MF) and lichenoid reaction (LR). These differences in immune molecule distribution explain the unique histological features of each condition.
Area of Science:
- Dermatopathology
- Immunohistochemistry
- Cellular Biology
Background:
- Mycosis fungoides (MF) and lichenoid reaction (LR) are distinct inflammatory skin conditions with overlapping clinical and histological features.
- Understanding the molecular mechanisms underlying their pathogenesis is crucial for accurate diagnosis and treatment.
Purpose of the Study:
- To investigate the differential expression of intercellular adhesion molecule-1 (ICAM-1), leukocyte function-associated antigen-1 (LFA-1), and human leukocyte antigen-DR (HLA-DR) in MF and LR.
- To correlate these molecular findings with the characteristic histological patterns of epidermotropism and band-like infiltrate.
Main Methods:
- Scanning electron microscopy (SEM) combined with immuno-gold labeling was employed.
- Expression patterns of ICAM-1, LFA-1, and HLA-DR were analyzed on epidermal keratinocytes and dermal infiltrates in MF and LR lesions.
Main Results:
- In MF, ICAM-1 was clustered at keratinocyte junctions, and HLA-DR was continuously expressed along keratinocyte borders. LFA-1 was found on infiltrates, many co-expressing ICAM-1.
- In LR, ICAM-1 and HLA-DR were sparsely expressed on the epidermal undersurface, while infiltrates expressed LFA-1.
- Distinct ICAM-1 distribution in MF correlates with LFA-1-bearing cell migration into keratinocyte interspaces (epidermotropism) and aggregation (microabscess formation).
Conclusions:
- Differential expression of ICAM-1 and HLA-DR molecules contributes to the distinct histological features observed in MF and LR.
- The findings provide a molecular basis for understanding epidermotropism in MF and the band-like infiltrate in LR.
- Targeting these adhesion molecules may offer therapeutic potential in managing these skin conditions.
Abstract:
Scanning electron microscopy with immuno-gold labeling revealed that epidermal keratinocytes expressed ICAM-1 and HLA-DR molecules on their surfaces in patterns that differed in mycosis fungoides (MF) and lichenoid reaction (LR). ICAM-1 molecules, visualized as deposits of gold particles, were present as clusters adjacent to the junctions interconnecting the keratinocytes of MF lesions. LFA-1 molecules were seen as granules on the surfaces of all infiltrates, most of which also expressed ICAM-1. HLA-DR molecules were seen continuously along the borders of the individual keratinocytes. In LR, ICAM-1 and HLA-DR were expressed only sparsely on the undersurface of the epidermis, whereas the infiltrates expressed LFA-1 molecules on their surfaces. These findings may explain the differing histological features of MF and LR: ICAM-1 molecules present on the intercellular junctions of MF epidermis lead the LFA-1-bearing cells to migrate into the interspaces of the keratinocytes, thus producing "epidermotropism". These cells aggregate by means of co-expressed ICAM-1 to thus produce the appearance of a "microabscess". In LR, on the other hand, the minimal expression of ICAM-1 on the epidermal undersurface leaves most infiltrates within the dermis, thus producing a "band-like infiltrate" beneath the epidermis.
More Related Videos
Related Concept Videos
Cell Adhesion Molecules - Types and Functions
CAM Families
The Integrin family of proteins is primarily involved in a...
Immunoglobulin-like Cell Adhesion Molecules
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
Immunogold Electron Microscopy

