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Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Differences in low density lipoprotein receptor expression in the suprabasal layer of normal and psoriatic epidermis
M Mommaas1, J Tada, M C Wijsman
1Department of Dermatology, University Hospital Leiden, The Netherlands.
Insights
The low-density lipoprotein (LDL) receptor is more abundant on the surface of suprabasal cells in psoriasis skin compared to normal skin. This increased expression may be linked to the hyperproliferative state characteristic of psoriasis.
Area of Science:
- Dermatology
- Cell Biology
- Biochemistry
Background:
- Previous studies linked low-density lipoprotein (LDL) binding to keratinocyte differentiation in normal and psoriatic epidermis.
- The role of the LDL receptor in this binding phenomenon required further investigation.
Purpose of the Study:
- To determine the involvement and localization of the LDL receptor in normal versus psoriatic epidermis.
- To investigate the relationship between LDL receptor expression and keratinocyte differentiation state.
Main Methods:
- Immunoelectronmicroscopy was employed using a monoclonal anti-LDL receptor antibody.
- Biopsy specimens of normal and psoriatic skin were processed and labeled with antibodies conjugated to colloidal gold.
Main Results:
- LDL receptors were evenly distributed between the cell surface and cytoplasm in basal cells of both normal and psoriatic epidermis.
- Suprabasal cells in normal epidermis showed fewer LDL receptors compared to basal cells.
- Psoriatic suprabasal cells exhibited increased LDL receptor numbers relative to basal cells, with a majority located on the cell surface.
Conclusions:
- Psoriatic suprabasal cells display a higher expression of LDL receptors compared to normal suprabasal cells.
- The predominant cell surface localization of LDL receptors in psoriatic suprabasal cells suggests a connection to the disorder's hyperproliferative state.
Abstract:
Previous morphological experiments on the distribution of binding sites for low density lipoprotein (LDL) on normal and psoriatic epidermis in situ, done with the LDL-gold technique [Mommaas-Kienhuis AM, et al. J Invest Dermatol 89: 513-517, 1987.] showed an unequivocal correlation between the ability to bind LDL-gold complexes and the state of keratinocyte differentiation. To determine the involvement of the LDL receptor in this phenomenon, we applied immunoelectronmicroscopical methods in conjunction with a monoclonal anti-LDL receptor antibody. Biopsy specimens of normal and psoriasis skin were fixed before being embedded in Lowicryl K4M. Ultrathin sections were incubated first with the anti-LDL receptor antibody, and then with a second antibody conjugated to colloidal gold. On basal cells of both normal and psoriatic epidermis the LDL receptor was distributed evenly between the cell surface and the cytoplasm. No obvious differences in the density of LDL receptors were observed. However, cells from the suprabasal layer showed two striking differences in the localization of the LDL receptor: 1) normal epidermis showed fewer LDL receptor molecules, whereas in psoriasis epidermis the number increased relative to those on basal cells; and 2) in normal suprabasal cells most of the LDL receptors were located inside the cell, but in psoriasis the majority was found on the cell surface. Both phenomena are discussed and we postulate that the higher expression of LDL receptors in psoriasis suprabasal cells and the high expression of the receptor on the cell surface is connected with the hyperproliferative state of the disorder.
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