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Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Thrombomodulin expression on dermal cells in normal and psoriatic skin
T Cuzzi-Maya1, R Sidbury, W L Epstein
1Departamento de Patologia, Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, RJ, Brasil. tcmaya@openlink.com.br
Insights
Researchers identified a distinct subset of dermal cells expressing thrombomodulin in human skin. These cells, distinct from dermal dendrocytes and macrophages, may play a role in tissue repair and regulating blood clotting.
Area of Science:
- Dermatology
- Immunohistochemistry
- Cell Biology
Background:
- Dermal cells with dendritic morphology are diverse and identified by specific cell markers.
- Thrombomodulin is a cell surface protein involved in regulating blood coagulation.
Purpose of the Study:
- To characterize the morphology and tissue distribution of thrombomodulin-expressing dermal cells in normal and psoriatic skin.
- To investigate the relationship between thrombomodulin+ dermal cells and other dermal cell populations like dermal dendrocytes and macrophages.
Main Methods:
- Histological analysis of skin sections from normal arm, scalp, and psoriatic lesions.
- Immunohistochemistry using a monoclonal antibody against thrombomodulin.
- Double staining with antibodies for factor XIIIa, CD34, and CD68 in scalp biopsies.
Main Results:
- Thrombomodulin+ dermal cells exhibited distinct morphologies and distributions in normal arm, scalp, and psoriatic skin.
- These cells were negative for factor XIIIa, CD34, and CD68, suggesting they represent a unique dermal cell subset.
- Thrombomodulin+ dermal cells were often found in proximity to factor XIIIa+ dermal dendrocytes.
Conclusions:
- Thrombomodulin+ dermal cells represent a distinct subset of dermal cells, potentially involved in tissue repair.
- These cells may cooperate with dermal dendrocytes to regulate extravascular thrombin homeostasis in skin.
- Understanding these cells offers insights into dermal biology and wound healing processes.
Abstract:
The various subsets of dermal cells with a dendritic appearance can be identified by phenotypic differences in cell markers. We report on the morphology and tissue distribution of dermal cells detected with a monoclonal antibody against thrombomodulin in histological sections of normal arm and scalp skin and psoriatic skin. Double staining with antibodies to factor XIIIa, CD34 and CD68 was also employed in scalp biopsies to elucidate the relationship between thrombomodulin+ dermal cells and dermal dendrocytes and macrophages described by others. Thrombomodulin+ dermal cells in normal arm skin had little cytoplasm with fine branched dendrites and tended to be localized just beneath the epidermis. In scalp skin these cells had longer, more numerous dendrites and were distributed in the papillae and perivascular adventitial dermis primarily in the upper and central reticular dermis. In psoriatic skin, thrombomodulin+ dermal cells had an increased cytoplasmic volume with stout, less branched dendrites and appeared in the papillae and among inflammatory cells. Dermal cells detectable by thrombomodulin expression were factor XIIIa-, CD34- and CD68-, and seemed to represent a distinct subset of dermal cells which may function in tissue repair. However, thrombomodulin+ dermal cells and factor XIIIa+ dendrocytes were frequently seen close together and could act cooperatively to regulate extravascular thrombin homeostasis in both normal and pathological dermal environments.
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