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Epidermal plasminogen activator is abnormal in cutaneous lesions
P J Jensen1, J Baird, S Morioka
1Department of Dermatology, University of Pennsylvania, Philadelphia 19104.
The Journal of Investigative Dermatology
|June 1, 1988
Summary
Tissue plasminogen activator (tPA) is elevated in various skin diseases. This study examined plasminogen activator (PA) activity in normal and diseased skin, finding tPA predominant in lesions, suggesting its role in cutaneous pathology.
Area of Science:
- Dermatology
- Biochemistry
- Immunocytochemistry
Background:
- Plasminogen activator (PA) plays a role in tissue remodeling and degradation.
- Different forms of PA, including tissue-type PA (tPA) and urokinase-type PA (uPA), exist with distinct functions.
- The specific roles of PA in various cutaneous diseases are not fully understood.
Purpose of the Study:
- To investigate the role of plasminogen activator (PA) in the context of cutaneous diseases.
- To differentiate between tPA and uPA activity in normal and lesional skin.
- To immunocytochemically localize tPA in skin lesions of various dermatological conditions.
Main Methods:
- Biochemical assays to measure PA activity in skin samples.
- Immunocytochemical techniques using rabbit antibody specific for tPA.
- Analysis of skin biopsies from patients with pemphigus (benign chronic, vulgaris, foliaceous), bullous pemphigoid, and psoriasis.
Main Results:
- In normal human dermis, tPA is the predominant PA activity.
- In normal human epidermis, uPA is the predominant PA activity.
- In lesional epidermis from patients with various cutaneous diseases, tPA was the predominant PA activity, with a minor contribution from uPA.
- Immunocytochemical localization confirmed elevated tPA in lesions across diverse skin disorders.
Conclusions:
- Tissue plasminogen activator (tPA) is consistently elevated in cutaneous lesions regardless of etiology, pathology, or clinical presentation.
- The findings suggest a significant role for tPA in the pathogenesis of a wide range of skin diseases.
- Further research is warranted to elucidate the specific mechanisms by which tPA contributes to cutaneous disease.