Role of NF-κB in the pathogenesis of psoriasis elucidated by its staining in skin biopsy specimens
Autor: | Janmeet S. Kulaar, Nikhil Moorchung, Tanu Tripathi, Biju Vasudevan, Vibha Dutta, Manas Chatterjee |
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Rok vydání: | 2013 |
Předmět: |
Adult
Male Pathology medicine.medical_specialty Adolescent Biopsy Dermatology Proinflammatory cytokine Pathogenesis Basal (phylogenetics) Young Adult Psoriasis Medicine Humans Prospective Studies Aged Skin integumentary system medicine.diagnostic_test Epidermis (botany) Staining and Labeling business.industry NF-kappa B Middle Aged medicine.disease Staining Dermal papillae medicine.anatomical_structure Skin biopsy Female business |
Zdroj: | International journal of dermatology. 53(5) |
ISSN: | 1365-4632 |
Popis: | Background NF-κB is a transcription factor belonging to the Re1 family, and it regulates the activity of a large number of proinflammatory genes. Its role in psoriasis, which is a prototype chronic inflammatory disease, is therefore expected to be considerable. It has been found that many of the triggering factors for psoriasis initiate inflammation by activation of NF-κB. Methods Skin biopsies of 74 psoriatic cases were studied for the grade of NF-κB staining. They were then correlated with the histopathological indices of severity, especially epidermal hyperplasia and inflammatory infiltrate. Results Epidermal nuclear positivity for NF-κB correlated with the grade of epidermal hyperplasia (P = 0.043). There was a significant correlation between grade of basal cell positivity of NF-κB and inflammatory infiltrate (P = 0.004). Lymphocyte staining showed a strong correlation with epidermal and basal cell staining pattern for NF-κB (P = 0.004 and 0.003, respectively). There was, however, no correlation of lymphocyte staining with any histopathological parameter. There was also a peculiar propensity for NF-κB to show a positive nuclear stain at the tips of dermal papillae. Conclusions The study has demonstrated that translocation of NF-κB in the epidermis and basal cells is responsible for two of the key pathological features of psoriasis, epidermal hyperplasia, and inflammation. We have postulated that translocation of NF-κB in lymphocytes, in psoriatic skin leads to NF-κB translocation in the epidermis and basal cells. NF-κB is therefore likely to be one of the key molecules in the pathogenesis of psoriasis. |
Databáze: | OpenAIRE |
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