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Changes in nuclear morphology and chromatin texture of basal keratinocytes in melasma
Author(s) -
Brianezi G.,
Handel A.C.,
Schmitt J.V.,
Miot L.D.B.,
Miot H.A.
Publication year - 2015
Publication title -
journal of the european academy of dermatology and venereology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 107
eISSN - 1468-3083
pISSN - 0926-9959
DOI - 10.1111/jdv.12453
Subject(s) - medicine , melasma , dermatology , basal (medicine) , morphology (biology) , texture (cosmology) , chromatin , zoology , artificial intelligence , genetics , dna , biology , insulin , computer science , image (mathematics)
Background The pathogenesis of melasma and the role of keratinocytes in disease development and maintenance are not completely understood. Dermal abnormalities, the expression of inflammatory mediators, growth factors, epithelial expression of melanocortin and sexual hormones receptors suggest that not only melanocytes, but entire epidermal melanin unit is involved in melasma physiopathology. Objectives To compare nuclear morphological features and chromatin texture between basal keratinocytes in facial melasma and adjacent normal skin. Methods We took facial skin biopsies (2 mm melasma and adjacent normal skin) from women processed for haematoxylin and eosin. Thirty non‐overlapping basal keratinocyte nuclei were segmented and descriptors of area, highest diameter, perimeter, circularity, pixel intensity, profilometric index (Ra) and fractal dimension were extracted using ImageJ software. Results Basal keratinocyte nuclei from facial melasma epidermis displayed larger size, irregular shape, hyperpigmentation and chromatin heterogeneity by fractal dimension than perilesional skin. Conclusion Basal keratinocytes from facial melasma display changes in nuclear form and chromatin texture, suggesting that the phenotype differences between melasma and adjacent facial skin can result from complete epidermal melanin unit alterations, not just hypertrophic melanocytes.