x
Filter:
Filters applied
- Melanoma
- Bernerd, FrançoiseRemove Bernerd, Françoise filter
Melanoma
2 Results
- Original Article Melanocytes/MelanomaOpen Archive
Melanosome Distribution in Keratinocytes in Different Skin Types: Melanosome Clusters Are Not Degradative Organelles
Journal of Investigative DermatologyVol. 138Issue 3p647–656Published online: October 17, 2017- Ilse Hurbain
- Maryse Romao
- Peggy Sextius
- Emilie Bourreau
- Céline Marchal
- Françoise Bernerd
- and others
Cited in Scopus: 46The melanosome pattern was characterized systematically in keratinocytes in situ in highly, moderately, and lightly pigmented human skin, classified according to the individual typological angle, a colorimetric measure of skin color phenotype. Electron microscopy of skin samples showed qualitatively and quantitatively that in highly pigmented skin, although melanosomes are mostly isolated and distributed throughout the entire epidermis, clusters are also observed in the basal layer. In moderately and lightly pigmented skin, melanosomes are concentrated in the first layer of the epidermis, isolated—but for most of them, grouped as clusters of melanocores delimited by a single membrane. - Original Article Melanocytes/MelanomaOpen Access
Melanocytes Sense Blue Light and Regulate Pigmentation through Opsin-3
Journal of Investigative DermatologyVol. 138Issue 1p171–178Published online: August 22, 2017- Claire Regazzetti
- Laura Sormani
- Delphine Debayle
- Françoise Bernerd
- Meri K. Tulic
- Gian Marco De Donatis
- and others
Cited in Scopus: 174The shorter wavelengths of the visible light spectrum have been recently reported to induce a long-lasting hyperpigmentation but only in melano-competent individuals. Here, we provide evidence showing that OPN3 is the key sensor in melanocytes responsible for hyperpigmentation induced by the shorter wavelengths of visible light. The melanogenesis induced through OPN3 is calcium dependent and further activates CAMKII followed by CREB, extracellular signal-regulated kinase, and p38, leading to the phosphorylation of MITF and ultimately to the increase of the melanogenesis enzymes: tyrosinase and dopachrome tautomerase.