European Journal of Dermatology
MENUChanging expression of the genes related to human hair graying Volume 18, numéro 4, July-August 2008
Illustrations
Department of Anatomy, College of Medicine, Chungnam National University, 6 Moonwha-dong, Jung-gu, Daejeon 301-131, Korea, Department of Dermatology, School of Medicine, Gyeongsang National University, 90 Chilam-dong, Jinju 660-702, Korea
- Mots-clés : genes, hair graying, melanocytes, melanocyte stem cells, microphthalmia transcription factor
- DOI : 10.1684/ejd.2008.0434
- Page(s) : 397-9
- Année de parution : 2008
Hair graying is one of the prototypical signs of human aging, but its mechanism is largely unknown. To elucidate the mechanism of hair graying, we investigated gene expression related to melanogenesis in human hair. The key molecules in melanogenesis, microphthalmia-associated transcription factor-M (MITF-M), Sox10, Pax3, tyrosine related protein-1 (TRP-1), and tyrosinase, were absent or greatly reduced in the bulbs of white hair compared to black hair. Melanocyte stem cells (MSCs) or melanocytes express markers for neural crest cells, Sox10, Pax3, and MITF-M. Taken together, our data suggest that hair graying is caused by defective migration of MSCs into the bulb area of hair.