Welcome to the Wikiversity learning project for human skin pigmentation. Participants explore melanin, melanosomes, melanocytes, MSH and its receptors and the control of skin pigmentation.
This learning project is initially organized around suggested reading and discussion. Feel free to add new reading and subsections for questions and discussion.
Working with mice, the transcription factor Foxn1 and the growth factor FGF2 were found to be involved in the melanocyte-keratinocyte interactions that allow melanosomes to be distributed in the skin[1]. Foxn1 was originally studied because of its importance in the development of the thymus as revealed by Foxn1 mutant nude mice. Foxn1 mutations also cause failure of human hair growth[2].
↑"Dedicated epithelial recipient cells determine pigmentation patterns" by L. Weiner, R. Han, B. M. Scicchitano, J. Li, K. Hasegawa, M. Grossi, D. Lee and J. L Brissette in Cell (2007) Volume 130, pages 932-942.Entrez PubMed17803914
↑"Exposing the human nude phenotype" by J. Frank, C. Pignata, A.A. Panteleyev, D. M. Prowse, H. Baden, L. Weiner, L. Gaetaniello, W. Ahmad, N. Pozzi, P. B. Cserhalmi-Friedman, V. M. Aita, H. Uyttendaele, D. Gordon, J. Ott, J. L. Brissette and A. M. Christiano in Nature (1999) Volume 398, pages 473-474. Entrez PubMed15316080