Melanoblasts (Mbs) are thought to be strictly regulated by cell–cell interactions with epidermal keratinocytes, although the precise molecular mechanism of the regulation has been elusive. Notch signaling, whose activation is mediated by cell–cell interactions, is implicated in a broad range of developmental processes. We demonstrate the vital role of Notch signaling in the maintenance of Mbs, as well as melanocyte stem cells (MSCs). Conditional ablation of Notch signaling in the melanocyte lineage leads to a severe defect in hair pigmentation, followed by intensive hair graying. The defect is caused by a dramatic elimination of Mbs and MSCs. Furthermore, targeted overexpression of Hes1 is sufficient to protect Mbs from the elimination by apoptosis. Thus, these data provide evidence that Notch signaling, acting through Hes1, plays a crucial role in the survival of immature Mbs by preventing initiation of apoptosis.
Notch signaling via Hes1 transcription factor maintains survival of melanoblasts and melanocyte stem cells
Abbreviations used in this paper: d2EGFP, destabilized EGFP; DAPT, (3,5-difluorophenylacetyl)-l-alanyl-l-2-phenylglycine t-butyl ester; Dct, dopachrome tautomerase; E, embryonic day; HF, hair follicle; HM, hair matrix; LPP, lower permanent portion; Mb, melanoblast; MC, melanocyte; MSC, melanocyte stem cell; NICD, Notch intracellular domain; P, postnatal day; Q-PCR, quantitative PCR; Tg, transgenic; Tyr, tyrosinase.
Mariko Moriyama, Masatake Osawa, Siu-Shan Mak, Toshiyuki Ohtsuka, Norio Yamamoto, Hua Han, Véronique Delmas, Ryoichiro Kageyama, Friedrich Beermann, Lionel Larue, Shin-Ichi Nishikawa; Notch signaling via Hes1 transcription factor maintains survival of melanoblasts and melanocyte stem cells . J Cell Biol 8 May 2006; 173 (3): 333–339. doi: https://doi.org/10.1083/jcb.200509084
Download citation file:
Sign in
Client Account
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement