Role of canonical Wnt signaling/β-catenin viaDermo1in cranial dermal cell development
Author(s) -
Thu Hương Trần,
Andrew Jarrell,
Gabriel E. Zentner,
Adrienne L Welsh,
Isaac Brownell,
Peter C. Scacheri,
Radhika P. Atit
Publication year - 2010
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.754
H-Index - 325
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.056473
Subject(s) - wnt signaling pathway , biology , neural crest , cranial neural crest , ectoderm , microbiology and biotechnology , progenitor cell , mesoderm , cell fate determination , zebrafish , anatomy , beta catenin , population , stem cell , transcription factor , genetics , signal transduction , embryonic stem cell , embryogenesis , embryo , gene , sociology , demography
Cranial dermis develops from cephalic mesoderm and neural crest cells, but what signal(s) specifies the dermal lineage is unclear. Using genetic tools to fate map and manipulate a cranial mesenchymal progenitor population in the supraorbital region, we show that the dermal progenitor cells beneath the surface ectoderm process canonical Wnt signaling at the time of specification. We show that Wnt signaling/β-catenin is absolutely required and sufficient for Dermo1 expression and dermal cell identity in the cranium. The absence of the Wnt signaling cue leads to formation of cartilage in craniofacial and ventral trunk regions at the expense of dermal and bone lineages. Dermo1 can be a direct transcription target and may mediate the functional role of Wnt signaling in dermal precursors. This study reveals a lineage-specific role of canonical Wnt signaling/β-catenin in promoting dermal cell fate in distinct precursor populations.
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