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Publication : Fate and plasticity of the epidermis in response to congenital activation of BRAF.

First Author  Krishnaswami SR Year  2015
Journal  J Invest Dermatol Volume  135
Issue  2 Pages  481-9
PubMed ID  25202828 Mgi Jnum  J:218061
Mgi Id  MGI:5616499 Doi  10.1038/jid.2014.388
Citation  Krishnaswami SR, et al. (2015) Fate and Plasticity of the Epidermis in Response to Congenital Activation of BRAF. J Invest Dermatol 135(2):481-9
abstractText  Germline and somatic mutations in RAS and its downstream effectors are found in several congenital conditions affecting the skin. Here we demonstrate that activation of BRAF in the embryonic mouse ectoderm triggers both craniofacial and skin defects, including hyperproliferation, loss of spinous and granular keratinocyte differentiation, and cleft palate. RNA sequencing of the epidermis confirmed these findings but unexpectedly revealed evidence of continued epidermal maturation, expression of >80 % of epidermal differentiation complex genes, and formation of a hydrophobic barrier. Spinous and granular differentiation were restored by pharmacologic inhibition of MAPK/ERK kinase or BRAF. However, restoration of epidermal differentiation was non-cell autonomous and required dermal tissue to be present in tissue recombination studies. These studies indicate that early activation of the RAF signaling pathway in the ectoderm has effects on specific steps of epidermal differentiation, which may be amenable to treatment with currently available pharmacologic inhibitors.
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