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Fascin 1 is transiently expressed in mouse melanoblasts during development and promotes migration and proliferation
Author(s) -
Yafeng Ma,
Ang Li,
William J. Faller,
Silvana Libertini,
Florencia Fiorito,
David A. Gillespie,
Owen J. Sansom,
Shigeko Yamashiro,
Laura M. Machesky
Publication year - 2013
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.089789
Subject(s) - fascin , biology , microbiology and biotechnology , melanocyte , cell migration , pseudopodia , lamellipodium , cell growth , cell cycle , cell , melanoma , cancer research , actin , genetics
Fascins, a family of actin-bundling proteins, are expressed in a spatially and temporally restricted manner during development and often in cancer. Fascin 1 has a clear role in cell migration in vitro, but its role in vivo in mammals is not well understood. Here, we investigate the role of fascin 1 in the melanocyte lineage and in melanoma cells. Fascin 1 knockout causes hypopigmentation in adult mice owing to migration and cell cycle progression defects in melanoblasts, the melanocyte precursor cell. Study of live embryo skin explants reveals that E14.5 fascin 1-null melanoblasts migrate slower, and generate fewer and thinner pseudopods. By contrast, fascin 1 expression drives faster migration and lamellipodia protrusion in melanocytes in vitro. In addition, fascin 1 depletion retards melanoblast proliferation in vivo and melanoma cell growth in vitro. These data indicate that fascin 1 not only promotes cell migration in mouse melanocytes but it also has a role in growth and cell cycle progression.

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