Ma, Y., Li, A., Faller, W.J., Libertini, S., Fiorito, F., Gillespie, D.A., Sansom, O.J. , Yamashiro, S. and Machesky, L.M. (2013) Fascin 1 is transiently expressed in mouse melanoblasts during development and promotes migration and proliferation. Development, 140(10), pp. 2203-2211. (doi: 10.1242/dev.089789)
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Abstract
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.
Item Type: | Articles |
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Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | Libertini, Dr Silvana and Li, Mr Ang and Gillespie, Professor David and Machesky, Professor Laura and Faller, Dr William and Ma, Dr Yafeng and Sansom, Professor Owen |
Authors: | Ma, Y., Li, A., Faller, W.J., Libertini, S., Fiorito, F., Gillespie, D.A., Sansom, O.J., Yamashiro, S., and Machesky, L.M. |
College/School: | College of Medical Veterinary and Life Sciences > School of Cancer Sciences |
Journal Name: | Development |
Publisher: | The Company of Biologists Ltd |
ISSN: | 0950-1991 |
Copyright Holders: | Copyright © 2013 The Company of Biologists Ltd |
First Published: | First published in Development 140(10):2203-2211 |
Publisher Policy: | Reproduced under a Creative Commons License |
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