Abstract
Previously, we reported that fetuin-A is a major component of ovine foetal skin and significantly enhances 'wound closure' in primary keratinocyte cultures. In this study, we found that in human newborn foreskin, a high level of fetuin-A protein is detected throughout the dermis. However, in adult skin a low level of fetuin-A is observed throughout the epidermal and dermal layers, except at regions surrounding hair follicles and at the epidermal-dermal junction where the level of fetuin-A is relatively high. Fetuin-A significantly induces actin-rich protrusions in human primary keratinocytes. Interestingly, blockade of epidermal growth factor (EGF) receptor signalling has a limited effect on fetuin-A promoted 'wound closure' on primary human keratinocytes, but significantly inhibits fetuin-A's effect on HaCaT cells. These results indicate that high levels of fetuin-A may partially contribute to less scar formation in newborn foreskin and that the effect of fetuin-A on primary keratinocyte migration is independent of EGF receptor signalling. © 2009 John Wiley & Sons A/S.
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Wang, X. Q., Hung, B. S., Kempf, M., Liu, P. Y., Dalley, A. J., Saunders, N. A., & Kimble, R. M. (2010, August). Fetuin-A promotes primary keratinocyte migration: Independent of epidermal growth factor receptor signalling. Experimental Dermatology. https://doi.org/10.1111/j.1600-0625.2009.00978.x
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