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Mol Cell Biochem. 2006 Mar;284(1-2):183-8. Epub 2006 Jan 13.

Decreased keratinocyte motility in skin wound on mice lacking the epidermal fatty acid binding protein gene.

Author information

1
Department of Dermatology, Tohoku University Graduate School of Medicine, Tohoku, Japan.

Erratum in

  • Mol Cell Biochem. 2007 May;299(1-2):1-3.

Abstract

Fatty acids are shown to be important in various skin functions. Fatty acid binding protein (FABP) is postulated to serve as a lipid shuttle, solubilizing hydrophobic fatty acids and delivering them to the appropriate metabolic system. Among the FABP family proteins, epidermal-type FABP (E-FABP) is solely expressed in keratinocyte but its specific role in skin is not yet fully established. We found an elevated expression of E-FABP in regenerative keratinocytes of healing wounds. However, E-FABP null mice showed no marked differences compared to wild type mice in the process of wound closure, in vivo. On the other hand, in keratinocyte culture, E-FABP gene disruption decreased the cell motility, but did not affect the cell proliferation. E-FABP deletion may be compensated for in vivo by the microenvironment comprised of various cells such as fibroblasts and endothelial cells around the wound. Our analyses suggest that the E-FABP elevation may be necessary for the activation of cell motility within regenerative epidermis during wound healing.

PMID:
16411018
DOI:
10.1007/s11010-005-9048-8
[Indexed for MEDLINE]

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