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Fig. 7. HOXA3 promotes keratinocyte migration in a uPAR-dependent manner. Photomicrographs of BALB/c MK keratinocytes stably transfected with control cDNA (original magnification x40) (a) or HOXA3 construct (b), 48 hours after administration of a scratch wound (denuded area indicated with black box outline). (c) Quantitative analysis of migration following scratch wounds in control or HOXA3-expressing keratinocytes in the presence or absence of function-blocking antibodies against murine uPAR. Results are the means±s.d. of 12 experiments.





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