Epidermal growth factor receptor relocalization and kinase activity are necessary for directional migration of keratinocytes in DC electric fields

• Published in: Journal of cell science Vol. 112 ( Pt 12); no. 12; pp. 1967 - 1978
• Main Authors: Fang, K S, Ionides, E, Oster, G, Nuccitelli, R, Isseroff, R R
• Format: Journal Article
• Language: English
• Published: England 15-06-1999
• Subjects: Cell Movement - physiology; Electromagnetic Fields; Enzyme Inhibitors - pharmacology; ErbB Receptors - metabolism; Galvanic Skin Response; Humans; Keratinocytes - cytology; Phosphorylation; Protein-Tyrosine Kinases - antagonists & inhibitors; Reference Values; Signal Transduction - physiology
• ISSN: 0021-9533; 1477-9137
• DOI: 10.1242/jcs.112.12.1967

Human keratinocytes migrate towards the negative pole in DC electric fields of physiological strength. This directional migration is promoted by epidermal growth factor (EGF). To investigate how EGF and its receptor (EGFR) regulate this directionality, we first examined the effect of protein tyrosine kinase inhibitors, including PD158780, a specific inhibitor for EGFR, on this response. At low concentrations, PD158780 inhibited keratinocyte migration directionality, but not the rate of migration; at higher concentrations, it reduced the migration rate as well. The less specific inhibitors, genistein, lavendustin A and tyrphostin B46, reduced the migration rate, but did not affect migration directionality. These data suggest that inhibition of EGFR kinase activity alone reduces directed motility, and inhibition of multiple tyrosine kinases, including EGFR, reduces the cell migration rate. EGFR redistribution also correlates with directional migration. EGFR concentrated on the cathodal face of the cell as early as 5 minutes after exposure to electric fields. PD158780 abolished EGFR localization to the cathodal face. These data suggest that EGFR kinase activity and redistribution in the plasma membrane are required for the directional migration of keratinocytes in DC electric fields. This study provides the first insights into the mechanisms of directed cell migration in electric fields.