Low power millimeter wave irradiation exerts no harmful effect on human keratinocytes in vitro

• Published in: Bioelectromagnetics 2003-04, Vol.24 (3), p.165-173
• Main Authors: Szabo, Imre, Manning, Michael R., Radzievsky, Alexander A., Wetzel, Michele A., Rogers, Thomas J., Ziskin, Marvin C.
• Format: Article
• Language: English
• Subjects: Cell Communication - radiation effects; Cell Survival - radiation effects; Cells, Cultured; chemokine; Chemokine CCL5 - analysis; Chemokine CCL5 - biosynthesis; Chemokine CXCL10; Chemokines, CXC - analysis; Chemokines, CXC - biosynthesis; Dose-Response Relationship, Radiation; gap junctional communication; HaCaT; heat shock protein; Heat-Shock Proteins - analysis; Heat-Shock Proteins - biosynthesis; Humans; Intercellular Junctions - radiation effects; Intercellular Junctions - ultrastructure; Keratinocytes - cytology; Keratinocytes - metabolism; Keratinocytes - radiation effects; Microwaves - adverse effects; Radiation Dosage; Reference Values; vital staining
• ISSN: 0197-8462; 1521-186X
• DOI: 10.1002/bem.10077

Low power millimeter wave (LP‐MW) irradiation has been successfully used in clinical practice as an independent and/or supplemental therapy in patients with various diseases. It is still not clear, however, whether exposed skin is directly affected by repeated LP‐MW irradiation and whether cells of the epidermis can be activated by the absorbed energy. Keratinocytes, the most numerous component of the epidermis are believed to manifest functional responses to physical stimuli. In this study we analyzed whether LP‐MW irradiation modulated the production of chemokines, including RANTES and IP‐10 of keratinocytes in vitro. We also investigated whether LP‐MW irradiation induces a heat stress reaction in keratinocytes, and stimulates heat shock protein 70 (Hsp70) production. Vital staining of keratinocytes with carboxyfluorescein succinimidyl ester and ethidium bromide was used to analyze the MW effect on the viability of adherent cells. In addition, we studied the effect of LP‐MW irradiation on intercellular gap junctional communication in keratinocyte monolayers by Lucifer yellow dye transfer. We found no significant changes in constitutive RANTES and inducible IP‐10 production following LP‐MW irradiation. LP‐MW exposure of keratinocyte monolayers did not alter Hsp70 production, unlike exposure to higher power MWs (HP‐MW) or hyperthermia (43 °C; 1 h). LP‐MW irradiation and hyperthermia did not alter the viability of adherent keratinocytes, while HP‐MW irradiation induced cellular damage within the beam area. Finally, we found no alteration in the gap junctional intercellular communication of keratinocytes following LP‐MW irradiation, which on the other hand, was significantly increased by hyperthermia. In summary, we detected no harmful effect of LP‐MW irradiation on both keratinocyte function and structure in vitro, although these cells were sensitive to higher MW power that developed heat stress reaction and cellular damage. Our results provide further evidence that LP‐MW irradiation does not induce evidence of skin inflammation or keratinocyte damage and that its clinical application appears to be safe. Bioelectromagnetics 24:165–173, 2003. © 2003 Wiley‐Liss, Inc.