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Ultraviolet light induces Stat3 activation in human keratinocytes and fibroblasts through reactive oxygen species and DNA damage
Author(s) -
Bito Toshinori,
Sumita Naoko,
Masaki Taro,
Shirakawa Toshiro,
Ueda Masato,
Yoshiki Ryutaro,
Tokura Yoshiki,
Nishigori Chikako
Publication year - 2010
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2010.01084.x
Subject(s) - dna damage , xeroderma pigmentosum , reactive oxygen species , human skin , transfection , microbiology and biotechnology , dna repair , dna , chemistry , ultraviolet light , keratinocyte , biology , in vitro , gene , photochemistry , biochemistry , genetics
Please cite this paper as: Ultraviolet light induces Stat3 activation in human keratinocytes and fibroblasts through reactive oxygen species and DNA damage. Experimental Dermatology 2010; 19: 654–660. Abstract: Stat3 is activated by the outer stressors, such as ultraviolet (UV) exposure. In this study, we investigated the Stat3 response to UV irradiation in human epidermal keratinocytes and dermal fibroblasts. Results indicated that UVB and UVC differentially activate Stat3 in these cells. The UV‐induced Stat3 activation was mediated by both reactive oxygen species (ROS) and DNA damage, and the dominancy of ROS and DNA damage to activate Stat3 depended on the wavelength of UV. By using fibroblasts from a patient with xeroderma pigmentosum A (XP‐A) and those transfected with human XPA gene, we found that UVB activates Stat3 via both ROS and DNA damage, while UVC does so mainly via DNA damage. The present data suggest that Stat3 activation in UV‐exposed human skin is one of the initial events where DNA damage and ROS are involved.