TY - JOUR
T1 - Quantification of inducible SOS-like photoprotective responses in human skin
AU - Arad, Simin
AU - Konnikov, Nellie
AU - Goukassian, David A.
AU - Gilchrest, Barbara A.
N1 - Funding Information:
We are grateful to Dr Gregory Galico and Dr Thomas Cochran, who in addition to N.K. provided adult skin for organ cultures; to Daniella Adrien for assistance in the preparation of the paper. This work was supported by grants from the Herzog Foundation and NIH-RO-1 CA 10515 (to B.A.G.).
PY - 2007/11
Y1 - 2007/11
N2 - To document and quantify inducible photoprotective effects in human skin, explant cultures were treated once with thymidine dinucleotide (pTT) or diluent alone or UV-irradiated. Both pTT and UV increased the melanogenic protein levels on days 1-5 and comparably increased melanocyte dendricity and epidermal melanin content. Explants treated with pTT or UV but not with diluent alone showed initial inhibition of epidermal proliferation followed by mild reactive hyperplasia; melanocyte proliferation was minimal. To determine whether pTT and UV provide comparable protection against subsequent UV-induced DNA damage, explants were pTT- or diluent-treated or UV-irradiated. All explants were then irradiated with the same UV dose 72 hours later. Compared to diluent alone, pTT or UV pretreatment decreased the number of epidermal cells positive for cyclobutane pyrimidine dimers (CPDs) 50% immediately post-irradiation. In pTT- and UV- versus diluent-pretreated explants, the rate of CPD removal was also more rapid, approximately 80 vs 45% of the initial burden within 72 hours. These data confirm and quantify comparable SOS-like responses in human skin after pTT or UV irradiation, attributable to both increased epidermal melanin and increased DNA repair rate, in the case of pTT in the absence of initial damage.
AB - To document and quantify inducible photoprotective effects in human skin, explant cultures were treated once with thymidine dinucleotide (pTT) or diluent alone or UV-irradiated. Both pTT and UV increased the melanogenic protein levels on days 1-5 and comparably increased melanocyte dendricity and epidermal melanin content. Explants treated with pTT or UV but not with diluent alone showed initial inhibition of epidermal proliferation followed by mild reactive hyperplasia; melanocyte proliferation was minimal. To determine whether pTT and UV provide comparable protection against subsequent UV-induced DNA damage, explants were pTT- or diluent-treated or UV-irradiated. All explants were then irradiated with the same UV dose 72 hours later. Compared to diluent alone, pTT or UV pretreatment decreased the number of epidermal cells positive for cyclobutane pyrimidine dimers (CPDs) 50% immediately post-irradiation. In pTT- and UV- versus diluent-pretreated explants, the rate of CPD removal was also more rapid, approximately 80 vs 45% of the initial burden within 72 hours. These data confirm and quantify comparable SOS-like responses in human skin after pTT or UV irradiation, attributable to both increased epidermal melanin and increased DNA repair rate, in the case of pTT in the absence of initial damage.
UR - https://www.scopus.com/pages/publications/35348918798
U2 - 10.1038/sj.jid.5700893
DO - 10.1038/sj.jid.5700893
M3 - Article
C2 - 17522706
AN - SCOPUS:35348918798
SN - 0022-202X
VL - 127
SP - 2629
EP - 2636
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 11
ER -