TY - JOUR
T1 - Purification and characterization of HSP-inducers from Eupatorium lindleyanum
AU - Yamashita, Yasuhiro
AU - Ikeda, Tsuyoshi
AU - Matsuda, Minoru
AU - Maji, Daisuke
AU - Hoshino, Tatsuya
AU - Mizushima, Tohru
N1 - Funding Information:
We thank Drs. Angelidis CE and Pagoulatos GN (University of Ioannina, Greece) and Dr. Nakai A (Yamaguchi University, Japan) for generously providing transgenic mice expressing HSP70 and antiserums and HSF1 expression vector, respectively. This work was supported by Grants-in-Aid for Scientific Research from the Ministry of Health, Labour, and Welfare of Japan , as well as the Japan Science and Technology Agency , Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan .
PY - 2012/4/1
Y1 - 2012/4/1
N2 - The expression of heat shock proteins (HSPs), particularly HSP70, provides resistance to stressors. We recently reported that ultraviolet (UV)-induced melanin production and skin damage were suppressed in transgenic mice expressing HSP70 and that an extract of Eupatorium lindleyanum induces the expression of HSP70 in cells. Here we report the purification of eupalinolide A and B (EA and EB) from E. lindleyanum, and describe their actions as HSP-inducers. EA and EB both induced the expression of HSP70 in cells at concentrations that did not significantly affect cell viability. Treatment of cells with EA or EB activated heat shock factor 1 (HSF1), while the artificial suppression of HSF1 expression diminished the EA- or EB-mediated induction of HSP70 expression. Furthermore, EB inhibited the interaction between HSF1 and HSP90, which is known to inhibit the activity of HSF1. These findings suggest that EA and EB induce the expression of HSP70 via the activation of HSF1 by inhibiting the interaction between HSF1 and HSP90. EA and EB both induced the expression of HSP70 synergistically with other stressors. Furthermore, pre-treatment of cells with EA or EB suppressed melanin production and stressor-induced apoptosis. These effects were suppressed by the artificial suppression of HSP70 expression. In vivo, the percutaneous administration of EB induced the expression of HSP70 and suppressed UVB radiation-induced damage, inflammatory responses and melanin production in the skin. These results suggest that EA and EB could be beneficial for use in cosmetics and medicines as a consequence of their inhibitory action on UV-induced skin damage and melanin production.
AB - The expression of heat shock proteins (HSPs), particularly HSP70, provides resistance to stressors. We recently reported that ultraviolet (UV)-induced melanin production and skin damage were suppressed in transgenic mice expressing HSP70 and that an extract of Eupatorium lindleyanum induces the expression of HSP70 in cells. Here we report the purification of eupalinolide A and B (EA and EB) from E. lindleyanum, and describe their actions as HSP-inducers. EA and EB both induced the expression of HSP70 in cells at concentrations that did not significantly affect cell viability. Treatment of cells with EA or EB activated heat shock factor 1 (HSF1), while the artificial suppression of HSF1 expression diminished the EA- or EB-mediated induction of HSP70 expression. Furthermore, EB inhibited the interaction between HSF1 and HSP90, which is known to inhibit the activity of HSF1. These findings suggest that EA and EB induce the expression of HSP70 via the activation of HSF1 by inhibiting the interaction between HSF1 and HSP90. EA and EB both induced the expression of HSP70 synergistically with other stressors. Furthermore, pre-treatment of cells with EA or EB suppressed melanin production and stressor-induced apoptosis. These effects were suppressed by the artificial suppression of HSP70 expression. In vivo, the percutaneous administration of EB induced the expression of HSP70 and suppressed UVB radiation-induced damage, inflammatory responses and melanin production in the skin. These results suggest that EA and EB could be beneficial for use in cosmetics and medicines as a consequence of their inhibitory action on UV-induced skin damage and melanin production.
KW - Cell death
KW - Eupalinolide
KW - Heat shock protein 70
KW - Melanogenesis
KW - Skin photoaging
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U2 - 10.1016/j.bcp.2011.12.040
DO - 10.1016/j.bcp.2011.12.040
M3 - Article
C2 - 22245466
AN - SCOPUS:84857365259
SN - 0006-2952
VL - 83
SP - 909
EP - 922
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 7
ER -