Arctiin blocks hydrogen peroxide-induced senescence and cell death though microRNA expression changes in human dermal papilla cells

被引:30
作者
Bae, Seunghee [1 ]
Lim, Kyung Mi [1 ]
Cha, Hwa Jun [1 ]
An, In-Sook [1 ]
Lee, Jeong Pyo [2 ]
Lee, Kwang Sik [2 ]
Lee, Ghang Tai [2 ]
Lee, Kun Kook [2 ]
Jung, Ho Jung [3 ]
Ahn, Kyu Joong [3 ]
An, Sungkwan [1 ]
机构
[1] Konkuk Univ, Korea Inst Skin & Clin Sci, Seoul 143701, South Korea
[2] Coreana Cosmet Co Ltd, Cheonan Si 330833, Chungcheongnam, South Korea
[3] Konkuk Univ, Dept Dermatol, Sch Med, Seoul 143701, South Korea
关键词
Dermal papilla cell; Senescence; Cell death; microRNA; Arctiin; HUMAN HAIR FOLLICLE; OXIDATIVE STRESS; ANDROGENETIC ALOPECIA; HACAT KERATINOCYTES; INDUCED DAMAGE; APOPTOSIS; PROLIFERATION; GROWTH; FIBROBLASTS; INHIBITION;
D O I
10.1186/0717-6287-47-50
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Accumulating evidence indicates that reactive oxygen species (ROS) are an important etiological factor for the induction of dermal papilla cell senescence and hair loss, which is also known alopecia. Arctiin is an active lignin isolated from Arctium lappa and has anti-inflammation, anti-microbial, and anti-carcinogenic effects. In the present study, we found that arctiin exerts anti-oxidative effects on human hair dermal papilla cells (HHDPCs). Results: To better understand the mechanism, we analyzed the level of hydrogen peroxide (H2O2)-induced cytotoxicity, cell death, ROS production and senescence after arctiin pretreatment of HHDPCs. The results showed that arctiin pretreatment significantly inhibited the H2O2-induced reduction in cell viability. Moreover, H2O2-induced sub-G1 phase accumulation and G2 cell cycle arrest were also downregulated by arctiin pretreatment. Interestingly, the increase in intracellular ROS mediated by H2O2 was drastically decreased in HHDPCs cultured in the presence of arctiin. This effect was confirmed by senescence associated-beta galactosidase (SA-beta-gal) assay results; we found that arctiin pretreatment impaired H2O2-induced senescence in HHDPCs. Using microRNA (miRNA) microarray and bioinformatic analysis, we showed that this anti-oxidative effect of arctiin in HHDPCs was related with mitogen-activated protein kinase (MAPK) and Wnt signaling pathways. Conclusions: Taken together, our data suggest that arctiin has a protective effect on ROS-induced cell dysfunction in HHDPCs and may therefore be useful for alopecia prevention and treatment strategies.
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页数:11
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