Inhibition of c-Kit signaling by diosmetin isolated from Chrysanthemum morifolium

被引:36
作者
Lee, Seong Jin [1 ]
Jung, Tae-Hoon [1 ]
Kim, Hojeong [2 ]
Jeong, Daeyoung [1 ]
Choi, Gildon [1 ]
Park, Woo-Kyu [1 ]
Kong, Jae Yang [3 ]
Jin, Mu-Hyun [2 ]
Cho, Heeyeong [1 ]
机构
[1] Korea Res Inst Chem Technol, Drug Discovery Div, Pharmacol Res Grp, Taejon 305343, South Korea
[2] LG Household Healthcare Ltd, Cosmet Res Ctr, Taejon 305343, South Korea
[3] Keimyung Univ, Coll Pharm, Taegu 704701, South Korea
基金
新加坡国家研究基金会;
关键词
c-Kit; Flavonoid; Diosmetin; Depigmentation; Chrysanthemum morifolium; HUMAN-MELANOMA CELLS; TYROSINE KINASE; IMATINIB MESYLATE; SKIN; MELANOGENESIS; MELANOCYTES; DIFFERENTIATION; PROLIFERATION; QUERCETIN; LUTEOLIN;
D O I
10.1007/s12272-013-0158-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The interaction of stem cell factor (SCF) with its cognate receptor c-Kit is closely associated with the survival and maturation of melanocytes. To investigate novel depigmentation agents, we screened 2,000 plant extracts for c-Kit inhibitors to identify active small molecules by using time-resolved fluorescence enzyme assays. For the active extracts identified as inhibitors of c-Kit enzyme, we evaluated the effects of the active extracts and isolated flavonoids on c-Kit phosphorylation in MO7e/melanocytes. Anti-melanogenic activity was also examined in melanocytes and melanoderm model. The flavonoids such as diosmetin, apigenin, acacetin and luteolin isolated from Chrysanthemum morifolium were found to be active in inhibiting c-Kit both at enzyme and cellular levels. In addition, these flavonoids attenuated SCF-induced proliferation of human primary melanocytes without toxicity and suppressed ultraviolet (UV) B irradiation-mediated melanin synthesis significantly. Among the active flavonoids, diosmetin was found to inhibit SCF-induced melanogenesis in a human melanoderm model. These results strongly suggest that C. morifolium extract and diosmetin have potential to suppress SCF-/UVB-induced melanogenesis, and could be developed as anti-pigmentation agents.
引用
收藏
页码:175 / 185
页数:11
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