C-Kit Binding Properties of Hesperidin (a Major Component of KMP6) as a Potential Anti-Allergic Agent

被引:10
作者
Jeong, Hyun-Ja [1 ]
Choi, Youngjin [1 ]
Kim, Kyu-Yeob [2 ]
Kim, Min-Ho [3 ]
Kim, Hyung-Min [2 ]
机构
[1] Hoseo Univ, Biochip Res Ctr, Asan, South Korea
[2] Kyung Hee Univ, Dept Pharmacol, Seoul, South Korea
[3] Chonbuk Natl Univ, High Enthalpy Plasma Res Ctr, Jeonju, South Korea
关键词
STEM-CELL FACTOR; FACTOR-INDUCED MIGRATION; MAST-CELLS; TNF-ALPHA; ACTIVATION; EXPRESSION; DIFFERENTIATION; INFLAMMATION; PATHWAYS; RECEPTOR;
D O I
10.1371/journal.pone.0019528
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Accumulation of mast cells can be causally related to several allergic inflammations. Stem cell factor (SCF) as a mast cell chemotaxin induces mast cell migration. To clarify a new effect of Pyeongwee-San extract (KMP6, a drug for indigestion) for the treatment of allergy, we investigated the effects of KMP6 on SCF-induced migration of rat peritoneal mast cells (RPMCs). A molecular docking simulation showed that hesperidin, a major component of KMP6, controls the SCF and c-kit binding by interaction with the active site of the c-kit. KMP6 and hesperidin significantly inhibited SCF-induced migration of RPMCs (P<0.05). The ability of the SCF to enhance morphological alteration and F-actin formation was also abolished by treatment with KMP6 or hesperidin. KMP6 and hesperidin inhibited SCF-induced p38 MAPK activation. In addition, SCF-induced inflammatory cytokine production was significantly inhibited by treatment with KMP6 or hesperidin (P<0.05). Our results show for the first time that KMP6 potently regulates SCF-induced migration, p38 MAPK activation and inflammatory cytokines production through hindrance of SCF and c-kit binding in RPMCs. Such modulation may have functional consequences during KMP6 treatment, especially mast cell-mediated allergic inflammation disorders.
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页数:8
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