PI3K and ERK signaling pathways are involved in differentiation of monocytic cells induced by 27-hydroxycholesterol

被引:9
|
作者
Son, Yonghae [1 ,5 ]
Kim, Bo-Young [1 ]
Park, Young Chul [2 ]
Eo, Seong-Kug [3 ,4 ]
Chos, Hyok-rae [6 ]
Kim, Koanhoi [1 ]
机构
[1] Pusan Natl Univ, Sch Med, Dept Pharmacol, Yangsan 50612, South Korea
[2] Pusan Natl Univ, Sch Med, Dept Microbiol & Immunol, Yangsan 50612, South Korea
[3] Chonbuk Natl Univ, Coll Vet Med, Iksan 54596, South Korea
[4] Chonbuk Natl Univ, Biosafety Res Inst, Iksan 54596, South Korea
[5] Pusan Natl Univ, Inst Marine Biotechnol, Busan 46241, South Korea
[6] Kosin Univ, Coll Med, Dept Neurosurg, Busan 49267, South Korea
来源
基金
新加坡国家研究基金会;
关键词
Dendritic cells; Differentiation; ERK; PI3K; 27-hydroxycholesterol; DENDRITIC CELLS; ATHEROSCLEROSIS; INFLAMMATION; LYMPHOCYTES; OXYSTEROLS; MECHANISMS; EXPRESSION; MIGRATION; CANCER; CCL2;
D O I
10.4196/kjpp.2017.21.3.301
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
27-Hydroxycholesterol induces differentiation of monocytic cells into mature dendritic cells, mDCs. In the current study we sought to determine roles of the PI3K and the ERK pathways in the 27OHChol-induced differentiation. Up-regulation of mDC-specific markers like CD80, CD83 and CD88 induced by stimulation with 27OHChol was significantly reduced in the presence of LY294002, an inhibitor of PI3K, and U0126, an inhibitor of ERK. Surface expression of MHC class I and II molecules elevated by 27OHChol was decreased to basal levels in the presence of the inhibitors. Treatment with LY294002 or U0126 resulted in recovery of endocytic activity which was reduced by 27OHChol. CD197 expression and cell adherence enhanced by 27OHChol were attenuated in the presence of the inhibitors. Transcription and surface expression of CD molecules involved in atherosclerosis such as.CD105, CD137 and CD166 were also significantly decreased by treatment with LY294002 and U0126. These results mean that the PI3K and the ERK signaling pathways are necessary for differentiation of monocytic cells into mDCs and involved in over-expression of atherosclerosis-associated molecules in response to 27OHChol.
引用
收藏
页码:301 / 308
页数:8
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