TLR4 expression in mouse embryonic stem cells and in stem cell-derived vascular cells is regulated by epigenetic modifications

被引:53
|
作者
Zampetaki, Anna [1 ]
Xiao, Qingzhong [1 ]
Zeng, Lingfang [1 ]
Hu, Yanhua [1 ]
Xu, Qingbo [1 ]
机构
[1] St Georges Univ, Dept Cardiac & Vasc Sci, London SW17 0RE, England
关键词
endotoxin challenge; DNA methylation; histone hypoacetylation;
D O I
10.1016/j.bbrc.2006.06.055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Embryonic stem (ES) cells and ES cell-derived differentiated cells can be used in tissue regeneration approaches. However, inflammation may pose a major hurdle. To define the inflammatory response of ES and ES cell-derived vascular cells, we exposed these cells to LPS. With the exception of MIF no significant cytokine mRNA levels were observed either at baseline or after stimulation. Further experiments revealed that these cells do not express TLR4. Analysis of the DNA methylation status of the TLR4 upstream region showed increased methylation. Moreover, in vitro methylation suppressed TLR4 promoter activity in reporter gene assays. ChIP assays showed that in this region histories H3 and H4 are hypoacetylated in ES cells. Interestingly, 5-aza-dC or TSA partially relieves this gene repression. Finally, the increased levels of TLR4 observed in ES cells after treatment with 5-aza-dC or TSA confer responsiveness to LPS, as induction of IL-6 and TNF alpha mRNA was detected in endotoxin stimulated ES cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 99
页数:11
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