Downregulation of Dicer expression by serum withdrawal sensitizes human endothelial cells to apoptosis

被引:45
作者
Asada, Satoshi [1 ,2 ]
Takahashi, Tomosaburo [1 ,2 ]
Isodono, Koji [1 ,2 ]
Adachi, Atsuo [1 ,2 ]
Imoto, Hiroko [1 ,2 ]
Ogata, Takehiro [2 ]
Ueyama, Tomomi [2 ]
Matsubara, Hiroaki [1 ,2 ]
Oh, Hidemasa [2 ]
机构
[1] Kyoto Prefectural Univ Med, Dept Cardiovasc Med, Kyoto 6028566, Japan
[2] Kyoto Univ Hosp, Translat Res Ctr, Dept Expt Therapeut, Kyoto 606, Japan
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2008年 / 295卷 / 06期
关键词
caspase; 3; nitric oxide synthase 3;
D O I
10.1152/ajpheart.00233.2008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Downregulation of Dicer expression by serum withdrawal sensitizes human endothelial cells to apoptosis. Am J Physiol Heart Circ Physiol 295: H2512-H2521, 2008. First published October 31, 2008; doi:10.1152/ajpheart.00233.2008.-Although the modulated expression of Dicer is documented upon neoplastic transformation, little is known of the regulation of Dicer expression by environmental stimuli and its roles in the regulation of cellular functions in primary cells. In this study, we found that Dicer expression was downregulated upon serum withdrawal in human umbilical vein endothelial cells (HUVECs). Serum withdrawal induced a time-dependent repression of Dicer expression, which was specifically rescued by vascular endothelial cell growth factor or sphingosine-1-phosphate. When Dicer expression was silenced by short-hairpin RNA against Dicer, the cells were more prone to apoptosis under serum withdrawal, whereas the rate of apoptosis was comparable with control cells in the serum-containing condition. Real-time PCR-based gene expression profiling identified several genes, the expression of which was modulated by Dicer silencing, including adhesion and matrix-related molecules, caspase-3, and nitric oxide synthase 3 (NOS3). Dicer silencing markedly impaired migratory functions without affecting cell adhesion and repressed phosphorylation of focal adhesion kinase and proline-rich tyrosine kinase 2 in adherent HUVECs. Dicer knockdown upregulated caspase-3 and downregulated NOS3 expression, and serum withdrawal indeed increased caspase-3 and decreased NOS3 expression. Furthermore, the overexpression of Dicer in HUVECs resulted in a marked reduction in apoptosis upon serum withdrawal and a decreased caspase-3 and increased NOS3 expression. The inhibition of NOS activity by N-omega-nitro-L-arginine methyl ester abrogated the effect of Dicer overexpression to rescue the cells from serum withdrawal-induced apoptosis. These results indicated that serum withdrawal decreases Dicer expression, leading to an increased susceptibility to apoptosis through the regulation of caspase-3 and NOS3 expression.
引用
收藏
页码:H2512 / H2521
页数:10
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