基因沉默
转染
RNA干扰
小干扰RNA
癌症研究
分子生物学
骨髓
生物
造血
信使核糖核酸
细胞凋亡
基因表达
外周血单个核细胞
髓样
基因敲除
细胞培养
细胞生长
白细胞介素3
下调和上调
基因表达调控
细胞
细胞周期
Jurkat细胞
核糖核酸
骨髓增生异常综合症
小发夹RNA
K562细胞
细胞生物学
HEK 293细胞
作者
Zonghong Shao,Wei Zhang,Rong Fu,Lijuan Li,Huaquan Wang
出处
期刊:Blood
[Elsevier BV]
日期:2012-11-16
卷期号:120 (21): 4934-4934
被引量:1
标识
DOI:10.1182/blood.v120.21.4934.4934
摘要
Abstract Abstract 4934 Objective To investigate the expression of TET2 mRNA in bone marrow mononuclear cells(BMMNC), CD3+ T cells and CD34+ cells of patients with myelodysplastic syndrome(MDS)and to study the effect of silencing TET2 by Small interfering RNA (siRNA) on the biological characteristics of CD34+ cells. Methods CD3+ T cells and CD34+ cells were sorted by magnetic activated cell-sorting system. The expression of TET2 mRNA was detected by qPCR. The silencing effect of RNA interference (RNAi) on TET2 expression was identified by qPCR and Western blot analysis. The cell cycle kinetics and cell apoptosis were detected by flowcytometry. Results The expressions of TET2 mRNA in BMMNC, CD3+ T cells and CD34+ cells were down-regulated in MDS compared with that in controls. The siRNA targeting TET2 suppressed the expression of TET2 in CD34+ cells. Meanwhile, the proliferation activity was significantly enhanced and the apoptosis rate was declined in cells which transfected with TET2 siRNA as compared to those of the cells transfected with scrambled siRNA and control cells. Conclusions The mRNA expressions of TET2 in BMMNC, CD3+ T cells and CD34+ cells of MDS patients were decreased. Suppression of TET2 expression renders the CD34+ cells harboring more aggressive phenotype. This preliminary finding suggests that CD34+ cells lowering expression of TET2 may play an oncogenic role on myeloid tumor. Disclosures: No relevant conflicts of interest to declare.
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