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首页> 外文期刊>Journal of biomedical science. >Down-regulation of human NDR gene in megakaryocytic differentiation of erythroleukemia K562 cells.
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Down-regulation of human NDR gene in megakaryocytic differentiation of erythroleukemia K562 cells.

机译:人类NDR基因在红白血病K562细胞巨核细胞分化中的下调。

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摘要

To study the control of hematopoietic cell differentiation, a human negative differentiation regulator (NDR) gene was identified by the comparative analysis of differentially expressed genes in hemato-lymphoid tissues. NDR is expressed preferentially in the adult bone marrow, fetal liver and testis. Immunocytochemistry with anti-NDR antiserum showed the presence of NDR in human erythroleukemia K562 cell line and CD34+ cells sorted from the umbilical cord blood. When fused to the green fluorescent protein (GFP), NDR was directed to the nucleus of mouse 3T3 and K562 cells. Fusion protein with a deletion from residues 7 to 87 was detected in the cytoplasm. NDR appeared not to affect the proliferation of K562 cells when overly expressed. However, its expression was down-regulated during megakaryocytic differentiation of K562 cells induced by 12-O-tetradecanoylphorbol-13-acetate (TPA). Down-regulation of NDR correlated well with up-regulation of megakaryocytic markers, CD41 and CD61. Overexpression of the nuclear NDR-GFP in K562 cells inhibited the expression of CD41 and CD61 in megakaryocytic differentiation. Treatment of K562 cells with GF-109203X (GFX), an antagonist of the protein kinase C (PKC), blocked NDR down-regulation, up-regulated expression of CD41/CD61 and TPA-induced megakaryocytic differentiation. These results suggest a novel function of nuclear NDR protein in regulating hematopoietic cell development.
机译:为了研究对造血细胞分化的控制,通过对血液-淋巴组织中差异表达基因的比较分析,确定了人类负分化调节因子(NDR)基因。 NDR在成年骨髓,胎儿肝脏和睾丸中优先表达。带有抗NDR抗血清的免疫细胞化学显示,在人类红白血病K562细胞系和从脐带血中分选出的CD34 +细胞中存在NDR。当与绿色荧光蛋白(GFP)融合时,NDR被定向到小鼠3T3和K562细胞的细胞核。在细胞质中检测到从残基7至87缺失的融合蛋白。当过度表达时,NDR似乎不影响K562细胞的增殖。然而,其表达在由12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导的K562细胞的巨核细胞分化期间被下调。 NDR的下调与巨核细胞标志物CD41和CD61的上调密切相关。 K562细胞中核NDR-GFP的过表达抑制了巨核细胞分化中CD41和CD61的表达。用蛋白激酶C(PKC)的拮抗剂GF-109203X(GFX)处理K562细胞,可阻止NDR下调,CD41 / CD61表达上调以及TPA诱导的巨核细胞分化。这些结果表明核NDR蛋白在调节造血细胞发育中的新功能。

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