Differential expression changes in K562 cells during the hemin-induced erythroid differentiation and the phorbol myristate acetate (PMA)-induced megakaryocytic differentiation

被引:32
作者
Huo, Xiao-Fang [1 ]
Yu, Jia [1 ]
Peng, Han [1 ]
Du, Zhan-Wen [1 ]
Liu, Xiao-Ling [1 ]
Ma, Yan-Ni [1 ]
Zhang, Xin [1 ]
Zhang, Yao [1 ]
Zhao, Hua-Lu [1 ]
Zhang, Jun-Wu [1 ]
机构
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Natl Lab Med Mol Biol, Beijing 100005, Peoples R China
基金
中国国家自然科学基金;
关键词
K562; cells; erythroid differentiation; megakaryocytic differentiation; DDRT-PCR; signaling pathways;
D O I
10.1007/s11010-006-9229-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
K562 cell line has been used as a model of common progenitor of erythroblasts and magakaryocytes and can be differentiated into erythroid and megakaryocytic lineages by hemin and phorbol myristate acetate (PMA) respectively. We analyzed mRNA expression in un-induced, hemin-induced and PMA-induced K562 cells by differential display reverse transcription polymerase chain reaction (DDRT-PCR) method. 314 differential expression sequence tags (ESTs) were obtained. Among them, 201 ESTs displayed up-regulation and 85 ESTs down-regulation after hemin induction, 186 ESTs showed up-regulation and 72 ESTs down-regulation after PMA induction. The differentially expressed genes included those encoding transcription factors, signaling factors, apoptosis-associated factors and others. 45 of these ESTs stand for genes whose open reading frames were found but whose functions remain unknown. 4 ESTs represent possibly new genes. Furthermore we compared differences of gene expression during hemin-induced erythroid differentiation and PMA-induced megakaryocytic differentiation and found that the expressional changes of some transcription factors and metabolism proteins are the common but the expressional changes of some signal pathways in these two differentiation processes are different. These results suggested that erythroid differentiation and megakaryocytic differentiation are associated in activation and repression of different signal pathways.
引用
收藏
页码:155 / 167
页数:13
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