The suppression of zfpm-1 accelerates the erythropoietic differentiation of human CD34+ cells

被引:8
作者
Yang, Hee-Young
Kim, Sue Hee
Kim, Seok-Ho
Kim, Dong-Jun
Kim, Sun-Uk
Yu, Dae-Yeul
Il Yeom, Young
Lee, Dong-Seok
Kim, Yong-Jun
Park, Byung-Ju
Lee, Tae-Hoon
机构
[1] Chonnam Natl Univ, Sch Dent, Dent Sci Res Inst, Dept Oral Biochem, Kwangju 500757, South Korea
[2] Kangwon Natl Univ, Dept Anim Biotechnol, Chunchon, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Lab Human Genom, Taejon, South Korea
[4] Chonbuk Natl Univ, Coll Vet Med, Lab Obstet, Jeonju, South Korea
[5] Chonnam Natl Univ, Dept Mol Med, Kwangju, South Korea
基金
新加坡国家研究基金会;
关键词
hematopoietic stem cell; erythropoiesis; Zfpm-1; GATA-1; c-myc; c-myb; Zfpm-2;
D O I
10.1016/j.bbrc.2006.12.155
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
Erythropoiesis is a complex multistage process for the differentiation of mature erythrocytes from hematopoictic stem cells. The function of several transcription factors has been reported in hernatopoictic stem cell differentiation. However, the molecular basis governing its functional behavior is unclear. In this study, we characterized the role of Zfpm-1 during the erythropoietic differentiation of human hernatopoietic stem cells. To verify the function of 4fpm-1 during erythropoietic differentiation, we established human CD34(+) cell culture system by using human umbilical cord blood. At day 7 of the human CD34(+) cell differentiation process to proerythocytes, Zfpm-1 was initially up-regulated and then dramatically down-regulated at day 9. The Zfpm-1 siRNA transfected HSCs contained 20% more GPA(+) cells than the mock transfected cells, and showed repressed expression of the hernatopoietic transcription factors, c-myc and c-myb, but increased expression of GATA-1. In contrast, the Zfpm-1 gain-of-function is the opposite of loss-of-function results above. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:978 / 984
页数:7
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