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抑制zfpm-1可加速人CD34+细胞的红细胞生成分化。

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

作者信息

Yang Hee-Young, Kim Sue Hee, Kim Seok-Ho, Kim Dong-Jun, Kim Sun-Uk, Yu Dae-Yeul, Yeom Young Il, Lee Dong-Seok, Kim Yong-Jun, Park Byung-Ju, Lee Tae-Hoon

机构信息

Department of Molecular Medicine, Chonnam National University, Gwangju, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2007 Feb 23;353(4):978-84. doi: 10.1016/j.bbrc.2006.12.155. Epub 2006 Dec 28.

Abstract

Erythropoiesis is a complex multistage process for the differentiation of mature erythrocytes from hematopoietic stem cells. The function of several transcription factors has been reported in hematopoietic 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 hematopoietic stem cells. To verify the function of Zfpm-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 hematopoietic 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.

摘要

红细胞生成是一个复杂的多阶段过程,涉及造血干细胞分化为成熟红细胞。已有报道称几种转录因子在造血干细胞分化中发挥作用。然而,其功能行为的分子基础尚不清楚。在本研究中,我们对Zfpm-1在人类造血干细胞红细胞生成分化过程中的作用进行了表征。为了验证Zfpm-1在红细胞生成分化过程中的功能,我们利用人脐带血建立了人CD34+细胞培养体系。在人CD34+细胞分化为早幼红细胞的第7天,Zfpm-1最初上调,然后在第9天急剧下调。与mock转染细胞相比,Zfpm-1 siRNA转染的造血干细胞中GPA+细胞多20%,且造血转录因子c-myc和c-myb的表达受到抑制,但GATA-1的表达增加。相反,Zfpm-1功能获得的结果与上述功能丧失的结果相反。

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