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胚胎造血细胞和内皮细胞的CD34表达不需要c-Myb。

CD34 expression by embryonic hematopoietic and endothelial cells does not require c-Myb.

作者信息

Krause D S, Mucenski M L, Lawler A M, May W S

机构信息

Johns Hopkins Oncology Center and Department of Gynecology and Obstetrics, Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

Exp Hematol. 1998 Oct;26(11):1086-92.

PMID:9766450
Abstract

CD34 is a cell-surface glycoprotein expressed in a developmental, stage-specific manner by bone marrow stem and progenitor cells. In this study we explored a possible role for c-Myb in CD34 regulation during developmental hematopoiesis. The results indicate that c-Myb can induce CD34 expression in hematopoietic and nonhematopoietic cells, and that murine CD34 promoter activity is enhanced in myeloid cells transgenic for c-Myb. To test whether c-Myb is necessary for CD34 expression during developmental hematopoiesis in vitro, c-Myb-null D3 embryonic stem (ES) cells were analyzed for their ability to develop CD34+ hematopoietic cells in vitro. CD34 promoter activity in transient transfections and CD34 upregulation during ES cell differentiation into embryoid bodies was identical in wild-type and c-Myb-null ES cells, indicating that c-Myb is not required for CD34 expression. CD34 protein is expressed on both hematopoietic and endothelial cells of the E8.5 blood islands during the development of c-Myb-null embryos, and expression is nearly identical in wild-type and c-Myb-null embryos. However, in E12.5 c-Myb-null embryos, the majority of identifiable CD34+ cells in the developing liver are endothelial rather than hematopoietic, which is consistent with the absence of colony-forming units in c-Myb-null embryos and developing ES cells. These data indicate that c-Myb is not required for CD34 expression in endothelial or primitive hematopoietic cells in the yolk sac, but is necessary for definitive hematopoiesis.

摘要

CD34是一种细胞表面糖蛋白,由骨髓干细胞和祖细胞以发育阶段特异性的方式表达。在本研究中,我们探讨了c-Myb在发育性造血过程中对CD34调控的可能作用。结果表明,c-Myb可诱导造血细胞和非造血细胞中CD34的表达,并且在转染了c-Myb的髓系细胞中,小鼠CD34启动子活性增强。为了检测c-Myb在体外发育性造血过程中对CD34表达是否必要,分析了c-Myb基因缺失的D3胚胎干细胞(ES细胞)在体外发育为CD34+造血细胞的能力。在野生型和c-Myb基因缺失的ES细胞中,瞬时转染时的CD34启动子活性以及ES细胞分化为胚状体过程中CD34的上调情况相同,这表明CD34表达不需要c-Myb。在c-Myb基因缺失胚胎发育过程中,E8.5血岛的造血细胞和内皮细胞上均表达CD34蛋白,并且在野生型和c-Myb基因缺失胚胎中的表达几乎相同。然而,在E12.5的c-Myb基因缺失胚胎中,发育中的肝脏中大多数可识别的CD34+细胞是内皮细胞而非造血细胞,这与c-Myb基因缺失胚胎和发育中的ES细胞中缺乏集落形成单位一致。这些数据表明,卵黄囊内皮细胞或原始造血细胞中CD34表达不需要c-Myb,但对确定性造血是必要的。

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