Polarized expression of bone morphogenetic protein-4 in the human aorta-gonad-mesonephros region

被引:94
作者
Marshall, CJ [1 ]
Kinnon, C [1 ]
Thrasher, AJ [1 ]
机构
[1] Inst Child Hlth, Mol Immunol Unit, London WC1N 1EH, England
基金
英国医学研究理事会;
关键词
D O I
10.1182/blood.V96.4.1591.h8001591_1591_1593
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the mammal, definitive hematopoietic stem cells (HSCs) are first derived from mesodermal cells within a region of the embryonic para-aortic splanchnopleura known as the aorta-gonad-mesonephros (AGM), Within this region, HSCs are thought to arise from hemangioblast precursors located in the ventral wall of the dorsal aorta. However, the factors that regulate HSC development in vivo are still largely unknown, Bone morphogenetic protein (BMP)-4, a member of the transforming growth factor beta (TGF-beta) superfamily of growth factors, is a potent ventralizing factor and has been implicated in the commitment of embryonic mesodermal cells to a hematopoietic fate in a number of systems. In the human AGM, we find that BMP-4 is expressed at high levels, and with striking polarity, in a region of densely packed cells underlying intra-aortic hematopoietic clusters. In contrast, TGF-beta 1 is expressed predominantly by hematopoietic cells within the clusters. These findings implicate both BMP-4 and TGF-beta 1 in the initiation and regulation of hematopoiesis in the human AGM, Furthermore, the distribution of BMP-4 expression is highly suggestive of a direct role in the specification of human hematopoietic cells from embryonic mesoderm in vivo.(Blood. 2000;96:1591-1593) (C) 2000 by The American Society of Hematology.
引用
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页码:1591 / 1593
页数:3
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