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骨形态发生蛋白4(BMP4)和头蛋白通过对血管内皮生长因子受体2(VEGFR-2,即Quek1)表达的拮抗调节来控制胚胎血管形成。

BMP4 and noggin control embryonic blood vessel formation by antagonistic regulation of VEGFR-2 (Quek1) expression.

作者信息

Nimmagadda Suresh, Geetha Loganathan Poongodi, Huang Ruijin, Scaal Martin, Schmidt Corina, Christ Bodo

机构信息

Institute of Anatomy and Cell Biology II, University of Freiburg, Albertstrasse 17, D-79104 Freiburg, Germany.

出版信息

Dev Biol. 2005 Apr 1;280(1):100-10. doi: 10.1016/j.ydbio.2005.01.005.

Abstract

Regulation of VEGFR-2 (Quek1) is an important mechanism during blood vessel formation. In the paraxial mesoderm, Quek1 expression is restricted to the lateral portion of the somite and later to sclerotomal cells surrounding the neural tube. By grafting of either intermediate mesoderm or BMP4 beads into the paraxial mesoderm, we show that BMP4 is a positive regulator of VEGFR-2 (Quek1) expression in the quail embryo. Separation of somites from intermediate mesoderm leads to down-regulation of Quek1 expression. The expression of Quek1 in the medial somite half is normally repressed by the notochord and becomes up-regulated and lateromedially expanded after separation of the notochord. Our results show that up-regulation of BMP4 leads to an increase of the number of blood vessels, whereas inhibition of BMP4 by noggin results in a reduction of blood vessels.

摘要

血管内皮生长因子受体-2(Quek1)的调控是血管形成过程中的一个重要机制。在轴旁中胚层,Quek1的表达局限于体节的外侧部分,随后局限于围绕神经管的硬骨细胞。通过将中间中胚层或BMP4珠移植到轴旁中胚层,我们发现BMP4是鹌鹑胚胎中VEGFR-2(Quek1)表达的正调控因子。体节与中间中胚层分离会导致Quek1表达下调。正常情况下,体节内侧半部中Quek1的表达受到脊索的抑制,在脊索分离后,其表达上调并向外侧扩展。我们的结果表明,BMP4上调会导致血管数量增加,而noggin抑制BMP4则会导致血管数量减少。

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