Formation of the arterial media during vascular development.

J M Thayer, K Meyers, C M Giachelli, S M Schwartz
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Abstract

We are still in the earliest stages of studying the molecular biology of vascular development. Key questions, even simple questions, such as the origin of endothelial precursors from the epiblast or the mesoderm, remain largely unanswered. For the smooth muscle cell, we do not even have a satisfactory molecular definition of cell type, because the known cell type-specific markers generally disappear when these cells are placed in vitro, and even in vivo smooth muscle cells identified by location can be very undifferentiated. A few bright spots illuminate this cloudy prospect. We do have endothelial lineage markers, and, given the powerful tools of promoting analysis, it seems likely that we will soon known a lot more about the identification of the endothelial lineage. It is hoped that this will help us understand how patterns of development of the vessel wall are controlled. Similarly, the failure of our early studies to identify molecules responsible for investment by smooth muscle can be seen as an exciting finding. If platelet-derived growth factor, fibroblast growth factor, and transforming growth factor beta are not expressed until after smooth muscle investment, still other as yet unidentified factors must be present to account for this stage of development of the vessel wall.

血管发育过程中动脉介质的形成
我们仍处于研究血管发育的分子生物学的早期阶段。关键问题,甚至是简单的问题,如内皮细胞前体来自外胚层或中胚层的起源,在很大程度上仍然没有答案。对于平滑肌细胞,我们甚至没有一个令人满意的细胞类型的分子定义,因为已知的细胞类型特异性标记通常在这些细胞体外放置时消失,甚至在体内通过位置识别的平滑肌细胞也可能非常未分化。一些亮点照亮了这一阴云密布的前景。我们确实有内皮细胞谱系标记,并且,考虑到促进分析的强大工具,我们似乎很快就会对内皮细胞谱系的识别了解得更多。希望这将有助于我们了解血管壁的发育模式是如何被控制的。同样,我们的早期研究未能确定负责平滑肌投资的分子,这可以被视为一个令人兴奋的发现。如果血小板衍生的生长因子、成纤维细胞生长因子和转化生长因子β直到平滑肌形成后才表达,那么必须存在其他尚未确定的因素来解释这一血管壁的发育阶段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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