Ehrman L A, Yutzey K E
Division of Molecular Cardiovascular Biology, The Children's Hospital Research Foundation, 3333 Burnet Avenue, Cincinnati, Ohio, 45229, USA.
Dev Biol. 1999 Mar 1;207(1):163-75. doi: 10.1006/dbio.1998.9167.
The ability to regenerate a heart after ablation of cardiogenic mesoderm has been demonstrated in early stage fish and amphibian embryos but this type of regulation of the heart field has not been seen in avians or mammals. The regulative potential of the cardiogenic mesoderm was examined in avian embryos and related to the spatial expression of genes implicated in early cardiogenesis. With the identification of early cardiac regulators such as bmp-2 and nkx-2.5, it is now possible to reconcile classical embryological studies with molecular mechanisms of cardiac lineage determination in vivo. The most anterior lateral embryonic cells were identified as the region that becomes the heart and removal of all or any subset of these cells resulted in the loss of corresponding cardiac structures. In addition, removal of the lateral heart forming mesoderm while leaving the lateral endoderm intact also results in loss of cardiac structures. Thus the medial anterior mesoderm cannot be recruited into the heart lineage in vivo even in the presence of potentially cardiac inducing endoderm. In situ analysis demonstrated that genes involved in early events of cardiogenesis such as bone morphogenetic protein 2 (bmp-2) and nkx-2.5 are expressed coincidentally with the mapped far lateral heart forming region. The activin type IIa receptor (actR-IIa) is a potential mediator of BMP signaling since it is expressed throughout the anterior mesoderm with the highest level of expression occurring in the lateral prospective heart cells. The posterior boundary of actR-IIa is consistent with the posterior boundary of nkx-2.5 expression, supporting a model whereby ActR-IIa is involved in restricting the heart forming region to an anterior subset of lateral cells exposed to BMP-2. Analysis of the cardiogenic potential of the lateral plate mesoderm posterior to nkx-2.5 and actR-IIa expression demonstrated that these cells are not cardiogenic in vitro and that removal of these cells from the embryo does not result in loss of heart tissue in vivo. Thus, the region of the avian embryo that will become the heart is defined medially, laterally, and posteriorly by nkx-2.5 gene expression. Removal of all or part of the nkx-2.5 expressing region results in the loss of corresponding heart structures, demonstrating the inability of the chick embryo to regenerate cardiac tissue in vivo at stages after nkx-2.5 expression is initiated.
在鱼类和两栖类胚胎的早期阶段,已经证明了心源性中胚层消融后心脏再生的能力,但在鸟类或哺乳动物中尚未观察到这种对心脏区域的调控类型。在鸟类胚胎中研究了心源性中胚层的调控潜力,并将其与早期心脏发生中相关基因的空间表达联系起来。随着早期心脏调节因子如bmp-2和nkx-2.5的鉴定,现在有可能将经典胚胎学研究与体内心脏谱系确定的分子机制协调起来。最前侧的胚胎细胞被确定为形成心脏的区域,去除这些细胞的全部或任何子集都会导致相应心脏结构的缺失。此外,去除形成心脏的外侧中胚层而保留外侧内胚层完整也会导致心脏结构的缺失。因此,即使存在潜在的心脏诱导内胚层,内侧前中胚层在体内也不能被招募到心脏谱系中。原位分析表明,参与心脏发生早期事件的基因,如骨形态发生蛋白2(bmp-2)和nkx-2.5,与映射的最外侧心脏形成区域同时表达。激活素IIa型受体(actR-IIa)是BMP信号的潜在介导因子,因为它在前中胚层中全程表达,在外侧预期心脏细胞中的表达水平最高。actR-IIa的后边界与nkx-2.5表达的后边界一致,支持了一个模型,即ActR-IIa参与将心脏形成区域限制在暴露于BMP-2的外侧细胞的前侧子集中。对nkx-2.5和actR-IIa表达后侧的侧板中胚层的心脏发生潜力分析表明,这些细胞在体外没有心脏发生能力,并且从胚胎中去除这些细胞不会导致体内心脏组织的缺失。因此,鸟类胚胎中将要形成心脏的区域在内侧、外侧和后侧由nkx-2.5基因表达来界定。去除全部或部分表达nkx-2.5的区域会导致相应心脏结构的缺失,这表明在nkx-2.5表达开始后的阶段,鸡胚在体内无法再生心脏组织。