Tickle Cheryll
Department of Biology and Biochemistry, University of Bath, Bath, UK.
J Anat. 2015 Oct;227(4):418-30. doi: 10.1111/joa.12361. Epub 2015 Aug 7.
The vertebrate limb with its complex anatomy develops from a small bud of undifferentiated mesoderm cells encased in ectoderm. The bud has its own intrinsic polarity and can develop autonomously into a limb without reference to the rest of the embryo. In this review, recent advances are integrated with classical embryology, carried out mainly in chick embryos, to present an overview of how the embryo makes a limb bud. We will focus on how mesoderm cells in precise locations in the embryo become determined to form a limb and express the key transcription factors Tbx4 (leg/hindlimb) or Tbx5 (wing/forelimb). These Tbx transcription factors have equivalent functions in the control of bud formation by initiating a signalling cascade involving Wnts and fibroblast growth factors (FGFs) and by regulating recruitment of mesenchymal cells from the coelomic epithelium into the bud. The mesoderm that will form limb buds and the polarity of the buds is determined with respect to both antero-posterior and dorso-ventral axes of the body. The position in which a bud develops along the antero-posterior axis of the body will also determine its identity - wing/forelimb or leg/hindlimb. Hox gene activity, under the influence of retinoic acid signalling, is directly linked with the initiation of Tbx5 gene expression in the region along the antero-posterior axis of the body that will form wings/forelimbs and determines antero-posterior polarity of the buds. In contrast, Tbx4 expression in the regions that will form legs/hindlimbs is regulated by the homeoprotein Pitx1 and there is no evidence that Hox genes determine antero-posterior polarity of the buds. Bone morphogenetic protein (BMP) signalling determines the region along the dorso-ventral axis of the body in which both wings/forelimbs and legs/hindlimbs develop and dorso-ventral polarity of the buds. The polarity of the buds leads to the establishment of signalling regions - the dorsal and ventral ectoderm, producing Wnts and BMPs, respectively, the apical ectodermal ridge producing fibroblast growth factors and the polarizing region, Sonic hedgehog (Shh). These signals are the same in both wings/forelimbs and legs/hindlimbs and control growth and pattern formation by providing the mesoderm cells of the limb bud as it develops with positional information. The precise anatomy of the limb depends on the mesoderm cells in the developing bud interpreting positional information according to their identity - determined by Pitx1 in hindlimbs - and genotype. The competence to form a limb extends along the entire antero-posterior axis of the trunk - with Hox gene activity inhibiting the formation of forelimbs in the interlimb region - and also along the dorso-ventral axis.
脊椎动物具有复杂解剖结构的肢体,是由包裹在外胚层内的一小团未分化中胚层细胞发育而来的。这个芽体有其自身的内在极性,无需参考胚胎的其他部分就能自主发育成肢体。在这篇综述中,主要结合在鸡胚胎中进行的经典胚胎学研究的最新进展,概述胚胎如何形成肢体芽。我们将重点关注胚胎中精确位置的中胚层细胞如何被决定形成肢体,并表达关键转录因子Tbx4(腿/后肢)或Tbx5(翅/前肢)。这些Tbx转录因子在控制芽形成方面具有同等功能,它们通过启动涉及Wnt和成纤维细胞生长因子(FGF)的信号级联反应,并调节间皮细胞从体腔上皮细胞募集到芽体中。将形成肢体芽的中胚层及其极性是相对于身体的前后轴和背腹轴来确定的。芽体沿着身体前后轴发育的位置也将决定其身份——翅/前肢或腿/后肢。在视黄酸信号的影响下,Hox基因活性与身体前后轴上将形成翅/前肢的区域中Tbx5基因表达的起始直接相关,并决定芽体的前后极性。相比之下,将形成腿/后肢的区域中Tbx4的表达受同源结构域蛋白Pitx1调控,没有证据表明Hox基因决定芽体的前后极性。骨形态发生蛋白(BMP)信号决定了身体背腹轴上翅/前肢和腿/后肢发育的区域以及芽体的背腹极性。芽体的极性导致信号区域的建立——背侧和腹侧外胚层,分别产生Wnt和BMP,顶端外胚层嵴产生成纤维细胞生长因子,以及极化区域,即音猬因子(Shh)。这些信号在翅/前肢和腿/后肢中都是相同的,通过在肢体芽发育过程中为中胚层细胞提供位置信息来控制生长和模式形成。肢体的精确解剖结构取决于发育中的芽体中的中胚层细胞根据其身份——由Pitx1在后肢中决定——和基因型来解读位置信息。形成肢体的能力沿着躯干整个前后轴延伸——Hox基因活性抑制肢体间区域前肢的形成——并且也沿着背腹轴延伸。