Damon Brooke J, Mezentseva Nadejda V, Kumaratilake Jaliya S, Forgacs Gabor, Newman Stuart A
Department of Physics and Astronomy, University of Missouri-Columbia, Columbia, MO 65211, USA.
Dev Biol. 2008 Sep 15;321(2):319-30. doi: 10.1016/j.ydbio.2008.06.018. Epub 2008 Jun 20.
Limb bud outgrowth in chicken embryos is initiated during the third day of development by Fibroblast Growth Factor 8 (FGF8) produced by the newly formed apical ectodermal ridge (AER). One of the earliest effects of this induction is a change in the properties of the limb field mesoderm leading to bulging of the limb buds from the body wall. Heintzelman et al. [Heintzelman, K.F., Phillips, H.M., Davis, G.S., 1978. Liquid-tissue behavior and differential cohesiveness during chick limb budding. J. Embryol. Exp. Morphol. 47, 1-15.] suggested that budding of the limbs is caused by a higher liquid-like cohesivity of limb bud tissue compared with flank. We sought additional evidence relevant to this hypothesis by performing direct measurements of the effective surface tension, a measure of relative tissue cohesivity, of 4-day embryonic chicken wing and leg bud mesenchymal tissue, and adjacent flank mesoderm. As predicted, the two types of limb tissues were 1.5- to 2-fold more cohesive than the flank tissue. These differences paralleled cell number and volume density differences: 4-day limb buds had 2- to 2.5-fold as many cells per unit area of tissue as surrounding flank, a difference also seen at 3 days, when limb budding begins. Exposure of flank tissue to exogenous FGF8 for 24 h increased its cell number and raised its cohesivity to limb-like values. Four-day flank tissue exhibited a novel and unique active rebound response to compression, which was suppressed by the drug latrunculin and therefore dependent on an intact actin cytoskeleton. Correspondingly, flank at this stage expressed high levels of alpha-smooth muscle actin (SMA) mRNA and protein and a dense network of microfilaments. Treatment of flank with FGF8 eliminated the rebound response. We term material properties of tissues, such as cohesivity and mechanical excitability, the "physical phenotype", and propose that changes thereof are driving forces of morphogenesis. Our results indicate that two independent aspects of the physical phenotype of flank mesoderm can be converted to a limb-like state in response to treatment with FGF8. The higher tissue cohesivity induced by this effect will cause the incipient limb bud to phase separate from the surrounding flank, while the active mechanical response of the flank could help ensure that the limb bud bulges out from, rather than becoming engulfed by, this less cohesive tissue.
鸡胚肢体芽的生长在发育的第三天由新形成的顶端外胚层嵴(AER)产生的成纤维细胞生长因子8(FGF8)启动。这种诱导的最早效应之一是肢体场中胚层特性的改变,导致肢体芽从体壁突出。海因策尔曼等人[海因策尔曼,K.F.,菲利普斯,H.M.,戴维斯,G.S.,1978年。鸡胚肢体出芽过程中的液体-组织行为和差异黏附性。《胚胎学与实验形态学杂志》47,1-15。]认为,肢体出芽是由于肢体芽组织与胁腹相比具有更高的类液体黏附性。我们通过直接测量4日龄鸡胚鸡翅和鸡腿芽间充质组织以及相邻胁腹中胚层的有效表面张力(一种相对组织黏附性的度量),来寻找与该假设相关的更多证据。正如所预测的,这两种类型的肢体组织的黏附性比胁腹组织高1.5至2倍。这些差异与细胞数量和体积密度差异平行:4日龄肢体芽每单位组织面积的细胞数量是周围胁腹的2至2.5倍,这种差异在肢体出芽开始的3日龄时也可见。将胁腹组织暴露于外源性FGF8 24小时会增加其细胞数量,并将其黏附性提高到类似肢体的水平。4日龄胁腹组织对压缩表现出一种新的独特的主动反弹反应,这种反应被药物拉春库林抑制,因此依赖于完整的肌动蛋白细胞骨架。相应地,这个阶段的胁腹表达高水平的α-平滑肌肌动蛋白(SMA)mRNA和蛋白质以及密集的微丝网络。用FGF8处理胁腹消除了反弹反应。我们将组织的物质特性,如黏附性和机械兴奋性,称为“物理表型”,并提出其变化是形态发生的驱动力。我们的结果表明,胁腹中胚层物理表型的两个独立方面可以通过用FGF8处理而转变为类似肢体的状态。这种效应诱导的更高组织黏附性将导致初始肢体芽与周围胁腹相分离,而胁腹的主动机械反应有助于确保肢体芽从这种黏附性较低的组织中突出,而不是被其吞噬。