Butterfield Natalie C, Qian Chen, Logan Malcolm P O
Division of Developmental Biology, Medical Research Council - National Institute for Medical Research, London, United Kingdom.
Confocal Image Analysis Lab, Medical Research Council - National Institute for Medical Research, London, United Kingdom.
PLoS One. 2017 Jul 26;12(7):e0180453. doi: 10.1371/journal.pone.0180453. eCollection 2017.
The shapes of homologous skeletal elements in the vertebrate forelimb and hindlimb are distinct, with each element exquisitely adapted to their divergent functions. Many of the signals and signalling pathways responsible for patterning the developing limb bud are common to both forelimb and hindlimb. How disparate morphologies are generated from common signalling inputs during limb development remains poorly understood. We show that, similar to what has been shown in the chick, characteristic differences in mouse forelimb and hindlimb cartilage morphology are maintained when chondrogenesis proceeds in vitro away from the endogenous limb bud environment. Chondrogenic nodules that form in high-density micromass cultures derived from forelimb and hindlimb buds are consistently different in size and shape. We described analytical tools we have developed to quantify these differences in nodule morphology and demonstrate that characteristic hindlimb nodule morphology is lost in the absence of the hindlimb-restricted limb modifier gene Pitx1. Furthermore, we show that ectopic expression of Pitx1 in the forelimb is sufficient to generate nodule patterns characteristic of the hindlimb. We also demonstrate that hindlimb cells are less adhesive to the tissue culture substrate and, within the limb environment, to the extracellular matrix and to each other. These results reveal autonomously programmed differences in forelimb and hindlimb cartilage precursors of the limb skeleton are controlled, at least in part, by Pitx1 and suggest this has an important role in generating distinct limb-type morphologies. Our results demonstrate that the micromass culture system is ideally suited to study cues governing morphogenesis of limb skeletal elements in a simple and experimentally tractable in vitro system that reflects in vivo potential.
脊椎动物前肢和后肢中同源骨骼元件的形状各不相同,每个元件都能完美地适应其不同的功能。许多负责调控发育中肢体芽模式的信号和信号通路在前肢和后肢中是相同的。在肢体发育过程中,如何从共同的信号输入产生不同的形态,目前仍知之甚少。我们发现,与在鸡身上的研究结果类似,当软骨形成在体外远离内源性肢体芽环境的情况下进行时,小鼠前肢和后肢软骨形态的特征性差异得以保留。源自前肢和后肢芽的高密度微团培养物中形成的软骨结节在大小和形状上始终存在差异。我们描述了我们开发的分析工具,用于量化结节形态的这些差异,并证明在缺乏后肢特异性肢体修饰基因Pitx1的情况下,后肢结节的特征形态会消失。此外,我们表明,在前肢中异位表达Pitx1足以产生后肢特有的结节模式。我们还证明,后肢细胞对组织培养底物的粘附性较低,并且在肢体环境中,对细胞外基质和彼此的粘附性也较低。这些结果揭示了肢体骨骼前肢和后肢软骨前体中自主编程的差异至少部分受Pitx1控制,并表明这在产生不同的肢体类型形态中起重要作用。我们的结果表明,微团培养系统非常适合在一个简单且易于实验操作的体外系统中研究控制肢体骨骼元件形态发生的线索,该系统反映了体内的潜能。