Woronowicz Katherine C, Gline Stephanie E, Herfat Safa T, Fields Aaron J, Schneider Richard A
Department of Orthopaedic Surgery, University of California, San Francisco, 513 Parnassus Avenue, S-1161, San Francisco, CA 94143-0514, USA.
Department of Orthopaedic Surgery, University of California, San Francisco, 513 Parnassus Avenue, S-1161, San Francisco, CA 94143-0514, USA.
Dev Biol. 2018 Dec 1;444 Suppl 1(Suppl 1):S219-S236. doi: 10.1016/j.ydbio.2018.05.002. Epub 2018 May 16.
How does form arise during development and change during evolution? How does form relate to function, and what enables embryonic structures to presage their later use in adults? To address these questions, we leverage the distinct functional morphology of the jaw in duck, chick, and quail. In connection with their specialized mode of feeding, duck develop a secondary cartilage at the tendon insertion of their jaw adductor muscle on the mandible. An equivalent cartilage is absent in chick and quail. We hypothesize that species-specific jaw architecture and mechanical forces promote secondary cartilage in duck through the differential regulation of FGF and TGFβ signaling. First, we perform transplants between chick and duck embryos and demonstrate that the ability of neural crest mesenchyme (NCM) to direct the species-specific insertion of muscle and the formation of secondary cartilage depends upon the amount and spatial distribution of NCM-derived connective tissues. Second, we quantify motility and build finite element models of the jaw complex in duck and quail, which reveals a link between species-specific jaw architecture and the predicted mechanical force environment. Third, we investigate the extent to which mechanical load mediates FGF and TGFβ signaling in the duck jaw adductor insertion, and discover that both pathways are mechano-responsive and required for secondary cartilage formation. Additionally, we find that FGF and TGFβ signaling can also induce secondary cartilage in the absence of mechanical force or in the adductor insertion of quail embryos. Thus, our results provide novel insights on molecular, cellular, and biomechanical mechanisms that couple musculoskeletal form and function during development and evolution.
在发育过程中形态是如何形成的,又是如何在进化过程中发生变化的?形态与功能之间有怎样的关系,是什么使胚胎结构预示着它们在成体中的后期用途?为了解决这些问题,我们利用了鸭、鸡和鹌鹑颌骨独特的功能形态。与它们特殊的进食方式相关,鸭在下颌骨的颌内收肌肌腱插入处发育出一块次生软骨。鸡和鹌鹑则没有这种对应的软骨。我们假设物种特异性的颌骨结构和机械力通过FGF和TGFβ信号的差异调节促进鸭次生软骨的形成。首先,我们在鸡和鸭胚胎之间进行移植,并证明神经嵴间充质(NCM)引导肌肉进行物种特异性插入和次生软骨形成的能力取决于NCM衍生结缔组织的数量和空间分布。其次,我们量化了鸭和鹌鹑颌复合体的运动性并建立了有限元模型,这揭示了物种特异性颌骨结构与预测的机械力环境之间的联系。第三,我们研究了机械负荷在鸭颌内收肌插入处介导FGF和TGFβ信号的程度,并发现这两条途径都对机械力有反应,且是次生软骨形成所必需的。此外,我们发现FGF和TGFβ信号在没有机械力的情况下或在鹌鹑胚胎的内收肌插入处也能诱导次生软骨形成。因此,我们的数据为发育和进化过程中肌肉骨骼形态与功能耦合的分子、细胞和生物力学机制提供了新的见解。