Department of Pharmacology and Experimental Therapeutics, Boston University Aram V. Chobanian & Edward Avedisian School of Medicine, Boston, MA, United States.
Department of Orthopaedic Surgery, Boston Children's Hospital, Boston, MA, United States.
Front Endocrinol (Lausanne). 2022 Nov 1;13:969481. doi: 10.3389/fendo.2022.969481. eCollection 2022.
Efforts to understand the morphogenesis of complex craniofacial structures have largely focused on the role of chondrocytes and osteoblasts. Along with these bone-creating cells, bone-resorbing osteoclasts are critical in homeostasis of adult skeletal structures, but there is currently limited information on their role in the complex morphogenetic events of craniofacial development. Fundamental aspects of skull formation and general skeletal development are conserved from zebrafish to mammals. Using a reporter, we documented osteoclast location in the developing zebrafish skull over several weeks, from 5.18 mm to 9.6 mm standard length (approximately 15 to 34 days post fertilization). While broad distribution of osteoclasts is consistent across individuals, they are sparse and the exact locations vary among fish and across developmental time points. Interestingly, we observed osteoclasts concentrating at areas associated with neuromasts and their associated nerves, in particular the hyomandibular foramina and around the supraorbital lateral line. These are areas of active remodeling. In contrast, other areas of rapid bone growth, such as the osteogenic fronts of the frontal and parietal bones, show no particular concentration of osteoclasts, suggesting that they play a special role in shaping bone near neuromasts and nerves. In mutants lacking functional osteoclasts, the morphology of the cranial bone was disrupted in both areas. The hyomandibular foramen is present in the initial cartilage template, but after the initiation of ossification, the diameter of the canal is significantly smaller in the absence of osteoclasts. The diameter of the supraorbital lateral line canals was also reduced in the mutants, as was the number of pores associated with neuromasts, which allow for the passage of associated nerves through the bone. Our findings define important and previously unappreciated roles for osteoclast activity in shaping craniofacial skeletal structures with a particular role in bone modeling around peripheral cranial nerves, providing a scaffold for wiring the sensioneural system during craniofacial development. This has important implications for the formation of the evolutionarily diverse lateral line system, as well understanding the mechanism of neurologic sequelae of congenital osteoclast dysfunction in human craniofacial development.
人们为了理解复杂颅面结构的形态发生,主要关注软骨细胞和成骨细胞的作用。除了这些造骨细胞,破骨细胞在成体骨骼结构的动态平衡中也起着至关重要的作用,但目前关于其在颅面发育的复杂形态发生事件中的作用的信息有限。从斑马鱼到哺乳动物,颅骨形成和一般骨骼发育的基本方面都是保守的。我们使用一个报告基因,在从 5.18 毫米到 9.6 毫米标准体长(约受精后 15 到 34 天)的几个星期内,记录了发育中的斑马鱼颅骨中破骨细胞的位置。尽管破骨细胞在个体间广泛分布,但它们稀疏且在不同鱼类和不同发育时间点的位置各不相同。有趣的是,我们观察到破骨细胞集中在与神经丘及其相关神经相关的区域,特别是在舌下骨孔和眶上侧线周围。这些是活跃重塑的区域。相比之下,其他快速骨生长区域,如额骨和顶骨的成骨前缘,没有特别集中的破骨细胞,这表明它们在塑造神经丘和神经附近的骨骼方面发挥着特殊作用。在缺乏功能性破骨细胞的 突变体中,颅骨的形态在这两个区域都受到了破坏。舌下骨孔存在于初始软骨模板中,但在骨化开始后,在没有破骨细胞的情况下,管的直径明显变小。眶上侧线管的直径在突变体中也减小了,与神经丘相关的孔的数量也减少了,这些孔允许相关神经穿过骨骼。我们的发现定义了破骨细胞活性在塑造颅面骨骼结构方面的重要且以前未被认识到的作用,特别是在外周颅神经周围的骨建模中发挥作用,为颅面发育过程中感觉神经系统的布线提供了支架。这对进化上多样化的侧线系统的形成以及理解人类颅面发育中先天性破骨细胞功能障碍的神经后遗症的机制都具有重要意义。