Rengasamy Venugopalan Shankar, Van Otterloo Eric
Iowa Institute for Oral Health Research, College of Dentistry, University of Iowa, Iowa City, IA 52242, USA.
Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, IA 52242, USA.
J Dev Biol. 2021 Jan 23;9(1):3. doi: 10.3390/jdb9010003.
The cranial base is a multifunctional bony platform within the core of the cranium, spanning rostral to caudal ends. This structure provides support for the brain and skull vault above, serves as a link between the head and the vertebral column below, and seamlessly integrates with the facial skeleton at its rostral end. Unique from the majority of the cranial skeleton, the cranial base develops from a cartilage intermediate-the chondrocranium-through the process of endochondral ossification. Owing to the intimate association of the cranial base with nearly all aspects of the head, congenital birth defects impacting these structures often coincide with anomalies of the cranial base. Despite this critical importance, studies investigating the genetic control of cranial base development and associated disorders lags in comparison to other craniofacial structures. Here, we highlight and review developmental and genetic aspects of the cranial base, including its transition from cartilage to bone, dual embryological origins, and vignettes of transcription factors controlling its formation.
颅底是颅骨核心内的一个多功能骨平台,从颅前端延伸至尾端。该结构为上方的脑和颅顶提供支撑,是下方头部与脊柱之间的连接,并在其前端与面骨无缝整合。与大多数颅骨不同,颅底由软骨中间体——软骨颅——通过软骨内骨化过程发育而来。由于颅底与头部几乎所有方面都密切相关,影响这些结构的先天性出生缺陷往往与颅底异常同时出现。尽管至关重要,但与其他颅面结构相比,研究颅底发育和相关疾病的遗传控制仍较为滞后。在此,我们重点介绍并综述颅底的发育和遗传方面,包括其从软骨到骨的转变、双重胚胎起源以及控制其形成的转录因子实例。