Department of Molecular Biosciences, University of Texas at Austin, Austin, TX, USA.
Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Methods Mol Biol. 2022;2438:415-437. doi: 10.1007/978-1-0716-2035-9_24.
Apical constriction refers to the active, actomyosin-driven process that reduces apical cell surface area in epithelial cells. Apical constriction is utilized in epithelial morphogenesis during embryonic development in multiple contexts, such as gastrulation, neural tube closure, and organogenesis. Defects in apical constriction can result in congenital birth defects, yet our understanding of the molecular control of apical constriction is relatively limited. To uncover new genetic regulators of apical constriction and gain mechanistic insight into the cell biology of this process, we need reliable assay systems that allow real-time observation and quantification of apical constriction as it occurs and permit gain- and loss-of-function analyses to explore gene function and interaction during apical constriction. In this chapter, we describe using the early Xenopus embryo as an assay system to investigate molecular mechanisms involved in apical constriction during both gastrulation and neurulation.
顶端缢缩是指上皮细胞中由肌动球蛋白驱动的主动过程,可减少顶端细胞表面积。在胚胎发育的多个过程中,如原肠胚形成、神经管闭合和器官发生,顶端缢缩被用于上皮形态发生。顶端缢缩的缺陷可能导致先天性出生缺陷,但我们对顶端缢缩的分子控制的理解相对有限。为了揭示顶端缢缩的新的遗传调节因子,并深入了解这一过程的细胞生物学,我们需要可靠的测定系统,允许实时观察和量化发生的顶端缢缩,并允许进行增益和损耗功能分析,以探索顶端缢缩过程中基因的功能和相互作用。在本章中,我们描述了使用早期非洲爪蟾胚胎作为测定系统来研究原肠胚形成和神经胚形成期间参与顶端缢缩的分子机制。