Micromanaging Palate Development.

David E Clouthier, Josie Gray, Kristin Bruk Artinger
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引用次数: 3

Abstract

Development of the facial skeleton is one of the most intriguing and intricate events that occur during human development. Most of the bone, cartilage and connective tissue that compose the face and neck arise from a class of cells, referred to as neural crest cells, which are initially located at some distance from the facial primordium. A complex set of events regulated by specific gene products direct the formation, migration and differentiation of these cells, leading to what is viewed as "prototypical" adult facial features. These basic developmental processes are recapitulated during the formation of the palate, termed palatogenesis. In this review, we summarize the basic embryology leading to palate formation, discuss mechanisms that can lead to palatal dysmorphologies and highlight a new interaction that has recently been demonstrated to play a role in palate development. This interaction, involving small non-coding RNAs referred to as microRNAs, not only establishes a new level of regulation to cellular development, but may also serve as attractive targets for future efforts directed at clinical treatment of birth defect syndromes.

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微观管理上颚发育。
面部骨骼的发育是人类发育过程中最有趣、最复杂的事件之一。构成面部和颈部的大部分骨骼、软骨和结缔组织都是由一类被称为神经嵴细胞的细胞产生的,这些细胞最初位于距离面部原基一定距离的地方。由特定基因产物调控的一系列复杂事件指导这些细胞的形成、迁移和分化,导致被视为“原型”的成人面部特征。这些基本的发育过程在上颚的形成过程中重演,称为腭发育。在这篇综述中,我们总结了导致腭形成的基本胚胎学,讨论了导致腭畸形的机制,并强调了最近被证明在腭发育中起作用的一种新的相互作用。这种涉及小的非编码rna(称为microrna)的相互作用,不仅建立了对细胞发育的新水平的调控,而且可能成为未来针对出生缺陷综合征临床治疗的有吸引力的靶点。
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