Department of Developmental Biology, Institute of Experimental Medicine of the Czech Academy of Sciences, Praha, Czech Republic.
Department of Cell Biology, Faculty of Science, Charles University, Praha, Czech Republic.
Biol Open. 2020 Jul 2;9(6):bio052043. doi: 10.1242/bio.052043.
Cranial neural crest cells (cNCCs) originate in the anterior neural tube and populate pharyngeal arches in which they contribute to formation of bone and cartilage. This cell population also provides molecular signals for the development of tissues of non-neural crest origin, such as the tongue muscles, teeth enamel or gland epithelium. Here we show that the transcription factor Meis2 is expressed in the oral region of the first pharyngeal arch (PA1) and later in the tongue primordium. Conditional inactivation of in cNCCs resulted in loss of Sonic hedgehog signalling in the oropharyngeal epithelium and impaired patterning of PA1 along the lateral-medial and oral-aboral axis. Failure of molecular specification of PA1, illustrated by altered expression of , , , and other markers, led to hypoplastic tongue and ectopic ossification of the mandible. -mutant mice thus display craniofacial defects that are reminiscent of several human syndromes and patients with mutations in the gene.
颅神经嵴细胞(cNCCs)起源于前神经管,并定位于咽弓中,在那里它们有助于骨和软骨的形成。这群细胞还为非神经嵴起源的组织的发育提供分子信号,如舌肌、牙齿釉质或腺上皮。在这里,我们表明转录因子 Meis2 在第一咽弓(PA1)的口腔区域表达,然后在舌原基中表达。cNCCs 中的条件性缺失导致口咽上皮中的 Sonic hedgehog 信号转导丧失,并沿着侧向-中轴和口腔-口轴的 PA1 模式形成受损。PA1 的分子特征丧失,表现为 、 、 、 和其他标记物的表达改变,导致舌发育不良和下颌骨异位骨化。因此, -突变小鼠表现出颅面缺陷,类似于几种人类综合征和 基因突变患者。