Caiaffa Carlo Donato, Ambekar Yogeshwari S, Singh Manmohan, Lin Ying Linda, Wlodarczyk Bogdan, Aglyamov Salavat R, Scarcelli Giuliano, Larin Kirill V, Finnell Richard
bioRxiv. 2023 Aug 4:2023.08.04.552068. doi: 10.1101/2023.08.04.552068.
The formation of the brain and spinal cord is initiated in the earliest stages of mammalian pregnancy in a highly organized process known as neurulation. Convergent and extension movements transforms a flat sheet of ectodermal cells into a narrow and elongated line of neuroepithelia, while a major source of Sonic Hedgehog signaling from the notochord induces the overlying neuroepithelial cells to form two apposed neural folds. Afterward, neural tube closure occurs by synchronized coordination of the surface ectoderm and adjacent neuroepithelial walls at specific axial regions known as neuropores. Environmental or genetic interferences can impair neurulation resulting in neural tube defects. The gene encodes a subunit of the CPLANE complex, which is a macromolecular planar polarity effector required for ciliogenesis. Ablation of in mouse embryos results in exencephaly and spina bifida, including dysmorphic craniofacial structures due to defective cilia formation and impaired Sonic Hedgehog signaling. In this work, we demonstrate that knocking out during embryonic mouse development results in a hypoplastic hindbrain phenotype, displaying abnormal rhombomeres with reduced length and width. This phenotype is associated with persistent loss of ventral neuroepithelial stiffness, in a notochord adjacent area at the level of the rhombomere 5, preceding the development of exencephaly in ablated mutants. The formation of cranial and paravertebral ganglia is also impaired in these embryos, indicating that has a critical function sustaining normal neural tube development and neuronal differentiation.
Neural tube defects (NTDs) are a common cause of disability in children, representing the second most common congenital structural malformation in humans following only congenital cardiovascular malformations. NTDs affect approximately 1 to 2 pregnancies per 1000 births every year worldwide, when the mechanical forces folding the neural plate fails to close at specific neuropores located anteriorly (cranial) or posteriorly (caudal) along the neural tube, in a process known as neurulation, which happens throughout the third and fourth weeks of human pregnancy.
大脑和脊髓的形成在哺乳动物怀孕的最早阶段就开始了,这是一个高度有序的过程,称为神经胚形成。汇聚和延伸运动将一层扁平的外胚层细胞转化为一条狭窄且细长的神经上皮细胞线,而来自脊索的音猬因子信号的主要来源诱导上方的神经上皮细胞形成两个相对的神经褶。之后,神经管闭合通过表面外胚层和相邻神经上皮壁在特定轴向区域(称为神经孔)的同步协调而发生。环境或基因干扰会损害神经胚形成,导致神经管缺陷。该基因编码CPLANE复合体的一个亚基,CPLANE复合体是纤毛发生所需的一种大分子平面极性效应器。在小鼠胚胎中敲除该基因会导致无脑畸形和脊柱裂,包括由于纤毛形成缺陷和音猬因子信号受损导致的颅面结构畸形。在这项研究中,我们证明在胚胎小鼠发育过程中敲除该基因会导致后脑发育不全的表型,表现为异常的菱脑节,其长度和宽度减小。这种表型与菱形节段5水平的脊索相邻区域腹侧神经上皮硬度的持续丧失有关,这发生在敲除突变体无脑畸形出现之前。这些胚胎中颅神经节和椎旁神经节的形成也受到损害,表明该基因在维持正常神经管发育和神经元分化方面具有关键作用。
神经管缺陷(NTDs)是儿童残疾的常见原因,是人类第二常见的先天性结构畸形,仅次于先天性心血管畸形。全世界每年每1000例出生中约有1至2例受NTDs影响,在神经胚形成过程中,折叠神经板的机械力未能在沿神经管前部(颅部)或后部(尾部)的特定神经孔处闭合,神经胚形成发生在人类怀孕的第三和第四周。