Department of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA; email:
Annu Rev Vis Sci. 2021 Sep 15;7:827-850. doi: 10.1146/annurev-vision-093019-114307. Epub 2021 Jun 3.
Abnormalities in cranial motor nerve development cause paralytic strabismus syndromes, collectively referred to as congenital cranial dysinnervation disorders, in which patients cannot fully move their eyes. These disorders can arise through one of two mechanisms: () defective motor neuron specification, usually by loss of a transcription factor necessary for brainstem patterning, or () axon growth and guidance abnormalities of the oculomotor, trochlear, and abducens nerves. This review focuses on our current understanding of axon guidance mechanisms in the cranial motor nerves and how disease-causing mutations disrupt axon targeting. Abnormalities of axon growth and guidance are often limited to a single nerve or subdivision, even when the causative gene is ubiquitously expressed. Additionally, when one nerve is absent, its normal target muscles attract other motor neurons. Study of these disorders highlights the complexities of axon guidance and how each population of neurons uses a unique but overlapping set of axon guidance pathways.
颅神经运动发育异常导致麻痹性斜视综合征,统称为先天性颅神经发育不良障碍,患者无法完全移动眼球。这些疾病可能由以下两种机制之一引起:(1)运动神经元特化缺陷,通常是由于缺失了对脑干模式形成所必需的转录因子,或(2)动眼神经、滑车神经和展神经的轴突生长和导向异常。本综述重点介绍了我们目前对颅神经轴突导向机制的理解,以及致病突变如何破坏轴突靶向。即使在致病基因广泛表达的情况下,轴突生长和导向的异常也常常局限于单一神经或细分。此外,当一条神经缺失时,其正常的靶肌肉会吸引其他运动神经元。对这些疾病的研究突出了轴突导向的复杂性,以及每个神经元群体如何使用独特但重叠的轴突导向途径。