Department of Biology, University of Nevada, Reno, NV, 89557, USA.
Department of Ophthalmology & Visual Science, University of Michigan Medical School, Ann Arbor, MI, 48105, USA.
Dev Biol. 2021 Aug;476:272-281. doi: 10.1016/j.ydbio.2021.04.006. Epub 2021 Apr 24.
Muscle function is dependent on innervation by the correct motor nerves. Motor nerves are composed of motor axons which extend through peripheral tissues as a compact bundle, then diverge to create terminal nerve branches to specific muscle targets. As motor nerves approach their targets, they undergo a transition where the fasciculated nerve halts further growth then after a pause, the nerve later initiates branching to muscles. This transition point is potentially an intermediate target or guidepost to present specific cellular and molecular signals for navigation. Here we describe the navigation of the oculomotor nerve and its association with developing muscles in mouse embryos. We found that the oculomotor nerve initially grew to the eye three days prior to the appearance of any extraocular muscles. The oculomotor axons spread to form a plexus within a mass of cells, which included precursors of extraocular muscles and other orbital tissues and expressed the transcription factor Pitx2. The nerve growth paused in the plexus for more than two days, persisting during primary extraocular myogenesis, with a subsequent phase in which the nerve branched out to specific muscles. To test the functional significance of the nerve contact with Pitx2+ cells in the plexus, we used two strategies to genetically ablate Pitx2+ cells or muscle precursors early in nerve development. The first strategy used Myf5-Cre-mediated expression of diphtheria toxin A to ablate muscle precursors, leading to loss of extraocular muscles. The oculomotor axons navigated to the eye to form the main nerve, but subsequently largely failed to initiate terminal branches. The second strategy studied Pitx2 homozygous mutants, which have early apoptosis of Pitx2-expressing precursor cells, including precursors for extraocular muscles and other orbital tissues. Oculomotor nerve fibers also grew to the eye, but failed to stop to form the plexus, instead grew long ectopic projections. These results show that neither Pitx2 function nor Myf5-expressing cells are required for oculomotor nerve navigation to the eye. However, Pitx2 function is required for oculomotor axons to pause growth in the plexus, while Myf5-expressing cells are required for terminal branch initiation.
肌肉功能依赖于正确的运动神经的支配。运动神经由运动轴突组成,这些轴突穿过外周组织形成一个紧密的束,然后发散形成末端神经分支,到达特定的肌肉靶标。当运动神经接近其靶标时,它们会经历一个转变,即神经束停止进一步生长,然后在停顿后,神经开始分支到肌肉。这个过渡点可能是一个中间靶点或路标,为导航提供特定的细胞和分子信号。在这里,我们描述了动眼神经的导航及其与小鼠胚胎发育中的肌肉的关联。我们发现,动眼神经在眼外肌出现前三天就开始向眼生长。动眼轴突扩散形成一个神经丛,其中包括眼外肌和其他眼眶组织的前体细胞,并表达转录因子 Pitx2。神经生长在神经丛中暂停了两天多,在初级眼外肌发生期间持续存在,随后进入一个分支到特定肌肉的阶段。为了测试神经与神经丛中 Pitx2+细胞接触的功能意义,我们使用两种策略在神经发育早期遗传消融 Pitx2+细胞或肌肉前体细胞。第一种策略使用 Myf5-Cre 介导的白喉毒素 A 的表达来消融肌肉前体细胞,导致眼外肌缺失。动眼神经轴突向眼生长形成主要神经,但随后大部分未能启动末端分支。第二种策略研究了 Pitx2 纯合突变体,其 Pitx2 表达前体细胞包括眼外肌和其他眼眶组织的前体细胞发生早期凋亡。动眼神经纤维也向眼生长,但未能停止形成神经丛,而是生长出长的异位突起。这些结果表明,Pitx2 功能或表达 Myf5 的细胞对于动眼神经向眼的导航都不是必需的。然而,Pitx2 功能对于动眼神经轴突在神经丛中停止生长是必需的,而表达 Myf5 的细胞对于末端分支的起始是必需的。