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Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle

机译:在眼外肌的存在与否中眼运动神经的发育

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Purpose: To spatially and temporally define ocular motor nerve development in the presence and absence of extraocular muscles (EOMs). Methods: Myf5cre mice, which in the homozygous state lack EOMs, were crossed to an IslMN:GFP reporter line to fluorescently label motor neuron cell bodies and axons. Embryonic day (E) 11.5 to E15.5 wild-type and Myf5cre/cre:IslMN:GFP whole mount embryos and dissected orbits were imaged by confocal microscopy to visualize the developing oculomotor, trochlear, and abducens nerves in the presence and absence of EOMs. E11.5 and E18.5 brainstems were serially sectioned and stained for Islet1 to determine the fate of ocular motor neurons. Results: At E11.5, all three ocular motor nerves in mutant embryos approached the orbit with a trajectory similar to that of wild-type. Subsequently, while wild-type nerves send terminal branches that contact target EOMs in a stereotypical pattern, the Myf5cre/cre ocular motor nerves failed to form terminal branches, regressed, and by E18.5 two-thirds of their corresponding motor neurons died. Comparisons between mutant and wild-type embryos revealed novel aspects of trochlear and oculomotor nerve development. Conclusions: We delineated mouse ocular motor nerve spatial and temporal development in unprecedented detail. Moreover, we found that EOMs are not necessary for initial outgrowth and guidance of ocular motor axons from the brainstem to the orbit but are required for their terminal branching and survival. These data suggest that intermediate targets in the mesenchyme provide cues necessary for appropriate targeting of ocular motor axons to the orbit, while EOM cues are responsible for terminal branching and motor neuron survival.
机译:目的:在存在和不存在眼外肌(EOM)的情况下,在空间和时间上定义眼运动神经的发育。方法:将纯合子状态缺乏EOM的Myf5cre小鼠与IslMN:GFP报告基因系杂交,以荧光标记运动神经元细胞体和轴突。通过共聚焦显微镜对胚胎日(E)11.5至E15.5野生型和Myf5cre / cre:IslMN:GFP完整坐骨胚胎和解剖的轨道进行成像,以观察在有无EOM的情况下动眼神经,滑车神经和外展神经的发育。连续切片E11.5和E18.5脑干,并进行胰岛1染色以确定眼动神经元的命运。结果:在E11.5时,突变胚胎中的所有三个眼动神经都以与野生型相似的轨迹接近轨道。随后,当野生型神经发送以定型模式接触目标EOM的末端分支时,Myf5cre / cre眼部运动神经未能形成末端分支,退化,并且到E18.5时,三分之二的相应运动神经元死亡。突变和野生型胚胎之间的比较揭示了滑车和动眼神经发育的新方面。结论:我们以前所未有的细节描绘了小鼠眼运动神经的时空发育。此外,我们发现EOMs对于最初的生长和眼动轴突从脑干到眼眶的引导不是必需的,但对于它们的最终分支和生存是必需的。这些数据表明,间充质中的中间靶标提供了适当的眼动轴突靶向眼眶的必要线索,而EOM线索则负责末端分支和运动神经元的存活。

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