视网膜神经节细胞轴突再生和生长锥引导的线粒体动力学。

Journal of ocular biology Pub Date : 2013-09-21
Kira L Lathrop, Michael B Steketee
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引用次数: 0

摘要

创伤或疾病(包括青光眼和线粒体视神经病变)后轴突再生失败和视网膜神经节细胞(RGC)死亡越来越多地与线粒体功能障碍相关。线粒体是高度动态的细胞器,其大小、组织和功能受线粒体裂变和融合之间的平衡调节。线粒体在体外和体内以及发育和再生过程中普遍存在于轴突生长锥中。然而,在轴突再生过程中,线粒体裂变和融合动力学在生长锥中所起的作用在很大程度上尚未得到研究。在这里,我们讨论了最近的数据,表明线粒体在远端轴突和生长锥中通过整合轴突的内在生长状态和来自外部信号的信号,在轴突生长中起着核心作用。在具有不同内在轴突生长电位的急性纯化胚胎和出生后RGCs的生长锥中,线粒体裂变和融合在远端轴突受到内在调节。这些裂变和融合的差异与线粒体生物能量学的差异有关;具有高内在轴突生长潜能的胚胎RGCs更多地依赖于糖酵解,而具有低内在轴突生长潜能的胚胎RGCs更多地依赖于氧化磷酸化。线粒体分裂和融合也受到KLFs的不同调节,这些KLFs可以促进或抑制轴突的内在生长,改变线粒体分裂和融合之间的平衡可以不同地调节轴突的生长速度和生长锥对抑制性和许可性引导信号的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitochondrial Dynamics in Retinal Ganglion Cell Axon Regeneration and Growth Cone Guidance.

Failed axon regeneration and retinal ganglion cell (RGC) death after trauma or disease, including glaucomatous and mitochondrial optic neuropathies, are increasingly linked to mitochondrial dysfunction. Mitochondria are highly dynamic organelles whose size, organization, and function are regulated by a balance between mitochondrial fission and fusion. Mitochondria are ubiquitous in axonal growth cones both in vitro and in vivo and during development and regeneration. However, the roles that mitochondrial fission and fusion dynamics play in the growth cone during axon regeneration are largely unstudied. Here we discuss recent data suggesting mitochondria in the distal axon and growth cone play a central role in axon growth by integrating intrinsic axon growth states with signaling from extrinsic cues. Mitochondrial fission and fusion are intrinsically regulated in the distal axon in the growth cones of acutely purified embryonic and postnatal RGCs with differing intrinsic axon growth potentials. These differences in fission and fusion correlate with differences in mitochondrial bioenergetics; embryonic RGCs with high intrinsic axon growth potential rely more on glycolysis whereas RGCs with low intrinsic axon growth potential rely more on oxidative phosphorylation. Mitochondrial fission and fusion are also differentially modulated by KLFs that either promote or suppress intrinsic axon growth, and altering the balance between mitochondrial fission and fusion can differentially regulate axon growth rate and growth cone guidance responses to both inhibitory and permissive guidance cues.

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