Patil Ankita, Guha Shrobona, Isiltan Ilgin, Muralidharan Hemalatha, Madugula Kirankumar, Baas Peter W
Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.
Molecular Biology and Genetics Department, Istanbul Technical University, Istanbul, Turkey.
FASEB J. 2025 Jun 15;39(11):e70683. doi: 10.1096/fj.202500675RR.
Microtubules (MTs) in the axon are nearly all oriented with plus-end-out, and this pattern of organization is important for regulating the morphology and cytoplasmic composition of the axon, and for defining the cargoes transported in the anterograde and retrograde directions in the axon. Over the past several years, studies on vertebrate neurons (and also insect neurons) have been conducted by many investigators to understand the mechanisms that establish this pattern and maintain it over the life of the neuron and in the face of potential corruption. Studies on cultured rat sympathetic neurons from superior cervical ganglia (and also insect neurons) have implicated sliding of MTs by cytoplasmic dynein as crucial not only for establishing the plus-end-out orientation of axonal MTs but also for clearing mal-oriented MTs from the axon. Studies on cultured rat hippocampal neurons have implicated TRIM46 and augmin, proteins that regulate the crosslinking and nucleation of MTs, respectively. Here we show that the axons of hippocampal neurons also require dynein-based mechanisms for regulating their MT polarity pattern; however, the axons of sympathetic neurons do not require either TRIM46 or augmin. We also show that, in hippocampal neurons but not sympathetic neurons, the axon's MT polarity pattern is corrupted when a portion of the available Kinesin-1 is pharmacologically shifted from organelle transport to MT sliding. Collectively these results indicate that the mechanisms that regulate the MT polarity pattern of the axon are not entirely the same for different kinds of neurons, even in the same animal.
轴突中的微管几乎都是正端向外排列,这种组织模式对于调节轴突的形态和细胞质组成,以及确定轴突中顺行和逆行方向运输的货物非常重要。在过去几年中,许多研究人员对脊椎动物神经元(以及昆虫神经元)进行了研究,以了解建立这种模式并在神经元的生命周期中以及面对潜在破坏时维持这种模式的机制。对上颈神经节培养的大鼠交感神经元(以及昆虫神经元)的研究表明,细胞质动力蛋白介导的微管滑动不仅对于建立轴突微管的正端向外方向至关重要,而且对于清除轴突中方向错误的微管也至关重要。对培养的大鼠海马神经元的研究表明,TRIM46和augmin分别参与调节微管的交联和成核。在这里,我们表明海马神经元的轴突也需要基于动力蛋白的机制来调节其微管极性模式;然而,交感神经元的轴突既不需要TRIM46也不需要augmin。我们还表明,在海马神经元而非交感神经元中,当一部分可用的驱动蛋白-1通过药理学方法从细胞器运输转移到微管滑动时,轴突的微管极性模式会被破坏。这些结果共同表明,即使在同一动物中,调节轴突微管极性模式的机制对于不同类型的神经元也不完全相同。