Cason Sydney E, Holzbaur Erika L F
Department of Physiology, University of Pennsylvania.
Neuroscience Graduate Group, University of Pennsylvania.
bioRxiv. 2023 Jan 29:2023.01.28.526044. doi: 10.1101/2023.01.28.526044.
Neuronal autophagosomes, "self-eating" degradative organelles, form at presynaptic sites in the distal axon and are transported to the soma to recycle their cargo. During transit, autophagic vacuoles (AVs) mature through fusion with lysosomes to acquire the enzymes necessary to breakdown their cargo. AV transport is driven primarily by the microtubule motor cytoplasmic dynein in concert with dynactin and a series of activating adaptors that change depending on organelle maturation state. The transport of mature AVs is regulated by the scaffolding proteins JIP3 and JIP4, both of which activate dynein motility in vitro. AV transport is also regulated by ARF6 in a GTP-dependent fashion. While GTP-bound ARF6 promotes the formation of the JIP3/4-dynein-dynactin complex, RAB10 competes with the activity of this complex by increasing kinesin recruitment to axonal AVs and lysosomes. These interactions highlight the complex coordination of motors regulating organelle transport in neurons.
神经元自噬体,即“自我吞噬”的降解细胞器,在轴突远端的突触前位点形成,并被运输到胞体以循环利用其内容物。在运输过程中,自噬泡(AVs)通过与溶酶体融合而成熟,以获得分解其内容物所需的酶。AV运输主要由微管动力蛋白胞质动力蛋白与动力蛋白激活蛋白以及一系列根据细胞器成熟状态而变化的激活衔接蛋白协同驱动。成熟AV的运输受支架蛋白JIP3和JIP4调节,这两种蛋白在体外均能激活动力蛋白的运动。AV运输也受ARF6以GTP依赖方式调节。当结合GTP的ARF6促进JIP3/4-动力蛋白-动力蛋白激活蛋白复合物的形成时,RAB10通过增加驱动蛋白向轴突AV和溶酶体的募集来竞争该复合物的活性。这些相互作用突出了调节神经元细胞器运输的动力蛋白的复杂协调作用。