Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
J Cell Biol. 2012 Feb 20;196(4):407-17. doi: 10.1083/jcb.201106120. Epub 2012 Feb 13.
Autophagy is an essential cellular degradation pathway in neurons; defects in autophagy are sufficient to induce neurodegeneration. In this paper, we investigate autophagosome dynamics in primary dorsal root ganglion neurons. Autophagosome biogenesis occurs distally in a constitutive process at the neurite tip. Autophagosomes initially move bidirectionally and then switch to unidirectional, processive movement toward the cell soma driven by dynein. Autophagosomes copurify with anterograde and retrograde motors, suggesting that the activity of bound kinesin motors is effectively down-regulated to yield robust retrograde motility driven by dynein. Both organelle and soluble cargoes are internalized into autophagosomes, including mitochondria and ubiquitin. As autophagosomes move distally to proximally, they undergo maturation and become increasingly acidified, consistent with the formation of an autolysosomal compartment that may more efficiently degrade cargo. This maturation is accompanied by a switch to bidirectional motility characteristic of lysosomes. Together, autophagosome biogenesis and maturation in primary neurons is a constitutive process that is spatially and temporally regulated along the axon.
自噬是神经元中一种重要的细胞降解途径;自噬缺陷足以诱导神经退行性变。在本文中,我们研究了原代背根神经节神经元中的自噬体动力学。自噬体生物发生在轴突末端的一个组成性过程中远程发生。自噬体最初双向移动,然后在动力蛋白的驱动下切换为单向、连续向细胞体移动。自噬体与正向和反向马达共纯化,表明结合的驱动蛋白马达的活性被有效下调,从而产生由动力蛋白驱动的强大逆行运动。细胞器和可溶性货物都被内化到自噬体中,包括线粒体和泛素。随着自噬体从远端向近端移动,它们经历成熟并变得越来越酸化,与形成自溶酶体隔室一致,这可能更有效地降解货物。这种成熟伴随着向双向运动的转变,这种双向运动是溶酶体的特征。总之,原代神经元中的自噬体生物发生和成熟是一个沿轴突空间和时间调节的组成性过程。