Department of Biochemistry, Fukushima Medical University School of Medicine, Fukushima, Japan.
Division of Cell Physiology, Department of Physiology and Cell Biology, Graduate School of Medicine, Kobe University, Kobe, Japan.
Commun Biol. 2024 Oct 11;7(1):1305. doi: 10.1038/s42003-024-07023-6.
Lysosomes, crucial cellular organelles, undergo bidirectional transport along microtubules, mediated by motor proteins such as cytoplasmic dynein-1 (dynein) and various kinesins. While the kinesin-3 family member KIF1C is established in mediating anterograde vesicle transport, its role in lysosomal transport remains unclear. Our study reveals that KIF1C unexpectedly supports the retrograde transport of lysosomes, driven by dynein, and contributes to their perinuclear localization. Notably, while KIF1C facilitates this perinuclear positioning, its motor activity is not required and, instead, exerts an inhibitory effect on this process. Mechanistically, KIF1C facilitates this process by interacting with the dynein-activating adaptor Hook3, which associates with the lysosome-anchored protein RUFY3. This regulatory mechanism is critical for the efficient degradation of cargo in autophagic and endocytic pathways. Our findings identify an unconventional, non-motor role for KIF1C in activating dynein-driven lysosomal transport, expanding our understanding of its functional diversity in cellular trafficking.
溶酶体是重要的细胞细胞器,沿着微管进行双向运输,这一过程由细胞质动力蛋白-1(dynein)和各种驱动蛋白等马达蛋白介导。虽然驱动蛋白-3 家族成员 KIF1C 已被确定在介导正向囊泡运输中发挥作用,但它在溶酶体运输中的作用尚不清楚。我们的研究揭示了 KIF1C 出人意料地支持由 dynein 驱动的溶酶体逆行运输,并有助于溶酶体向核周区域的定位。值得注意的是,虽然 KIF1C 促进了这种核周定位,但它的运动活性并不是必需的,反而对这个过程有抑制作用。从机制上讲,KIF1C 通过与结合在溶酶体上的蛋白 RUFY3 的 dynein 激活衔接蛋白 Hook3 相互作用来促进这个过程。这种调节机制对于自噬和内吞途径中 cargo 的有效降解至关重要。我们的发现确定了 KIF1C 在激活 dynein 驱动的溶酶体运输中的非传统非马达作用,扩展了我们对其在细胞运输中功能多样性的理解。