KIF1C facilitates retrograde transport of lysosomes through Hook3 and dynein

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.

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Publication Details

Journal
Communications Biology
Published
2024-10-11
DOI
https://doi.org/10.1038/s42003-024-07023-6
Citations
8
Primary Topic
Cellular transport and secretion
Type
article
Field-Weighted Citation Impact
2.61

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article

KIF1C facilitates retrograde transport of lysosomes through Hook3 and dynein

Yasuhiro Minami, Takeshi Saji, Yasushi Okada, Michiru Nishita et al.
8 citations
Communications Biology
Cellular transport and secretion
2.61
article

KIF1C facilitates retrograde transport of lysosomes through Hook3 and dynein

Yasuhiro Minami, Takeshi Saji, Yasushi Okada, Michiru Nishita, Mitsuharu Endo
article en
8 citations

Abstract

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.

Communications BiologyVol. 7(1)
Fukushima Medical University (JP), RIKEN Center for Biosystems Dynamics Research (JP), Kobe University (JP), The University of Tokyo (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science, Core Research for Evolutional Science and Technology
Openalex Percentile: Top 10%
Cellular transport and secretion
2.61
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