Most organelles move bidirectionally on microtubule tracks, yet how this opposing movement is regulated by kinesin and dynein remains unclear. Recent work found that ARL8, a known anterograde adaptor linking the lysosome to kinesin, also links lysosomes to the retrograde motor dynein, providing key insight into bidirectional organelle movement in cells.
Regulation of bidirectional lysosome movement
Cellular cargos achieve precise spatial and temporal distribution via bidirectional transport on microtubule tracks. One bidirectionally-transported cargo is the lysosome. Lysosomes (here, the term ‘lysosome’ collectively refers to late endosomes, lysosomes, and endolysosomes) are membrane-enclosed structures crucial for cellular health and energy homeostasis. Lysosomes undergo ‘retrograde’ transport toward microtubule minus-ends at the centrosome via cytoplasmic dynein-1 (dynein here) and ‘anterograde’ transport toward microtubule plus-ends at the cell periphery via kinesin motors. Environmental cues, such as nutrient availability, viral infection, and cellular stress regulate the localization and corresponding functions of lysosomes1. For example, nutrient withdrawal leads to lysosome retrograde transport and perinuclear clustering2. There, lysosomes fuse with autophagosomes, which in turn shuts off lysosome-mediated mTORC1 signaling and activates autophagy. In contrast, the re-introduction of growth factors triggers anterograde lysosome movement toward the cell periphery and re-activates mTORC1 signaling required for protein synthesis and inhibition of autophagy3. Nutrient-driven lysosome positioning is also important for ER remodeling and focal adhesion disassembly at the cell membrane4,5. Thus, bidirectional lysosome movement and distribution are key aspects of cellular adaptation to environmental cues. However, the precise molecular mechanisms linking lysosomes to the anterograde or retrograde transport systems are not fully understood.
ARL8 links lysosomes to kinesin for anterograde transport
The opposite-polarity motors dynein and kinesin often associate with cellular organelles via adaptor proteins that link to a small GTPase of the Rab, Arf, or Arf-like (Arl) families6. GTPases cycle through inactive GDP-bound and active, membrane-associated GTP-bound forms. GTPase “effector” proteins directly bind to GTPases in their membrane-associated, GTP-bound form. These effectors can link GTPases to opposite-polarity motors, resulting in organelle movement. Lysosomes are one prime example where GTPases regulate organelle transport in both the anterograde and retrograde directions. For example, the Rab7 GTPase links lysosomes to dynein-dynactin via the RILP adaptor, and to kinesin via FYCO17,8,9.
Another well-established GTPase that regulates lysosome transport is ARL8. Humans have two ARL8 paralogs, ARL8A and ARL8B, with overlapping functions. ARL8 has been demonstrated to associate with kinesins both directly and indirectly, driving lysosome transport in the anterograde direction (Fig. 1). ARL8 directly recruits kinesin-3 to lysosomes and indirectly associates with kinesin-1 by binding to the adaptor protein SKIP (also known as PLEKHM2)10,11. Recruitment of different kinesins by these distinct mechanisms can then facilitate lysosome transport on microtubules with diverse post-translational modifications12. Though ARL8 has a key role in lysosome transport in the anterograde direction, up until now, ARL8 has not been linked to retrograde lysosome transport.
Two recent studies link ARL8 to dynein-mediated transport
Two recent studies by Keren-Kaplan et al.13 and Kumar et al.14 shed light on how ARL8 also acts as a regulator of lysosome retrograde transport. Keren-Kaplan et al. and Kumar et al. identify the RUN- and FYVE-domain-containing protein RUFY3 as a novel ARL8 effector that links lysosomes to the dynein complex for retrograde transport (Fig. 1). Their findings provide a novel example of how small GTPases such as ARL8 regulate the bidirectional movement of cellular structures by linking opposite-polarity motors to cellular cargo.
In these two studies, RUFY3 was identified as an ARL8 interactor by different experimental techniques. Keren-Kaplan et al. used MitoID, a proteomics approach in which the bait protein, ARL8 in this case, is associated with a promiscuous biotin ligase and targeted to mitochondria. This technique identified the ARL8 ‘interactome’ while reducing non-specific cellular interactions. Concurrently, Kumar et al. performed a yeast-two-hybrid experiment with ARL8B and a human brain tissue cDNA library. Both groups identified RUFY3 as an ARL8 interactor and used co-immunoprecipitation and cellular co-localization assays to confirm that RUFY3 associates with GTP-bound ARL8, suggesting that RUFY3 is an ARL8 effector. In addition, Keren-Kaplan et al. showed using co-immunoprecipitation and co-localization studies that RUFY4, but not other members of the RUFY family, can also associate with ARL8. The ARL8-interaction region within RUFY3 was mapped to its coiled-coil (CC2) and FYVE domains. Kumar and colleagues further mapped this interaction to residues R462/K465 and showed using purified proteins that the interaction between RUFY3 and ARL8 is direct, confirming RUFY3 as a novel ARL8 effector.
Multiple studies have shown that ARL8 is critical for kinesin-mediated lysosome movement toward the cell periphery (reviewed in ref. 15). However, overexpression of RUFY3 or RUFY4 (Keren-Kaplan et al.) or co-overexpression of RUFY3 and ARL8 (Kumar et al.) led to a clustering of lysosomes at the nucleus, indicating retrograde, or dynein-mediated, lysosome transport. Therefore, both groups tested if RUFY proteins associate with components of the dynein complex. To achieve processive motility, dynein requires association with the protein complex dynactin and an activating adaptor protein that also links the complex to cargos16,17,18,19. Keren-Kaplan et al. showed that RUFY3 and RUFY4 associate with dynein-dynactin complex components via immunoprecipitation, while Kumar et al. performed affinity purification mass spectrometry of GST-RUFY3 in HEK293T cell lysates and identified dynein and dynactin subunits.
In follow-up experiments, both groups sought to determine how RUFY proteins mediate the association of ARL8 with dynein-dynactin. Keren-Kaplan et al. found that RUFY3 directly interacted with the C-terminal region of the dynein subunit DLIC1, a mode of interaction similar to numerous dynein activating adaptors20. On the other hand, experiments by Kumar et al. demonstrate that RUFY3 may indirectly associate with dynein. Mass spectrometry of RUFY3 identified the proposed dynein activating adaptor JIP4, and JIP4 was required for RUFY3-mediated clustering of lysosomes at the nucleus. Collectively, these data show that RUFY proteins link ARL8-marked lysosomes to the dynein complex either directly or via a JIP4 adaptor.
Finally, both groups tested the contribution of RUFY3-dependent lysosome movement to changes in the cellular environment. During nutrient depletion, the cytoplasmic pH increases, and lysosomes move in the retrograde direction to eventually accumulate at the perinuclear region2. Keren-Kaplan et al. found that shifting the cytoplasm to a higher pH in RUFY3-depleted cells led to a partial reduction in lysosome perinuclear clustering. Similarly, Kumar et al. showed that RUFY3 was required for lysosome repositioning following nutrient depletion. Therefore, the cellular environment can influence the directionality of lysosome transport.
Bidirectional transport regulation occurs at multiple levels
This work and the work of others have elucidated the multiple layers of regulation that act on bidirectional transport at the level of the organelle, the GTPase, the effector, or the motors. At the organelle level, different GTPases can be recruited to the lysosome via different mechanisms. For example, Rab7 attaches to membranes via carboxy-terminal prenyl groups, and this process is tightly controlled by Rab7 binding proteins21. ARL8 lacks the carboxy-terminal residues required for prenylation and instead requires acetylation in its amino-terminal region, as well as association with the BORC complex12,22. Therefore, the amount or type of each GTPase and/or regulatory proteins present on a specific cargo, as well as their rate of GTP hydrolysis could define organelle movement at a broad level.
At the GTPase level, a single GTPase is capable of recruiting multiple different effectors. The ARL8 GTPase can directly recruit kinesin-3, indirectly recruit kinesin-1 via SKIP, or recruit dynein-dynactin via RUFY3 or RUFY4, promoting movement on distinct microtubule tracks or in different directions11,12,13,14. Future work will unravel if these effectors compete for ARL8 binding and what factors impact effector binding.
At the effector level, distinct effectors may recruit the same motor by different mechanisms. The ARL8 effector RUFY3 may directly recruit dynein-dynactin via an interaction with the DLIC, or indirectly via JIP4. Given that dynein requires an association with dynactin and activating adaptor to achieve motility, it remains to be determined if RUFY3 and/or JIP4 are sufficient to activate dynein for motility in addition to linking it to lysosomes. A recent preprint shows the recruitment of tandem activating adaptors to dynein-dynactin, raising the possibility of a potential mechanism where RUFY3 and JIP4 could engage the dynein complex at the same time or utilize another dynein activating adaptor for dynein-mediated motility23. It is possible that recruiting or activating dynein-dynactin by these different mechanisms may result in retrograde movement that differs in speed, run length, or other characteristics.
Finally, at the motor level, different motors may compete for microtubule engagement. Cargos are likely bound by many motors at once. Opposite-polarity motors may engage in a ‘tug-of-war’ with each other, resulting in cargo movement in the direction of the ‘winning’ set of motors. The number of motors can also influence the run length or speed of moving lysosomes, providing an additional level of regulation. It is also possible that the cellular environment, and factors like nutrient depletion, may influence transport regulation at these different levels. Clearly, there are multiple layers of regulation that fine-tune the transport of cargo under different cellular circumstances. Lysosomes will continue to present an ideal test case for understanding the diverse aspects of bidirectional cargo transport in different environmental contexts.
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The authors declare no competing interests.
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Kendrick, A.A., Christensen, J.R. Bidirectional lysosome transport: a balancing act between ARL8 effectors. Nat Commun 13, 5261 (2022). https://doi.org/10.1038/s41467-022-32965-y