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bioRxiv · 10.1101/2024.04.24.590898

Insulin signaling accelerates the anterograde movement of Rab4 vesicles in axons through Klp98a/KIF16B recruitment via Vps34-PI3Kinase

Singh, K.·Das, S.·Sutradhar, S.·Howard, J.·Ray, K.
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Abstract

Rab4 GTPase organizes endosomal sorting essential for maintaining the balance between recycling and degradative pathways. Rab4 localizes to many cargos whose transport in neurons is critical for regulating neurotransmission and neuronal health. Furthermore, elevated Rab4 levels in the CNS are associated with synaptic atrophy and neurodegeneration in Drosophila and humans, respectively. However, how the transport of Rab4-associated vesicles is regulated in neurons remains unknown. Using in vivo time-lapse imaging of Drosophila larvae, we show that activation of insulin signaling via Dilp2 and dInR increases the anterograde velocity, run length, and flux of Rab4 vesicles in the axons. Molecularly, we show that activation of neuronal insulin signaling further activates Vps34, elevates the levels of PI(3)P on Rab4-associated vesicles, recruits Klp98A (a PI(3)P-binding kinesin-3 motor) and activates their anterograde transport. Together, these observations delineate the role of insulin signaling in regulating axonal transport and synaptic homeostasis. HighlightsO_LIDilp2-mediated insulin signaling activates anterograde transport of Rab4 vesicles C_LIO_LIVps34 regulates anterograde velocity, run length and flux of Rab4 vesicles C_LIO_LILocal PI(3)P signaling on Rab4 vesicles regulates their motility in the axons C_LIO_LIPI(3)P production upon acute insulin stimulation recruits Klp98A on Rab4 vesicles C_LI

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Singh, K., Das, S., Sutradhar, S., Howard, J., Ray, K.. 2024-04-24. Insulin signaling accelerates the anterograde movement of Rab4 vesicles in axons through Klp98a/KIF16B recruitment via Vps34-PI3Kinase. https://doi.org/10.1101/2024.04.24.590898

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