Singh Kamaldeep, Das Semanti, Sutradhar Sabyasachi, Howard Jonathon, Ray Krishanu
Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai - 400005, India.
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT - 06520, United States.
bioRxiv. 2024 Jun 5:2024.04.24.590898. doi: 10.1101/2024.04.24.590898.
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 and humans, respectively. However, how the transport of Rab4-associated vesicles is regulated in neurons remains unknown. Using time-lapse imaging of 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.
Rab4 GTP酶组织内体分选,这对于维持再循环和降解途径之间的平衡至关重要。Rab4定位于许多货物,其在神经元中的运输对于调节神经传递和神经元健康至关重要。此外,中枢神经系统中Rab4水平升高分别与果蝇和人类的突触萎缩和神经退行性变有关。然而,Rab4相关囊泡在神经元中的运输如何被调节仍然未知。利用果蝇幼虫的延时成像,我们发现通过Dilp2和dInR激活胰岛素信号会增加轴突中Rab4囊泡的顺行速度、运行长度和通量。在分子层面,我们发现神经元胰岛素信号的激活会进一步激活Vps34, 提高Rab4相关囊泡上PI(3)P的水平,招募Klp98A(一种PI(3)P结合的驱动蛋白-3马达蛋白)并激活其顺行运输。总之,这些观察结果阐明了胰岛素信号在调节轴突运输和突触稳态中的作用。