Xu Ye, Zhang Lin, Liu Yan, Topalidou Irini, Hassinan Cera, Ailion Michael, Zhao Zhenqiang, Wang Tan, Chen Zhibin, Bai Jihong
Department of Clinical Medicine, Nanjing Medical University, Nanjing 211166, P. R. China.
Basic Sciences Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N., Seattle, WA 98109, USA.
iScience. 2021 Mar 1;24(4):102247. doi: 10.1016/j.isci.2021.102247. eCollection 2021 Apr 23.
Animals require robust yet flexible programs to support locomotion. Here we report a pathway that connects the D1-like dopamine receptor DOP-1 with a sleep mechanism to modulate swimming in . We show that DOP-1 plays a negative role in sustaining swimming behavior. By contrast, a pathway through the D2-like dopamine receptor DOP-3 negatively regulates the initiation of swimming, but its impact fades quickly over a few minutes. We find that DOP-1 and the GPCR kinase (G-protein-coupled receptor kinase-2) function in the sleep interneuron RIS, where DOP-1 modulates the secretion of a sleep neuropeptide FLP-11. We further show that DOP-1 and FLP-11 act in the same pathway to modulate swimming. Together, these results delineate a functional connection between a dopamine receptor and a sleep program to regulate swimming in . The temporal transition between DOP-3 and DOP-1 pathways highlights the dynamic nature of neuromodulation for rhythmic movements that persist over time.
动物需要强大而灵活的程序来支持运动。在此,我们报告了一条将D1样多巴胺受体DOP-1与一种睡眠机制相连接以调节[具体动物]游泳的途径。我们表明,DOP-1在维持游泳行为中起负面作用。相比之下,一条通过D2样多巴胺受体DOP-3的途径对游泳的起始起负调节作用,但其影响在几分钟内迅速消退。我们发现,DOP-1和GPCR激酶(G蛋白偶联受体激酶-2)在睡眠中间神经元RIS中发挥作用,在那里DOP-1调节睡眠神经肽FLP-11的分泌。我们进一步表明,DOP-1和FLP-11在同一途径中发挥作用以调节游泳。总之,这些结果描绘了多巴胺受体与调节[具体动物]游泳的睡眠程序之间的功能联系。DOP-3和DOP-1途径之间的时间转换突出了随着时间持续的节律性运动的神经调节的动态性质。