Advanced Science Research Center, The Graduate Center, City University of New York, New York City, NY 10031, USA; Department of Neuroscience and Behavior, Barnard College of Columbia University, New York City, NY 10027, USA.
Advanced Science Research Center, The Graduate Center, City University of New York, New York City, NY 10031, USA; Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109, USA.
Curr Biol. 2020 Jun 22;30(12):2225-2237.e5. doi: 10.1016/j.cub.2020.04.025. Epub 2020 May 7.
Networks of circadian timekeeping in the brain display marked daily changes in neuronal morphology. In Drosophila melanogaster, the striking daily structural remodeling of the dorsal medial termini of the small ventral lateral neurons has long been hypothesized to mediate endogenous circadian timekeeping. To test this model, we have specifically abrogated these sites of daily neuronal remodeling through the reprogramming of neural development and assessed the effects on circadian timekeeping and clock outputs. Remarkably, the loss of these sites has no measurable effects on endogenous circadian timekeeping or on any of the major output functions of the small ventral lateral neurons. Rather, their loss reduces sites of glutamatergic sensory neurotransmission that normally encodes naturalistic time cues from the environment. These results support an alternative model: structural plasticity in critical clock neurons is the basis for proper integration of light and temperature and gates sensory inputs into circadian clock neuron networks.
大脑中的生物钟网络表现出明显的神经元形态的日常变化。在黑腹果蝇中,小腹外侧神经元的背内侧末端惊人的每日结构重塑,长期以来一直被假设为介导内源性生物钟计时。为了检验这一模型,我们通过神经发育的重新编程特异性地消除了这些每日神经元重塑的部位,并评估了对生物钟计时和时钟输出的影响。值得注意的是,这些部位的缺失对内源性生物钟计时或小腹外侧神经元的任何主要输出功能都没有可测量的影响。相反,它们的缺失减少了通常编码环境中自然时间线索的谷氨酸能感觉神经递质传递的部位。这些结果支持了另一种模型:关键时钟神经元中的结构可塑性是正确整合光和温度以及将感觉输入门控到生物钟神经元网络的基础。