下行输入到脊髓V1中间神经元的全脑图。

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2025-02-19 Epub Date: 2024-12-23 DOI:10.1016/j.neuron.2024.11.019
Phillip D Chapman, Anand S Kulkarni, Alexandra J Trevisan, Katie Han, Jennifer M Hinton, Paulina Deltuvaite, Lief E Fenno, Charu Ramakrishnan, Mary H Patton, Lindsay A Schwarz, Stanislav S Zakharenko, Karl Deisseroth, Jay B Bikoff
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引用次数: 0

摘要

运动输出是分布在大脑多个区域的神经回路协调活动的结果,这些神经回路通过下行运动通路将信息传递给脊髓。然而,棘上系统针对脊髓运动回路离散组件的组织逻辑仍不清楚。在这里,利用病毒跨突触追踪和连续双光子断层扫描,我们已经生成了单突触输入到脊髓V1中间神经元的全脑图,这是一个主要的抑制群体,参与运动控制。我们确定了26种直接支配V1中间神经元的不同大脑结构,这些结构跨越后脑的髓质和桥脑区域,以及皮层、中脑、小脑和神经调节系统。此外,我们确定了从椎骨上系统到V1Foxp2和V1Pou6f2神经元亚群的广泛但有偏差的输入。总的来说,这些研究揭示了在分子上不同的中间神经元亚群的下行输入中有偏连通性和收敛的因素,并为理解棘上系统如何影响脊髓运动回路提供了解剖学基础。
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A brain-wide map of descending inputs onto spinal V1 interneurons.

Motor output results from the coordinated activity of neural circuits distributed across multiple brain regions that convey information to the spinal cord via descending motor pathways. Yet the organizational logic through which supraspinal systems target discrete components of spinal motor circuits remains unclear. Here, using viral transsynaptic tracing along with serial two-photon tomography, we have generated a whole-brain map of monosynaptic inputs to spinal V1 interneurons, a major inhibitory population involved in motor control. We identified 26 distinct brain structures that directly innervate V1 interneurons, spanning medullary and pontine regions in the hindbrain as well as cortical, midbrain, cerebellar, and neuromodulatory systems. Moreover, we identified broad but biased input from supraspinal systems onto V1Foxp2 and V1Pou6f2 neuronal subsets. Collectively, these studies reveal elements of biased connectivity and convergence in descending inputs to molecularly distinct interneuron subsets and provide an anatomical foundation for understanding how supraspinal systems influence spinal motor circuits.

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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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