编码持久内部状态的线吸引子需要神经肽信号。

IF 45.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Cell Pub Date : 2024-10-17 Epub Date: 2024-08-26 DOI:10.1016/j.cell.2024.08.015
George Mountoufaris, Aditya Nair, Bin Yang, Dong-Wook Kim, Amit Vinograd, Samuel Kim, Scott W Linderman, David J Anderson
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引用次数: 0

摘要

内部状态是生存行为的驱动力,但人们对它们的神经实现却知之甚少。最近,我们在腹内侧下丘脑(VMH)中发现了一种代表攻击性状态的线性吸引子。线性吸引子可以通过递归连接或神经调节信号来实现,但后者的证据很少。在这里,我们利用基于细胞特异性 CRISPR-Cas9 的基因编辑技术并结合单细胞钙成像,证明神经肽能信号是该系统中线吸引子动态变化的必要条件。在控制攻击的成年 VMH Esr1+ 神经元中同时破坏催产素和血管加压素的受体会减少攻击、降低持续的神经活动并消除线性吸引子动力学,同时只略微降低整体神经活动和性别或行为特异性调谐。这些数据确定了神经肽能信号在实施哺乳动物行为相关的线性吸引子中的必要作用。我们的研究方法将有助于神经科学的机理研究,在生物功能和抽象概念的不同层次之间架起一座桥梁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A line attractor encoding a persistent internal state requires neuropeptide signaling.

A line attractor encoding a persistent internal state requires neuropeptide signaling.

Internal states drive survival behaviors, but their neural implementation is poorly understood. Recently, we identified a line attractor in the ventromedial hypothalamus (VMH) that represents a state of aggressiveness. Line attractors can be implemented by recurrent connectivity or neuromodulatory signaling, but evidence for the latter is scant. Here, we demonstrate that neuropeptidergic signaling is necessary for line attractor dynamics in this system by using cell-type-specific CRISPR-Cas9-based gene editing combined with single-cell calcium imaging. Co-disruption of receptors for oxytocin and vasopressin in adult VMH Esr1+ neurons that control aggression diminished attack, reduced persistent neural activity, and eliminated line attractor dynamics while only slightly reducing overall neural activity and sex- or behavior-specific tuning. These data identify a requisite role for neuropeptidergic signaling in implementing a behaviorally relevant line attractor in mammals. Our approach should facilitate mechanistic studies in neuroscience that bridge different levels of biological function and abstraction.

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来源期刊
Cell
Cell 生物-生化与分子生物学
CiteScore
110.00
自引率
0.80%
发文量
396
审稿时长
2 months
期刊介绍: Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO). The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries. In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.
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