Activity-dependent synaptic competition and dendrite pruning in developing mitral cells.

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Frontiers in Neural Circuits Pub Date : 2025-01-27 eCollection Date: 2025-01-01 DOI:10.3389/fncir.2025.1541926
Takeshi Imai
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引用次数: 0

Abstract

During the early postnatal period, neurons in sensory circuits dynamically remodel their connectivity to acquire discrete receptive fields. Neuronal activity is thought to play a central role in circuit remodeling during this period: Neuronal activity stabilizes some synaptic connections while eliminating others. Synaptic competition plays a central role in the binary choice between stabilization and elimination. While activity-dependent "punishment signals" propagating from winner to loser synapses have been hypothesized to drive synapse elimination, their exact nature has remained elusive. In this review, I summarize recent studies in mouse mitral cells that explain how only one dendrite is stabilized while others are eliminated, based on early postnatal spontaneous activity in the olfactory bulb. I discuss how the hypothetical punishment signals act on loser but not winner dendrites to establish only one primary dendrite per mitral cell, the anatomical basis for the odorant receptor-specific parallel information processing in the olfactory bulb.

在出生后早期,感觉回路中的神经元会动态重塑其连接,以获得离散的感受野。在这一时期,神经元活动被认为在电路重塑中起着核心作用:神经元活动会稳定一些突触连接,同时消除另一些突触连接。在稳定与消除的二元选择中,突触竞争起着核心作用。虽然有人假设从赢家到输家的突触传播的依赖于活动的 "惩罚信号 "驱动了突触的消除,但它们的确切性质仍然难以捉摸。在这篇综述中,我总结了最近在小鼠有丝分裂细胞中进行的研究,这些研究基于出生后早期嗅球的自发活动,解释了如何只有一个树突被稳定,而其他树突被消除。我将讨论假定的惩罚信号是如何作用于输家树突而非赢家树突,从而使每个有丝分裂细胞只建立一个初级树突,这就是嗅球中气味受体特异性平行信息处理的解剖学基础。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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