Activity-dependent dendrite patterning in the postnatal barrel cortex

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Naoki Nakagawa, Takuji Iwasato
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Abstract

For neural circuit construction in the brain, coarse neuronal connections are assembled prenatally following genetic programs, being reorganized postnatally by activity-dependent mechanisms to implement area-specific computational functions. Activity-dependent dendrite patterning is a critical component of neural circuit reorganization, whereby individual neurons rearrange and optimize their presynaptic partners. In the rodent primary somatosensory cortex (barrel cortex), driven by thalamocortical inputs, layer 4 (L4) excitatory neurons extensively remodel their basal dendrites at neonatal stages to ensure specific responses of barrels to the corresponding individual whiskers. This feature of barrel cortex L4 neurons makes them an excellent model, significantly contributing to unveiling the activity-dependent nature of dendrite patterning and circuit reorganization. In this review, we summarize recent advances in our understanding of the activity-dependent mechanisms underlying dendrite patterning. Our focus lays on the mechanisms revealed by in vivo time-lapse imaging, and the role of activity-dependent Golgi apparatus polarity regulation in dendrite patterning. We also discuss the type of neuronal activity that could contribute to dendrite patterning and hence connectivity.
后天桶状皮层中依赖活动的树突模式化
在大脑中构建神经回路时,粗大的神经元连接在出生前按照遗传程序组装,出生后通过活动依赖机制重组,以实现特定区域的计算功能。依赖于活动的树突形态是神经回路重组的一个关键组成部分,单个神经元在此过程中重新排列并优化其突触前伙伴。在啮齿动物初级体感皮层(桶状皮层)中,丘脑皮层输入驱动的第 4 层(L4)兴奋神经元在新生儿阶段广泛重塑其基底树突,以确保桶状皮层对相应的单个胡须做出特异性反应。桶状皮层 L4 神经元的这一特征使其成为一个极好的模型,为揭示树突形态和电路重组的活动依赖性做出了重要贡献。在这篇综述中,我们总结了最近在理解树突形态的活动依赖机制方面取得的进展。我们的重点是活体延时成像所揭示的机制,以及活动依赖性高尔基体极性调控在树突形态形成中的作用。我们还讨论了神经元活动的类型,这些活动可能有助于树突形态的形成,从而促进连接。
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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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