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1
CA3 retrieves coherent representations from degraded input: direct evidence for CA3 pattern completion and dentate gyrus pattern separation.CA3 从退化的输入中获取连贯的表示:CA3 模式完成和齿状回模式分离的直接证据。
Neuron. 2014 Jan 22;81(2):416-27. doi: 10.1016/j.neuron.2013.11.017.
2
Distinct determinants of sparse activation during granule cell maturation.颗粒细胞成熟过程中稀疏激活的不同决定因素。
J Neurosci. 2013 Dec 4;33(49):19131-42. doi: 10.1523/JNEUROSCI.2289-13.2013.
3
Adult neurogenesis in the mammalian hippocampus: why the dentate gyrus?哺乳动物海马体中的成人神经发生:齿状回缘何如此?
Learn Mem. 2013 Nov 19;20(12):710-29. doi: 10.1101/lm.026542.112.
4
Parvalbumin interneurons mediate neuronal circuitry-neurogenesis coupling in the adult hippocampus.钙结合蛋白阳性中间神经元介导成年海马神经元回路-神经发生偶联。
Nat Neurosci. 2013 Dec;16(12):1728-30. doi: 10.1038/nn.3572. Epub 2013 Nov 10.
5
Morpho-physiological criteria divide dentate gyrus interneurons into classes.形态生理标准将齿状回中间神经元分为几类。
Hippocampus. 2014 Feb;24(2):189-203. doi: 10.1002/hipo.22214.
6
Molecular layer perforant path-associated cells contribute to feed-forward inhibition in the adult dentate gyrus.分子层穿通纤维相关细胞有助于成年齿状回的前馈抑制。
Proc Natl Acad Sci U S A. 2013 May 28;110(22):9106-11. doi: 10.1073/pnas.1306912110. Epub 2013 May 13.
7
Neurogenesis in the dentate gyrus: carrying the message or dictating the tone.齿状回中的神经发生:传递信息还是主导基调。
Front Neurosci. 2013 Apr 4;7:50. doi: 10.3389/fnins.2013.00050. eCollection 2013.
8
GABA depolarization is required for experience-dependent synapse unsilencing in adult-born neurons.GABA 去极化是成年神经元中经验依赖性突触去抑制所必需的。
J Neurosci. 2013 Apr 10;33(15):6614-22. doi: 10.1523/JNEUROSCI.0781-13.2013.
9
Retrograde monosynaptic tracing reveals the temporal evolution of inputs onto new neurons in the adult dentate gyrus and olfactory bulb.逆行单突触追踪揭示了成年齿状回和嗅球中新神经元的传入的时间演变。
Proc Natl Acad Sci U S A. 2013 Mar 19;110(12):E1152-61. doi: 10.1073/pnas.1218991110. Epub 2013 Mar 4.
10
Hilar mossy cell degeneration causes transient dentate granule cell hyperexcitability and impaired pattern separation.海拉氏苔藓样细胞变性导致暂时的齿状回颗粒细胞过度兴奋和模式分离受损。
Neuron. 2012 Dec 20;76(6):1189-200. doi: 10.1016/j.neuron.2012.10.036.

在成年新生颗粒细胞整合的关键期内,向反馈抑制的延迟耦合。

Delayed coupling to feedback inhibition during a critical period for the integration of adult-born granule cells.

作者信息

Temprana Silvio G, Mongiat Lucas A, Yang Sung M, Trinchero Mariela F, Alvarez Diego D, Kropff Emilio, Giacomini Damiana, Beltramone Natalia, Lanuza Guillermo M, Schinder Alejandro F

机构信息

Laboratory of Neuronal Plasticity, Leloir Institute-CONICET, Av. Patricias Argentinas 435, Buenos Aires, C1405BWE, Argentina.

Laboratory of Developmental Neurobiology, Leloir Institute-CONICET, Av. Patricias Argentinas 435, Buenos Aires, C1405BWE, Argentina.

出版信息

Neuron. 2015 Jan 7;85(1):116-130. doi: 10.1016/j.neuron.2014.11.023. Epub 2014 Dec 18.

DOI:10.1016/j.neuron.2014.11.023
PMID:25533485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4329739/
Abstract

Developing granule cells (GCs) of the adult dentate gyrus undergo a critical period of enhanced activity and synaptic plasticity before becoming mature. The impact of developing GCs on the activity of preexisting dentate circuits remains unknown. Here we combine optogenetics, acute slice electrophysiology, and in vivo chemogenetics to activate GCs at different stages of maturation to study the recruitment of local target networks. We show that immature (4-week-old) GCs can efficiently drive distal CA3 targets but poorly activate proximal interneurons responsible for feedback inhibition (FBI). As new GCs transition toward maturity, they reliably recruit GABAergic feedback loops that restrict spiking of neighbor GCs, a mechanism that would promote sparse coding. Such inhibitory loop impinges only weakly in new cohorts of young GCs. A computational model reveals that the delayed coupling of new GCs to FBI could be crucial to achieve a fine-grain representation of novel inputs in the dentate gyrus.

摘要

成年齿状回中正在发育的颗粒细胞(GCs)在成熟之前会经历一个活动增强和突触可塑性增强的关键时期。发育中的颗粒细胞对已有齿状回路活动的影响尚不清楚。在这里,我们结合光遗传学、急性脑片电生理学和体内化学遗传学,在不同成熟阶段激活颗粒细胞,以研究局部靶网络的募集情况。我们发现,未成熟(4周龄)的颗粒细胞可以有效地驱动远端CA3靶标,但激活负责反馈抑制(FBI)的近端中间神经元的能力较差。随着新的颗粒细胞向成熟过渡,它们可靠地募集了GABA能反馈回路,这些回路限制了相邻颗粒细胞的放电,这是一种促进稀疏编码的机制。这种抑制性回路对年轻颗粒细胞的新群体影响较弱。一个计算模型表明,新的颗粒细胞与反馈抑制的延迟耦合对于在齿状回中实现新输入的精细表征可能至关重要。