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树突棘动力学受单眼剥夺和细胞外基质降解的调节。

Dendritic spine dynamics are regulated by monocular deprivation and extracellular matrix degradation.

作者信息

Oray Serkan, Majewska Ania, Sur Mriganka

机构信息

Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

Neuron. 2004 Dec 16;44(6):1021-30. doi: 10.1016/j.neuron.2004.12.001.


DOI:10.1016/j.neuron.2004.12.001
PMID:15603744
Abstract

The mammalian primary visual cortex (V1) is especially susceptible to changes in visual input over a well-defined critical period, during which closing one eye leads to a loss of responsiveness of neurons to the deprived eye and a shift in response toward the open eye. This functional plasticity can occur rapidly, following even a single day of eye closure, although the structural bases of these changes are unknown. Here, we show that rapid structural changes at the level of dendritic spines occur following brief monocular deprivation. These changes are evident in the supra- and infragranular layers of the binocular zone and can be mimicked by degradation of the extracellular matrix with the tPA/plasmin proteolytic cascade. Further, monocular deprivation occludes a subsequent effect of matrix degradation, suggesting that this mechanism is active in vivo to permit structural remodeling during ocular dominance plasticity.

摘要

哺乳动物的初级视觉皮层(V1)在一个明确的关键期内对视觉输入的变化特别敏感,在此期间,闭上一只眼睛会导致神经元对被剥夺的眼睛的反应性丧失,并使反应向睁开的眼睛转移。即使仅闭眼一天,这种功能可塑性也会迅速出现,尽管这些变化的结构基础尚不清楚。在这里,我们表明,短暂的单眼剥夺后,树突棘水平会发生快速的结构变化。这些变化在双眼区的颗粒上层和颗粒下层很明显,并且可以通过组织型纤溶酶原激活剂(tPA)/纤溶酶蛋白水解级联反应降解细胞外基质来模拟。此外,单眼剥夺会阻断基质降解的后续效应,这表明该机制在体内是活跃的,以允许在眼优势可塑性期间进行结构重塑。

相似文献

[1]
Dendritic spine dynamics are regulated by monocular deprivation and extracellular matrix degradation.

Neuron. 2004-12-16

[2]
Experience-dependent pruning of dendritic spines in visual cortex by tissue plasminogen activator.

Neuron. 2004-12-16

[3]
Swept contrast visual evoked potentials and their plasticity following monocular deprivation in mice.

Vision Res. 2004-12

[4]
Molecular mechanism for loss of visual cortical responsiveness following brief monocular deprivation.

Nat Neurosci. 2003-8

[5]
Tissue plasminogen activator mediates reverse occlusion plasticity in visual cortex.

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[6]
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Neuron. 2004-12-16

[7]
Homeostatic regulation of eye-specific responses in visual cortex during ocular dominance plasticity.

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[8]
Stimulus for rapid ocular dominance plasticity in visual cortex.

J Neurophysiol. 2006-5

[9]
Binocular Disparity Selectivity Weakened after Monocular Deprivation in Mouse V1.

J Neurosci. 2017-7-5

[10]
Involvement of T-type Ca2+ channels in the potentiation of synaptic and visual responses during the critical period in rat visual cortex.

Eur J Neurosci. 2008-8

引用本文的文献

[1]
Comparative Neuroplasticity in Frontal- and Lateral-Eyed Mammals With Induced-Binocular Vision Dysfunction: Insights From Monocular Deprivation Models.

Eur J Neurosci. 2025-7

[2]
Large-scale synaptic dynamics drive the reconstruction of binocular circuits in mouse visual cortex.

Nat Commun. 2025-7-1

[3]
Prey capture learning drives critical period-specific plasticity in mouse binocular visual cortex.

bioRxiv. 2025-1-28

[4]
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Nutrients. 2024-10-22

[5]
Impact of transcranial Direct Current Stimulation on stereoscopic vision and retinal structure in adult amblyopic rodents.

Eye Brain. 2024-10-31

[6]
Microglial Regulation of Sleep and Wakefulness.

Adv Neurobiol. 2024

[7]
Oligodendrocytes and myelin limit neuronal plasticity in visual cortex.

Nature. 2024-9

[8]
Electrophysiology of Dendritic Spines: Information Processing, Dynamic Compartmentalization, and Synaptic Plasticity.

Adv Neurobiol. 2023

[9]
Dynamic structural remodeling of the human visual system prompted by bilateral retinal gene therapy.

Curr Res Neurobiol. 2023-6-4

[10]
Rapid synaptic and gamma rhythm signature of mouse critical period plasticity.

Proc Natl Acad Sci U S A. 2023-1-10

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