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Sensory Deprivation Alters Aggrecan and Perineuronal Net Expression in the Mouse Barrel Cortex

机译:感觉剥夺改变小鼠桶皮质中的Aggrecan和神经周围神经元的净表达。

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摘要

An important role for the neural extracellular matrix in modulating cortical activity-dependent synaptic plasticity has been established by a number of recent studies. However, identification of the critical molecular components of the neural matrix that mediate these processes is far from complete. Of particular interest is the perineuronal net (PN), an extracellular matrix component found surrounding the cell body and proximal neurites of a subset of neurons. Because of the apposition of the PN to synapses and expression of this structure coincident with the close of the critical period, it has been hypothesized that nets could play uniquely important roles in synapse stabilization and maturation. Interestingly, previous work has also shown that expression of PNs is dependent on appropriate sensory stimulation in the visual system. Here, we investigated whether PNs in the mouse barrel cortex are expressed in an activity-dependent manner by manipulating sensory input through whisker trimming. Importantly, this manipulation did not lead to a global loss of PNs but instead led to a specific decrease in PNs, detected with the antibody Cat-315, in layer IV of the barrel cortex. In addition, we identified a key activity-regulated component of PNs is the proteoglycan aggrecan. We also demonstrate that these Cat-315-positive neurons virtually all also express parvalbumin. Together, these data are in support of an important role for aggrecan in the activity-dependent formation of PNs on parvalbumin-expressing cells and suggest a role for expression of these nets in regulating the close of the critical period.
机译:最近的许多研究已经确定了神经细胞外基质在调节皮质活性依赖性突触可塑性中的重要作用。但是,鉴定介导这些过程的神经基质的关键分子成分远未完成。特别感兴趣的是神经周围神经网(PN),这是一种围绕细胞体和神经元子集的近端神经突的细胞外基质成分。由于PN与突触并置且该结构的表达与关键时期的结束相吻合,因此推测网络在突触的稳定和成熟中可以发挥独特的重要作用。有趣的是,以前的工作还表明,PNs的表达取决于视觉系统中适当的感觉刺激。在这里,我们研究了通过操纵晶须修剪来控制感觉输入,是否通过活动依赖的方式表达了小鼠桶状皮质中的PN。重要的是,这种操作并不会导致PN的整体丢失,而是导致了桶状皮质IV层中用Cat-315抗体检测到的PN的特异性降低。此外,我们确定了PNs的关键活性调节成分是蛋白聚糖聚集蛋白聚糖。我们还证明,这些Cat-315阳性神经元实际上也都表达小白蛋白。总之,这些数据支持聚集蛋白聚糖在表达小白蛋白的细胞上依赖于活性的PNs形成中的重要作用,并暗示这些网的表达在调节关键时期的结束中的作用。

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