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猫视觉皮层中一类与活动相关的神经元细胞表面硫酸软骨素蛋白聚糖

A family of activity-dependent neuronal cell-surface chondroitin sulfate proteoglycans in cat visual cortex.

作者信息

Lander C, Kind P, Maleski M, Hockfield S

机构信息

Section of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8001, USA.

出版信息

J Neurosci. 1997 Mar 15;17(6):1928-39. doi: 10.1523/JNEUROSCI.17-06-01928.1997.

Abstract

Monoclonal antibody Cat-301 recognizes a chondroitin sulfate proteoglycan (CSPG) expressed on the extracellular surface of cell bodies and proximal dendrites of specific subsets of neurons in many areas of the mammalian CNS, including the cat visual cortex. The Cat-301 CSPG is first detected at the close of the critical period in development, a period during which the pattern of neuronal activity determines the mature synaptic circuitry and neuronal phenotype. In the cat visual cortex, dark-rearing from birth prolongs the duration of the critical period and attenuates the expression of the Cat-301 antigen, implicating the Cat-301 CSPG in the cellular mechanisms that terminate the period of synaptic plasticity. Because the Cat-301 antigen is expressed on only a limited subset of neurons, we have further examined the molecular heterogeneity among neuronal cell-surface CSPGs and have asked (1) whether other neuronal subsets carry distinct CSPGs and (2) whether the activity-dependent expression of the Cat-301 CSPG is a property generalizable to related cell-surface CSPGs. Here, we report two new monoclonal antibodies, Cat-315 and Cat-316, which together with Cat-301 define a family of at least seven related yet distinct CSPGs. These three antibodies define nonidentical subsets of neurons in the cat visual cortex. The expression of normal levels of these CSPGs is reduced by dark-rearing. Together, these data show that the family of cell-surface CSPGs is molecularly diverse, that different sets of neurons express distinct complements of cell-surface antigens, and that the regulation of CSPG expression by activity may be a general feature of neuronal cell-surface CSPGs.

摘要

单克隆抗体Cat-301识别一种硫酸软骨素蛋白聚糖(CSPG),该蛋白聚糖表达于哺乳动物中枢神经系统许多区域(包括猫视觉皮层)特定神经元亚群的细胞体和近端树突的细胞外表面。Cat-301 CSPG在发育关键期结束时首次被检测到,在此期间,神经元活动模式决定了成熟的突触回路和神经元表型。在猫视觉皮层中,出生后进行暗饲养会延长关键期的持续时间,并减弱Cat-301抗原的表达,这表明Cat-301 CSPG参与了终止突触可塑性时期的细胞机制。由于Cat-301抗原仅在有限的神经元亚群上表达,我们进一步研究了神经元细胞表面CSPG之间的分子异质性,并提出了以下问题:(1)其他神经元亚群是否携带不同的CSPG;(2)Cat-301 CSPG的活性依赖性表达是否是相关细胞表面CSPG的普遍特性。在此,我们报告了两种新的单克隆抗体Cat-315和Cat-316,它们与Cat-301一起定义了一个至少由七种相关但不同的CSPG组成的家族。这三种抗体定义了猫视觉皮层中不同的神经元亚群。暗饲养会降低这些CSPG正常水平的表达。这些数据共同表明,细胞表面CSPG家族在分子上具有多样性,不同的神经元组表达不同的细胞表面抗原组合,并且活性对CSPG表达的调节可能是神经元细胞表面CSPG的一个普遍特征。

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