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大鼠神经元烟碱型乙酰胆碱受体α7亚基基因启动子的细胞特异性

Cell specificity of a rat neuronal nicotinic acetylcholine receptor alpha7 subunit gene promoter.

作者信息

Danthi Sanjay, Boyd R Thomas

机构信息

Department of Neuroscience, The Ohio State University College of Medicine and Public Health, Columbus, OH 43210, USA.

出版信息

Neurosci Lett. 2006 May 29;400(1-2):63-8. doi: 10.1016/j.neulet.2006.02.067. Epub 2006 Mar 20.

Abstract

Neuronal nAChRs are pentameric transmembrane proteins which function as ligand-gated ion channels and are composed of multiple alpha and beta subunits. Nine neuronal nAChR alpha subunit genes (alpha2-alpha10) and three nAChR beta subunit genes (beta2-beta4) have been identified. nAChR subtypes are heteromers, composed of various combinations of nAChR subunits or homomers composed of alpha7, alpha8, or alpha9 subunits. nAChR subtypes are widely expressed in the nervous system, yet each subunit has a distinct and unique pattern of expression. This report focuses on the expression of the nAChR alpha7 gene since homomeric nAChRs can be formed from this one subunit, simplifying a study of the expression of a specific nAChR subtype. Alpha7 nAChRs are involved in several important biological activities in addition to synaptic transmission including mediating neurite outgrowth, neuronal development and cell death, and in presynaptic control of neurotransmitter release. Transcriptional regulation of alpha7 gene expression may be important to control the location and timing of these events. We previously isolated a rat alpha7 nAChR promoter and studied expression in PC12 cells. In this study we examined the expression of the alpha7 promoter in PC12, HEK293, L6, SN17 and Neuro-2A cells in order to define elements necessary for cell-specific expression. Elements promoting expression of alpha7 in muscle and fibroblasts were identified. We also demonstrated that several other nAChR genes are also expressed in SN 17 and Neuro-2A cells, supporting use of these cell lines as models to study transcriptional control of nAChR genes.

摘要

神经元烟碱型乙酰胆碱受体(nAChRs)是五聚体跨膜蛋白,作为配体门控离子通道发挥作用,由多个α和β亚基组成。已鉴定出9个神经元nAChRα亚基基因(α2 - α10)和3个nAChRβ亚基基因(β2 - β4)。nAChR亚型是由nAChR亚基的各种组合组成的异聚体,或由α7、α8或α9亚基组成的同聚体。nAChR亚型在神经系统中广泛表达,但每个亚基都有独特的表达模式。本报告重点关注nAChRα7基因的表达,因为同聚体nAChRs可由这一个亚基形成,从而简化了对特定nAChR亚型表达的研究。除了突触传递外,α7 nAChRs还参与多种重要的生物学活动,包括介导神经突生长、神经元发育和细胞死亡,以及对神经递质释放的突触前控制。α7基因表达的转录调控对于控制这些事件的位置和时间可能很重要。我们之前分离了大鼠α7 nAChR启动子并研究了其在PC12细胞中的表达。在本研究中,我们检测了α7启动子在PC12、HEK293、L6、SN17和Neuro - 2A细胞中的表达,以确定细胞特异性表达所需的元件。鉴定出了促进α7在肌肉和成纤维细胞中表达的元件。我们还证明了其他几个nAChR基因也在SN 17和Neuro - 2A细胞中表达,支持将这些细胞系用作研究nAChR基因转录调控的模型。

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