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对Kv4.2进行调控可确定海马锥体神经元A电流的一个特定组成部分,该部分依赖于Kv4.2的表达。

Manipulating Kv4.2 identifies a specific component of hippocampal pyramidal neuron A-current that depends upon Kv4.2 expression.

作者信息

Lauver Aaron, Yuan Li-Lian, Jeromin Andreas, Nadin Brian M, Rodríguez José J, Davies Heather A, Stewart Michael G, Wu Gang-Yi, Pfaffinger Paul J

机构信息

Department of Neuroscience, Baylor College of Medicine, Houston, Texas, USA.

出版信息

J Neurochem. 2006 Nov;99(4):1207-23. doi: 10.1111/j.1471-4159.2006.04185.x. Epub 2006 Oct 5.

DOI:10.1111/j.1471-4159.2006.04185.x
PMID:17026528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3583589/
Abstract

The somatodendritic A-current, I(SA), in hippocampal CA1 pyramidal neurons regulates the processing of synaptic inputs and the amplitude of back propagating action potentials into the dendritic tree, as well as the action potential firing properties at the soma. In this study, we have used RNA interference and over-expression to show that expression of the Kv4.2 gene specifically regulates the I(SA) component of A-current in these neurons. In dissociated hippocampal pyramidal neuron cultures, or organotypic cultured CA1 pyramidal neurons, the expression level of Kv4.2 is such that the I(SA) channels are maintained in the population at a peak conductance of approximately 950 pS/pF. Suppression of Kv4.2 transcripts in hippocampal pyramidal neurons using an RNA interference vector suppresses I(SA) current by 60% in 2 days, similar to the effect of expressing dominant-negative Kv4 channel constructs. Increasing the expression of Kv4.2 in these neurons increases the level of I(SA) to 170% of the normal set point without altering the biophysical properties. Our results establish a specific role for native Kv4.2 transcripts in forming and maintaining I(SA) current at characteristic levels in hippocampal pyramidal neurons.

摘要

海马体CA1区锥体神经元中的树突体A电流(I(SA))可调节突触输入的处理过程、向树突传播的动作电位的幅度以及胞体处的动作电位发放特性。在本研究中,我们利用RNA干扰和过表达技术表明,Kv4.2基因的表达特异性地调节这些神经元中A电流的I(SA)成分。在解离的海马体锥体神经元培养物或器官型培养的CA1区锥体神经元中,Kv4.2的表达水平可使I(SA)通道在群体中维持在约950 pS/pF的峰值电导。使用RNA干扰载体抑制海马体锥体神经元中的Kv4.2转录本,可在2天内使I(SA)电流抑制60%,这与表达显性负性Kv4通道构建体的效果相似。增加这些神经元中Kv4.2的表达可使I(SA)水平增加至正常设定点的170%,而不改变其生物物理特性。我们的结果确定了天然Kv4.2转录本在海马体锥体神经元中以特征水平形成和维持I(SA)电流方面的特定作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/6f23d2862ada/nihms-421836-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/f7c15fe4c840/nihms-421836-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/14f4684ee335/nihms-421836-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/77cdea28e660/nihms-421836-f0003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/c01213e09f2e/nihms-421836-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/02fe4905c29e/nihms-421836-f0006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/ca9dd5220f5a/nihms-421836-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/602a68d76351/nihms-421836-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/6f23d2862ada/nihms-421836-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/f7c15fe4c840/nihms-421836-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/14f4684ee335/nihms-421836-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/77cdea28e660/nihms-421836-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/ad294ef48afc/nihms-421836-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/c01213e09f2e/nihms-421836-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/02fe4905c29e/nihms-421836-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/c45d14e4491d/nihms-421836-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/ca9dd5220f5a/nihms-421836-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/602a68d76351/nihms-421836-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b9/3583589/6f23d2862ada/nihms-421836-f0010.jpg

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Circ Res. 2005 Dec 9;97(12):1342-50. doi: 10.1161/01.RES.0000196559.63223.aa. Epub 2005 Nov 17.
2
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3
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J Physiol. 2005 Nov 1;568(Pt 3):767-88. doi: 10.1113/jphysiol.2005.087858. Epub 2005 Aug 25.
4
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5
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J Physiol. 2005 Aug 1;566(Pt 3):689-715. doi: 10.1113/jphysiol.2005.086835. Epub 2005 May 12.
6
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7
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8
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9
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10
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