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相关性图谱能够根据大鼠新皮层中的单细胞基因表达谱预测神经元的电特性。

Correlation maps allow neuronal electrical properties to be predicted from single-cell gene expression profiles in rat neocortex.

作者信息

Toledo-Rodriguez Maria, Blumenfeld Barak, Wu Caizhi, Luo Junyi, Attali Bernard, Goodman Philip, Markram Henry

机构信息

Brain and Mind Institute, EPFL, Lausanne 1015, Switzerland.

出版信息

Cereb Cortex. 2004 Dec;14(12):1310-27. doi: 10.1093/cercor/bhh092. Epub 2004 Jun 10.

DOI:10.1093/cercor/bhh092
PMID:15192011
Abstract

The computational power of the neocortex arises from interactions of multiple neurons, which display a wide range of electrical properties. The gene expression profiles underlying this phenotypic diversity are unknown. To explore this relationship, we combined whole-cell electrical recordings with single-cell multiplex RT-PCR of rat (p13-16) neocortical neurons to obtain cDNA libraries of 26 ion channels (including voltage activated potassium channels, Kv1.1/2/4/6, Kvbeta1/2, Kv2.1/2, Kv3.1/2/3/4, Kv4.2/3; sodium/potassium permeable hyperpolarization activated channels, HCN1/2/3/4; the calcium activated potassium channel, SK2; voltage activated calcium channels, Caalpha1A/B/G/I, Cabeta1/3/4), three calcium binding proteins (calbindin, parvalbumin and calretinin) and GAPDH. We found a previously unreported clustering of ion channel genes around the three calcium-binding proteins. We further determined that cells similar in their expression patterns were also similar in their electrical properties. Subsequent regression modeling with statistical resampling yielded a set of coefficients that reliably predicted electrical properties from the expression profile of individual neurons. This is the first report of a consistent relationship between the co-expression of a large profile of ion channel and calcium binding protein genes and the electrical phenotype of individual neocortical neurons.

摘要

新皮质的计算能力源于多个神经元之间的相互作用,这些神经元表现出广泛的电学特性。这种表型多样性背后的基因表达谱尚不清楚。为了探究这种关系,我们将大鼠(p13 - 16)新皮质神经元的全细胞膜片钳电生理记录与单细胞多重逆转录聚合酶链反应相结合,以获得26种离子通道(包括电压门控钾通道,Kv1.1/2/4/6、Kvβ1/2、Kv2.1/2、Kv3.1/2/3/4、Kv4.2/3;钠/钾通透超极化激活通道,HCN1/2/3/4;钙激活钾通道,SK2;电压门控钙通道,Caα1A/B/G/I、Caβ1/3/4)、三种钙结合蛋白(钙结合蛋白、小白蛋白和钙视网膜蛋白)以及甘油醛-3-磷酸脱氢酶(GAPDH)的互补DNA文库。我们发现了离子通道基因在三种钙结合蛋白周围存在先前未报道的聚类现象。我们进一步确定,表达模式相似的细胞在电学特性上也相似。随后通过统计重采样进行的回归建模得出了一组系数,这些系数能够根据单个神经元的表达谱可靠地预测其电学特性。这是首次报道大量离子通道和钙结合蛋白基因的共表达与单个新皮质神经元的电生理表型之间存在一致的关系。

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