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底物对培养的已鉴定水蛭神经元中钙通道分布的影响。

Influence of substrate on the distribution of calcium channels in identified leech neurons in culture.

作者信息

Ross W N, Aréchiga H, Nicholls J G

机构信息

Department of Physiology, New York Medical College, Valhalla 10595.

出版信息

Proc Natl Acad Sci U S A. 1988 Jun;85(11):4075-8. doi: 10.1073/pnas.85.11.4075.

DOI:10.1073/pnas.85.11.4075
PMID:2453887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC280364/
Abstract

The Retzius neuron from the leech, growing in culture on the plant lectin concanavalin A as substrate, produces broad flat growth cones and thick bundles of processes. The same cell extends fine straight processes with numerous branches when grown on a laminin-like substrate extracted from leech central nervous system extracellular matrix, referred to as "leech laminin extract." Cells growing on these two different substrates also show marked differences in the pattern of Ca2+ entry following evoked impulses, as detected optically by local changes in absorbance of the Ca2+-sensitive dye arsenazo III. Ca2+ enters the soma and initial segment of Retzius cells grown on both substrates. However, detectable Ca2+ entry only occurs into the processes of cells growing on leech laminin but not of those growing on concanavalin A. Optical recordings of changes in membrane potential made with the voltage-sensitive dye RH 155 taken from cells growing on either substrate indicate that a depolarization initiated in the soma spreads to the most distant processes with little or no distortion in amplitude or time course. This implies that all voltage-sensitive Ca2+ channels in the cell membrane are equally activated by depolarizing stimuli. Therefore, the fact that impulses evoke Ca2+ entry into processes of Retzius cells grown on leech laminin extract but not of cells grown on concanavalin A shows that the nature of the growth substrate can affect the number and distribution of their functional Ca2+ channels.

摘要

在以植物凝集素伴刀豆球蛋白A为底物的培养基中生长的水蛭雷丘斯神经元,会产生宽阔扁平的生长锥和粗壮的神经突束。当该细胞在从水蛭中枢神经系统细胞外基质中提取的一种类层粘连蛋白底物(称为“水蛭层粘连蛋白提取物”)上生长时,会伸出带有大量分支的细长直神经突。在这两种不同底物上生长的细胞,在诱发冲动后Ca²⁺内流模式上也表现出显著差异,这是通过对Ca²⁺敏感染料偶氮胂III吸光度的局部变化进行光学检测得到的。Ca²⁺会进入在两种底物上生长的雷丘斯细胞的胞体和起始段。然而,可检测到的Ca²⁺内流仅发生在水蛭层粘连蛋白上生长的细胞的神经突中,而在伴刀豆球蛋白A上生长的细胞则不会。用电压敏感染料RH 155对在任何一种底物上生长的细胞进行膜电位变化的光学记录表明,在胞体引发的去极化会传播到最远的神经突,其幅度或时间进程几乎没有失真。这意味着细胞膜上所有的电压敏感Ca²⁺通道都被去极化刺激同等激活。因此,冲动能使Ca²⁺进入在水蛭层粘连蛋白提取物上生长的雷丘斯细胞的神经突,但不能进入在伴刀豆球蛋白A上生长的细胞,这一事实表明生长底物的性质会影响其功能性Ca²⁺通道的数量和分布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b8f/280364/148137a09089/pnas00263-0425-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b8f/280364/148137a09089/pnas00263-0425-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b8f/280364/148137a09089/pnas00263-0425-a.jpg

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