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使用升高的细胞外钾研究神经元去极化依赖过程的优缺点。

Merits and Limitations of Studying Neuronal Depolarization-Dependent Processes Using Elevated External Potassium.

机构信息

Department of Molecular and Cell Biology, School of Natural Sciences, University of California, Merced, United States.

出版信息

ASN Neuro. 2020 Jan-Dec;12:1759091420974807. doi: 10.1177/1759091420974807.


DOI:10.1177/1759091420974807
PMID:33256465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7711227/
Abstract

Elevated extracellular potassium chloride is widely used to achieve membrane depolarization of cultured neurons. This technique has illuminated mechanisms of calcium influx through L-type voltage sensitive calcium channels, activity-regulated signaling, downstream transcriptional events, and many other intracellular responses to depolarization. However, there is enormous variability in these treatments, including durations from seconds to days and concentrations from 3mM to 150 mM KCl. Differential effects of these variable protocols on neuronal activity and transcriptional programs are underexplored. Furthermore, potassium chloride treatments are criticized for being poor representatives of phenomena and are questioned for their effects on cell viability. In this review, we discuss the intracellular consequences of elevated extracellular potassium chloride treatment , the variability of such treatments in the literature, the strengths and limitations of this tool, and relevance of these studies to brain functions and dysfunctions.

摘要

细胞外钾离子浓度升高被广泛用于实现培养神经元的膜去极化。这项技术阐明了通过 L 型电压敏感钙通道、活性调节信号、下游转录事件以及其他许多对去极化的细胞内反应的钙离子内流机制。然而,这些处理方法存在着巨大的差异,包括持续时间从几秒钟到几天,以及浓度从 3mM 到 150mM KCl。这些可变方案对神经元活性和转录程序的不同影响尚未得到充分探索。此外,氯化钾处理被批评为对现象的代表性很差,并因其对细胞活力的影响而受到质疑。在这篇综述中,我们讨论了细胞外钾离子浓度升高处理的细胞内后果,文献中这种处理方法的可变性,以及该工具的优缺点,以及这些研究与大脑功能和功能障碍的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f04d/7711227/df9fff0a9d8a/10.1177_1759091420974807-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f04d/7711227/4f924b3bf3e8/10.1177_1759091420974807-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f04d/7711227/df9fff0a9d8a/10.1177_1759091420974807-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f04d/7711227/4f924b3bf3e8/10.1177_1759091420974807-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f04d/7711227/df9fff0a9d8a/10.1177_1759091420974807-fig2.jpg

相似文献

[1]
Merits and Limitations of Studying Neuronal Depolarization-Dependent Processes Using Elevated External Potassium.

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本文引用的文献

[1]
Mild membrane depolarization in neurons induces immediate early gene transcription and acutely subdues responses to a successive stimulus.

J Biol Chem. 2022-9

[2]
Simultaneous calcium recordings of hippocampal CA1 and primary motor cortex M1 and their relations to behavioral activities in freely moving epileptic mice.

Exp Brain Res. 2020-6

[3]
Mechanisms that communicate features of neuronal activity to the genome.

Curr Opin Neurobiol. 2020-5-13

[4]
Certain ortho-hydroxylated brominated ethers are promiscuous kinase inhibitors that impair neuronal signaling and neurodevelopmental processes.

J Biol Chem. 2020-3-30

[5]
Background calcium induced by subthreshold depolarization modifies homosynaptic facilitation at a synapse in Aplysia.

Sci Rep. 2020-1-17

[6]
Segregation of seizures and spreading depolarization across cortical layers.

Epilepsia. 2019-11-21

[7]
The Paroxysmal Depolarization Shift: Reconsidering Its Role in Epilepsy, Epileptogenesis and Beyond.

Int J Mol Sci. 2019-1-29

[8]
Bridging Synaptic and Epigenetic Maintenance Mechanisms of the Engram.

Front Mol Neurosci. 2018-10-5

[9]
Stimulation-induced structural changes at the nucleus, endoplasmic reticulum and mitochondria of hippocampal neurons.

Mol Brain. 2018-7-27

[10]
Calmodulin shuttling mediates cytonuclear signaling to trigger experience-dependent transcription and memory.

Nat Commun. 2018-6-22

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