海马颗粒细胞在培养条件下下调gaba能表型并使其活性依赖性再诱导失活。

IF 1.6 4区 医学 Q4 NEUROSCIENCES
Synapse Pub Date : 2025-03-01 DOI:10.1002/syn.70012
Gisela Gómez-Lira, Héctor Castro, Arturo Reyes-Vaca, Rafael Gutiérrez
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引用次数: 0

摘要

海马颗粒细胞在发育过程中表达gaba能和谷氨酸能表型标记;因此,它们共同释放GABA和谷氨酸。在成人中,gaba能表型被关闭;然而,增加的兴奋性上调GABA能表型,因此,颗粒细胞共同释放谷氨酸和GABA。先前的研究表明,成年大鼠制备的分离颗粒细胞短期培养(24小时),不表达GAD或VGAT,当暴露于kainic酸和BDNF时,可以表达这些标记。我们在这里测试相同的操作是否能使颗粒细胞在细胞连接的长期培养中共同释放谷氨酸和GABA。有趣的是,我们发现长期培养的细胞不能表达gabaergy表型,尽管在发育过程中呈现出这种表型,并且通过配对记录,我们证实颗粒细胞只释放谷氨酸。长期隔离的颗粒细胞的发育可能剥夺了正常细胞环境提供的使表型改变的必要信号。通过比较它们在原位和培养条件下的发育情况,应该进一步探索可能导致这种情况的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hippocampal Granule Cells Downregulate Their GABAergic Phenotype and Deactivate Its Activity-Dependent Reinduction in Culture Conditions.

Hippocampal granule cells express GABAergic and glutamatergic phenotype markers during development; hence, they corelease GABA and glutamate. In the adult, the GABAergic phenotype is switched off; however, increased excitability upregulates the GABAergic phenotype and thus, granule cells corelease glutamate and GABA. Previous work shows that short-term cultures (24 h) of dissociated granule cells prepared from adult rats, which do not express GAD or VGAT, can express these markers when exposed to kainic acid and BDNF. We here test whether the same manipulation enables granule cells to corelease glutamate and GABA in long-term cultures where cells are connected. Interestingly, we find that long-term cultured cells are not able to express the GABAergic phenotype despite presenting it during their development, and with paired recordings, we confirm that granule cells only release glutamate. The development of granule cells in long-term isolation likely deprives them of essential signaling that a normal cellular milieu provides to enable phenotypic change. The molecular mechanisms that could underlie this should be further explored by comparing their development in situ and in cultured conditions.

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来源期刊
Synapse
Synapse 医学-神经科学
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
4-8 weeks
期刊介绍: SYNAPSE publishes articles concerned with all aspects of synaptic structure and function. This includes neurotransmitters, neuropeptides, neuromodulators, receptors, gap junctions, metabolism, plasticity, circuitry, mathematical modeling, ion channels, patch recording, single unit recording, development, behavior, pathology, toxicology, etc.
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