大鼠背根神经节中的缝隙连接蛋白 Connexin-43

Q4 Biochemistry, Genetics and Molecular Biology Cell and Tissue Biology Pub Date : 2024-04-15 DOI:10.1134/s1990519x23700049
E. A. Kolos, D. E. Korzhevsky
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引用次数: 0

摘要

摘要 该研究旨在调查大鼠背根神经节(DRG)细胞中缝隙连接蛋白 connexin-43 (Cx43) 在出生后不同阶段的分布和定位动态,以评估细胞间相互作用与年龄相关变化的形态学迹象。这项研究采用免疫组化方法在 4 个月和 18 个月大的 Wistar 大鼠身上进行。使用谷氨酰胺合成酶抗体检测神经胶质细胞,使用 Iba-1 标记检测巨噬细胞。已经证实,含连接蛋白-43 的结构主要存在于幼年和老龄动物的卫星神经胶质细胞中。在所研究的年龄组中,感觉神经元和 DRG 巨噬细胞都不含连接蛋白-43。在分析大鼠背根神经节细胞间联系与年龄有关的变化时,发现富含连接蛋白-43 的区域随着年龄的增长变得越来越多,这些区域与确保背根神经节卫星神经胶质细胞新陈代谢相互作用的蛋白通道斑块相对应。这一事实可能表明,在大鼠衰老过程中,感觉神经节中神经胶质细胞之间的相互作用被激活了。
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Gap Junction Protein Connexin-43 in a Rat Dorsal Root Ganglion

Abstract

The study aimed at investigating the dynamics of the distribution and localization of the gap junction protein connexin-43 (Cx43) in rat dorsal root ganglion (DRG) cells at different stages of postnatal ontogenesis to assess morphological signs of age-related changes in intercellular interactions. The work was performed on Wistar rats aged 4 and 18 months using immunohistochemical methods. Glial cells were detected using antibodies to glutamine synthetase, and Iba-1 marker was used for macrophages. It has been established that connexin-43-containing structures are identified predominantly in satellite glial cells of young and aging animals. Sensory neurons, as well as DRG macrophages, of the examined age groups do not contain connexin-43. When analyzing age-related changes in intercellular contacts in the DRG of rats, it was found that areas enriched with connexin-43, corresponding to plaques of protein channels that ensure metabolic interaction of satellite glial cells in the dorsal root ganglia, became more numerous with age. This fact may indicate activation of interaction between glial cells in the sensory ganglia during rat aging.

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来源期刊
Cell and Tissue Biology
Cell and Tissue Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
0.80
自引率
0.00%
发文量
51
期刊介绍: The journal publishes papers on vast aspects of cell research, including morphology, biochemistry, biophysics, genetics, molecular biology, immunology. The journal accepts original experimental studies, theoretical articles suggesting novel principles and approaches, presentations of new hypotheses, reviews highlighting major developments in cell biology, discussions. The main objective of the journal is to provide a competent representation and integration of research made on cells (animal and plant cells, both in vivo and in cell culture) offering insight into the structure and functions of live cells as a whole. Characteristically, the journal publishes articles on biology of free-living and parasitic protists, which, unlike Metazoa, are eukaryotic organisms at the cellular level of organization.
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