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少突胶质细胞信号转导系统受神经元接触调节。

Oligodendroglial signal transduction systems are regulated by neuronal contact.

作者信息

He M, Howe D G, McCarthy K D

机构信息

Department of Pharmacology, University of North Carolina at Chapel Hill 27599, USA.

出版信息

J Neurochem. 1996 Oct;67(4):1491-9. doi: 10.1046/j.1471-4159.1996.67041491.x.

Abstract

Previous reports indicate that oligodendrocytes express signaling systems activated by classical neurotransmitters. Several signaling systems linked to mobilization of intracellular calcium have been demonstrated, and some of these are developmentally lost in vitro and in vivo. The experiments described here use oligodendrocyte-neuron cocultures to examine the effects of neuronal contact on the expression of these signaling pathways. Neonatal rat cerebral oligodendrocytes in contact with dorsal root ganglia (DRG) neurites responded to bath application of histamine, ATP, carbachol, glutamate, or bradykinin with increases in intracellular Ca2+ concentration. Similar results were obtained in coculture with superior cervical ganglia neurons. Preventing neuronal contact by transection of DRG neurites significantly reduced the percentage of oligodendrocytes responsive to each ligand, with the exception of bradykinin responsiveness, which was unaffected. Oligodendroglia isolated from adult rat spinal cord were also examined for responsiveness to these neuroligands. Few isolated adult oligodendroglia were responsive to these ligands, and coculture with DRG neurons failed to restore responsiveness. Neuroligand responsiveness was not induced in oligodendrocytes maintained 8 days in purified culture before establishment of cocultures. A significant reduction in the number of neuroligand-responsive oligodendroglia was noted for histamine, carbachol, glutamate, and ATP after including tetrodotoxin for the final 6 days of coculture. These results suggest that both neuronal contact and neuronal activity contribute to the maintenance of functional neurotransmitter-activated signaling pathways coupled to mobilization of intracellular calcium in oligodendrocytes.

摘要

先前的报道表明,少突胶质细胞表达由经典神经递质激活的信号系统。已经证实了几种与细胞内钙动员相关的信号系统,其中一些在体外和体内发育过程中会丧失。本文所述的实验使用少突胶质细胞 - 神经元共培养物来研究神经元接触对这些信号通路表达的影响。与背根神经节(DRG)神经突接触的新生大鼠脑少突胶质细胞,在浴加组胺、ATP、卡巴胆碱、谷氨酸或缓激肽后,细胞内Ca2+浓度升高。与颈上神经节神经元共培养也得到了类似结果。通过切断DRG神经突来阻止神经元接触,显著降低了对每种配体有反应的少突胶质细胞的百分比,但缓激肽反应性不受影响。还检测了从成年大鼠脊髓分离的少突胶质细胞对这些神经配体的反应性。很少有分离的成年少突胶质细胞对这些配体有反应,与DRG神经元共培养也未能恢复反应性。在建立共培养之前,在纯化培养中维持8天的少突胶质细胞未诱导出神经配体反应性。在共培养的最后6天加入河豚毒素后,观察到组胺、卡巴胆碱、谷氨酸和ATP的神经配体反应性少突胶质细胞数量显著减少。这些结果表明,神经元接触和神经元活动都有助于维持与少突胶质细胞内钙动员相关的功能性神经递质激活信号通路。

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