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原代培养的小脑颗粒细胞中,环磷酸腺苷介导的信号机制对GABAA受体α1和α6亚基表达的双向调节

Bidirectional regulation of GABAA receptor alpha1 and alpha6 subunit expression by a cyclic AMP-mediated signalling mechanism in cerebellar granule cells in primary culture.

作者信息

Thompson C L, Pollard S, Stephenson F A

机构信息

Department of Pharmaceutical and Biological Chemistry, School of Pharmacy, University of London, England.

出版信息

J Neurochem. 1996 Jul;67(1):434-7. doi: 10.1046/j.1471-4159.1996.67010434.x.

Abstract

Forskolin treatment of cerebellar granule cells in culture resulted in bidirectional regulation of the expression of GABAA receptor alpha1 and alpha6 subunits. Thus, forskolin applied at 2 days in vitro (DIV) increased expression of the alpha1 subunit but decreased the expression of the alpha6 subunit. Values with respect to control cultures, both assayed at 9 DIV by immunoblotting, were 310 +/- 48% for alpha1 and 25 +/- 16% for the alpha6 subunit. Similar effects were evoked following chronic treatment with both dibutyryl cyclic AMP and 3-isobutyl-1-methylxanthine. Dideoxyforskolin had no effect on the level of expression of either the alpha1 or the alpha6 GABAA receptor subunits. The changes in subunit expression were accompanied by a 1.7-fold increase in number of total specific [3H]Ro 15-4513 binding sites expressed by intact cerebellar granule cells. This increase in total binding sites was accommodated by a 2.7-fold increase in number of diazepam-sensitive Ro 15-4513 binding sites in accordance with the observed increase in alpha1 subunit expression. The number of diazepam-insensitive subtype of binding sites were not significantly changed. These results suggest that GABAA receptor subtype expression can be differentially regulated by intracellular cyclic AMP concentration.

摘要

在培养的小脑颗粒细胞中,福斯高林处理导致GABAA受体α1和α6亚基表达的双向调节。因此,在体外培养2天(DIV)时应用福斯高林会增加α1亚基的表达,但会降低α6亚基的表达。通过免疫印迹在9 DIV时对对照培养物进行检测,α1亚基相对于对照培养物的值为310±48%,α6亚基为25±16%。用二丁酰环磷酸腺苷和3-异丁基-1-甲基黄嘌呤进行慢性处理后也会产生类似的效果。双脱氧福斯高林对α1或α6 GABAA受体亚基的表达水平没有影响。亚基表达的变化伴随着完整小脑颗粒细胞表达的总特异性[3H]Ro 15-4513结合位点数量增加1.7倍。根据观察到的α1亚基表达增加,总结合位点的这种增加与地西泮敏感的Ro 15-4513结合位点数量增加2.7倍相一致。地西泮不敏感的结合位点亚型数量没有显著变化。这些结果表明,GABAA受体亚型表达可受细胞内环磷酸腺苷浓度的差异调节。

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