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γ-氨基丁酸(GABA)刺激对大鼠培养小脑颗粒细胞中GABAA受体亚基蛋白及mRNA表达的影响。

The effect of GABA stimulation on GABAA receptor subunit protein and mRNA expression in rat cultured cerebellar granule cells.

作者信息

Platt K P, Zwartjes R E, Bristow D R

机构信息

Neuroscience Division, School of Biological Sciences, University of Manchester.

出版信息

Br J Pharmacol. 1996 Dec;119(7):1393-400. doi: 10.1111/j.1476-5381.1996.tb16051.x.

DOI:10.1111/j.1476-5381.1996.tb16051.x
PMID:8968548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1915816/
Abstract
  1. After 8 days in vitro, rat cerebellar granule cells were exposed to 1 mM gamma-aminobutyric acid (GABA) for periods of 1, 2, 4, 6, 8 and 10 days. The effect of the GABA exposure on GABAA receptor alpha 1, alpha 6 and beta 2,3 subunit protein expression and alpha 1 and alpha 6 subunit steady-state mRNA levels, was examined using Western blotting and reverse transcriptase-polymerase chain reaction (RT-PCR), respectively. 2. GABA exposure for 2 days decreased alpha 1 (35 +/- 10%, mean +/- s.e.mean), beta 2,3 (21 +/- 9%) and alpha 6 (28 +/- 10%) subunit protein expression compared to control levels. The GABA-mediated reduction in alpha 1 subunit expression after 2 days treatment was abolished in the presence of the GABAA receptor antagonist, Ru 5135 (10 microM). 3. GABA exposure for 8 days increased alpha 1 (26 +/- 10%, mean +/- s.e.mean) and beta 2,3 (56 +/- 23%) subunit protein expression over control levels, whereas alpha 6 subunit protein expression remained below control levels (by 38 +/- 10%). However, after 10 days GABA exposure, alpha 6 subunit protein expression was also increased over control levels by 65 +/- 29% (mean +/- s.e.mean). 4. GABA exposure did not change the alpha 1 or alpha 6 subunit steady-state mRNA levels over and 8 day period, nor did it alter the expression of cyclophilin mRNA over 1-8 days. 5. These results suggest that chronic GABA exposure of rat cerebellar granule cells has a bi-phasic effect on GABAA receptor subunit expression that is independent of changes to mRNA levels. Therefore, the regulation of the GABAA receptor expression by chronic agonist treatment appears to involve post-transcriptional and/or post-translational processes.
摘要
  1. 在体外培养8天后,将大鼠小脑颗粒细胞暴露于1 mM的γ-氨基丁酸(GABA)中,持续1、2、4、6、8和10天。分别使用蛋白质免疫印迹法和逆转录-聚合酶链反应(RT-PCR)检测GABA暴露对GABAA受体α1、α6和β2,3亚基蛋白表达以及α1和α6亚基稳态mRNA水平的影响。

  2. 与对照水平相比,暴露于GABA 2天可使α1(35±10%,平均值±标准误平均值)、β2,3(21±9%)和α6(28±10%)亚基蛋白表达降低。在存在GABAA受体拮抗剂Ru 5135(10 μM)的情况下,2天处理后GABA介导的α1亚基表达降低被消除。

  3. 暴露于GABA 8天可使α1(26±10%,平均值±标准误平均值)和β2,3(56±23%)亚基蛋白表达高于对照水平,而α6亚基蛋白表达仍低于对照水平(降低38±10%)。然而,在暴露于GABA 10天后,α6亚基蛋白表达也高于对照水平,增加了65±29%(平均值±标准误平均值)。

  4. 在8天的时间段内,GABA暴露未改变α1或α6亚基的稳态mRNA水平,在1 - 8天内也未改变亲环素mRNA的表达。

  5. 这些结果表明,大鼠小脑颗粒细胞长期暴露于GABA对GABAA受体亚基表达具有双相效应,且该效应与mRNA水平的变化无关。因此,长期激动剂处理对GABAA受体表达的调节似乎涉及转录后和/或翻译后过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbce/1915816/cc34cc00ab83/brjpharm00076-0108-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbce/1915816/216a91c5efa9/brjpharm00076-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbce/1915816/d52ce012cbf9/brjpharm00076-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbce/1915816/cc34cc00ab83/brjpharm00076-0108-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbce/1915816/216a91c5efa9/brjpharm00076-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbce/1915816/d52ce012cbf9/brjpharm00076-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbce/1915816/cc34cc00ab83/brjpharm00076-0108-b.jpg

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本文引用的文献

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2
Which GABAA-receptor subtypes really occur in the brain?大脑中真正存在哪些GABAA受体亚型?
Trends Neurosci. 1996 Apr;19(4):139-43. doi: 10.1016/s0166-2236(96)80023-3.
3
The alpha 1 and alpha 6 subunits can coexist in the same cerebellar GABAA receptor maintaining their individual benzodiazepine-binding specificities.
α1和α6亚基可共存于同一小脑γ-氨基丁酸A型(GABAA)受体中,保持各自的苯二氮䓬结合特异性。
J Neurochem. 1996 Feb;66(2):685-91. doi: 10.1046/j.1471-4159.1996.66020685.x.
4
Developmental cues modulate GABAA receptor subunit mRNA expression in cultured cerebellar granule neurons.发育线索调节培养的小脑颗粒神经元中GABAA受体亚基mRNA的表达。
J Neurosci. 1993 Apr;13(4):1784-92. doi: 10.1523/JNEUROSCI.13-04-01784.1993.
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Current potentiation by diazepam but not GABA sensitivity is determined by a single histidine residue.地西泮引起的当前增强作用而非GABA敏感性由单个组氨酸残基决定。
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J Biol Chem. 1993 Feb 15;268(5):3753-7.
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