Poulter M O, Ohannesian L, Larmet Y, Feltz P
Institut de Physiologie, Université Louis Pasteur, Strasbourg, France.
J Neurochem. 1997 Feb;68(2):631-9. doi: 10.1046/j.1471-4159.1997.68020631.x.
The expression of six mRNA species (alpha 2, alpha 3, alpha 5, beta 2, beta 3, and gamma 2) encoding for GABAA receptor subunits was followed in cultured early postnatal cortical neurons by in situ hybridization histochemistry. In untreated control cultures it was found that these subunit mRNA expression profiles closely follow those seen during development in vivo. alpha 3, alpha 5, and beta 3 subunit expression declined, alpha 2 expression increased, whereas beta 2 and gamma 2 subunit mRNA expression remained relatively constant. To test the hypothesis that GABAA receptor stimulation regulates these expression profiles, we tested the effect of a GABAA receptor positive modulator, allopregnanolone, and a GABAA receptor noncompetitive antagonist, tert-butylbicyclophosphorothionate (TBPS). It was found that allopregnanolone augmented the rate at which the alpha 3, alpha 5, or beta 3 subunit mRNA expression declined and prevented the increase in alpha 2 subunit mRNA expression. As well, allopregnanolone down-regulated beta 2 subunit mRNA expression. TBPS, on the other hand, up-regulated alpha 3, alpha 5, beta 2, and beta 3 subunit mRNA expression. It also down-regulated the expression of alpha 2 subunit mRNA. Both allopregnanolone and TBPS had no effect on gamma 2 subunit mRNA expression. These results imply that the developmental switchover of GABA receptor subunit mRNA expression is regulated by GABAA receptor activity.
通过原位杂交组织化学方法,追踪了出生后早期培养的皮质神经元中编码GABAA受体亚基的六种mRNA种类(α2、α3、α5、β2、β3和γ2)的表达情况。在未经处理的对照培养物中发现,这些亚基mRNA的表达谱与体内发育过程中观察到的情况密切相符。α3、α5和β3亚基的表达下降,α2表达增加,而β2和γ2亚基mRNA的表达保持相对恒定。为了验证GABAA受体刺激调节这些表达谱的假设,我们测试了GABAA受体阳性调节剂别孕烯醇酮和GABAA受体非竞争性拮抗剂叔丁基双环磷硫酰胺(TBPS)的作用。结果发现,别孕烯醇酮提高了α3、α5或β3亚基mRNA表达下降的速率,并阻止了α2亚基mRNA表达的增加。此外,别孕烯醇酮下调了β2亚基mRNA的表达。另一方面,TBPS上调了α3、α5、β2和β3亚基mRNA的表达。它还下调了α2亚基mRNA的表达。别孕烯醇酮和TBPS对γ2亚基mRNA的表达均无影响。这些结果表明,GABAA受体亚基mRNA表达的发育转换受GABAA受体活性的调节。