Zheng T M, Zhu W J, Puia G, Vicini S, Grayson D R, Costa E, Caruncho H J
Fidia-Georgetown Institute for the Neurosciences, Georgetown University School of Medicine, Washington, DC 20007.
Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):10952-6. doi: 10.1073/pnas.91.23.10952.
The amounts of mRNAs encoding alpha 1, alpha 6, beta 2, beta 3, gamma 2, and delta subunits of gamma-aminobutyrate type A (GABAA) receptors and the gold immunolabeling density of their translation products were monitored during the growth of neonatal rat granule cells in primary culture. We investigated possible correlations (i) between temporal changes in mRNA content and expression density of their respective translation products and (ii) between the quantitative changes of receptor subunit expression, the GABA EC50 for Cl- channel activation, and diazepam efficacy in modulating GABA action on the Cl- channels. At 3 days in vitro, the amount of GABAA receptor subunit mRNAs and the expression of their respective translation products were very low. During the next 2 weeks both parameters for every subunit studied increased asynchronously; moreover, at 14 days in vitro the sum of gamma 2 and delta subunit expression was smaller than the expression of the alpha 1 or alpha 6 or beta 2/beta 3 subunits. This suggests that during in vitro maturation each subunit may be regulated independently and invites speculation as to possible changes in specific GABAA receptor subtype abundance during development in vitro. The maximal current intensity elicited by GABA failed to increase from 5 to 14 days in vitro, though the amount of mRNA encoding various subunits and the expression density of their respective translation products increased. Thus, qualitative changes in the GABAA receptor subtypes expressed and/or abnormalities in the subunit assembly very likely account for the uniformity of the maximal current intensity elicited by GABA during in vitro development. Also, during maturation of neuronal cultures from 5 to 20 days in vitro the extent of the positive modulation of GABA action by diazepam decreased dramatically. This finding might be related to an increase in the abundance of GABAA receptors including the alpha 6 subunit and/or to the expression, during granule cell maturation in vitro, of GABAA receptors devoid of gamma 2 subunits.
在原代培养的新生大鼠颗粒细胞生长过程中,监测了编码γ-氨基丁酸A型(GABAA)受体α1、α6、β2、β3、γ2和δ亚基的mRNA量及其翻译产物的金免疫标记密度。我们研究了以下可能的相关性:(i)mRNA含量的时间变化与其各自翻译产物的表达密度之间的相关性;(ii)受体亚基表达的定量变化、GABA激活氯离子通道的半数有效浓度(EC50)以及地西泮调节GABA对氯离子通道作用的效力之间的相关性。在体外培养3天时,GABAA受体亚基mRNA的量及其各自翻译产物的表达非常低。在接下来的2周内,所研究的每个亚基的这两个参数均异步增加;此外,在体外培养14天时,γ2和δ亚基表达的总和小于α1或α6或β2/β3亚基的表达。这表明在体外成熟过程中,每个亚基可能受到独立调节,并引发了关于体外发育过程中特定GABAA受体亚型丰度可能变化的推测。尽管编码各种亚基的mRNA量及其各自翻译产物的表达密度增加,但GABA引发的最大电流强度在体外培养5至14天期间未能增加。因此,体外发育过程中GABAA受体亚型表达的定性变化和/或亚基组装异常很可能是GABA引发的最大电流强度保持一致的原因。此外,在神经元培养物从体外培养5天到20天的成熟过程中,地西泮对GABA作用的正向调节程度显著降低。这一发现可能与包括α6亚基在内的GABAA受体丰度增加和/或与体外颗粒细胞成熟过程中缺乏γ2亚基的GABAA受体的表达有关。