Brooks-Kayal A R, Shumate M D, Jin H, Lin D D, Rikhter T Y, Holloway K L, Coulter D A
Pediatric Regional Epilepsy Program and Joseph Stokes Research Institute of The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
J Neurosci. 1999 Oct 1;19(19):8312-8. doi: 10.1523/JNEUROSCI.19-19-08312.1999.
gamma-Aminobutyric acid(A) receptors (GABARs) are heteromeric proteins composed of multiple subunits. Numerous subunit subtypes are expressed in individual neurons, which assemble in specific preferred GABAR configurations. Little is known, however, about the coordination of subunit expression within individual neurons or the impact this may have on GABAR function. To investigate this, it is necessary to profile quantitatively the expression of multiple subunit mRNAs within individual cells. In this study, single-cell antisense RNA amplification was used to examine the expression of 14 different GABAR subunit mRNAs simultaneously in individual human dentate granule cells (DGCs) harvested during hippocampectomy for intractable epilepsy. alpha4, beta2, and delta-mRNA levels were tightly correlated within individual DGCs, indicating that these subunits are expressed coordinately. Levels of alpha3- and beta2-mRNAs, as well as epsilon- and beta1-mRNAs, also were strongly correlated. No other subunit correlations were identified. Coordinated expression could not be explained by the chromosomal clustering of GABAR genes and was observed in control and epileptic rats as well as in humans, suggesting that it was not species-specific or secondary to epileptogenesis. Benzodiazepine augmentation of GABA-evoked currents also was examined to determine whether levels of subunit mRNA expression correlated with receptor pharmacology. This analysis delineated two distinct cell populations that differed in clonazepam modulation and patterns of alpha-subunit expression. Clonazepam augmentation correlated positively with the relative expression of alpha1- and gamma2-mRNAs and negatively with alpha4- and delta-mRNAs. These data demonstrate that specific GABAR subunit mRNAs exhibit coordinated control of expression in individual DGCs, which has significant impact on inhibitory function.
γ-氨基丁酸(A)受体(GABARs)是由多个亚基组成的异源蛋白。众多亚基亚型在单个神经元中表达,它们以特定的偏好GABAR构型组装。然而,关于单个神经元内亚基表达的协调情况或其对GABAR功能可能产生的影响,人们知之甚少。为了研究这一点,有必要定量分析单个细胞内多个亚基mRNA的表达情况。在本研究中,单细胞反义RNA扩增技术被用于同时检测在因顽固性癫痫而进行海马切除术时采集的单个人类齿状颗粒细胞(DGCs)中14种不同GABAR亚基mRNA的表达。在单个DGCs中,α4、β2和δ-mRNA水平紧密相关,表明这些亚基是协同表达的。α3-和β2-mRNA水平,以及ε-和β1-mRNA水平也高度相关。未发现其他亚基之间的相关性。协同表达无法用GABAR基因的染色体聚类来解释,并且在对照大鼠和癫痫大鼠以及人类中均观察到,这表明它不是物种特异性的,也不是癫痫发生的继发结果。还检测了苯二氮䓬增强GABA诱发电流的情况,以确定亚基mRNA表达水平是否与受体药理学相关。该分析划分出了两个不同的细胞群体,它们在氯硝西泮调节和α-亚基表达模式上存在差异。氯硝西泮增强作用与α1-和γ2-mRNA的相对表达呈正相关,与α4-和δ-mRNA呈负相关。这些数据表明,特定的GABAR亚基mRNA在单个DGCs中表现出对表达的协同控制,这对抑制功能有重大影响。