Oka Michiko, Wada Miyuki, Wu Qiang, Yamamoto Akira, Fujita Takuya
Department of Biochemical Pharmacology, Kyoto Pharmaceutical University, Misasagi, Kyoto, Japan.
Biochem Biophys Res Commun. 2006 Mar 17;341(3):874-81. doi: 10.1016/j.bbrc.2006.01.039. Epub 2006 Jan 23.
GABA(B) receptor subunits are widely expressed on neurons throughout the central nervous system (CNS), at both pre- and postsynaptic sites, where they mediate the late and slow component of the inhibitory response to the major inhibitory neurotransmitter GABA. Recently, GABA(B) receptors have been reported to be expressed in astrocytes and microglia in the rat CNS by immunocytochemistry. However, there are few reports available for the functional characterization of GABA(B) receptors on astrocytes. In the present study, we therefore investigated the functional expression and characteristics of GABA(B) receptors in primary cultures of astrocytes from rat cerebral cortex. In the presence of 10 microM GTP, forskolin concentration-dependently increased adenylylcyclase (AC) activity in membranes prepared from rat astrocytes. The selective GABA(B) agonist (R)-baclofen concentration-dependently reduced forskolin-stimulated AC activity in the presence of 10 microM GTP. This effect was reversed by the selective GABA(B) antagonists, CGP-55845 and CGP-54626, and was completely abolished by treatment of astrocytic membranes with pertussis toxin. In addition, RT-PCR, Western blotting, and immunocytochemistry clearly showed that metabotropic GABA(B) receptor isoforms (GABA(B)R1 and GABA(B)R2) are expressed in rat cerebrocortical astrocytes. Taken collectively, these results demonstrate that functionally active metabotropic GABA(B) receptors are expressed in rat cerebrocortical astrocytes.
GABA(B)受体亚基在整个中枢神经系统(CNS)的神经元上广泛表达,存在于突触前和突触后位点,在这些位点它们介导对主要抑制性神经递质GABA抑制反应的晚期和缓慢成分。最近,通过免疫细胞化学已报道GABA(B)受体在大鼠CNS的星形胶质细胞和小胶质细胞中表达。然而,关于星形胶质细胞上GABA(B)受体功能特性的报道很少。因此,在本研究中,我们研究了大鼠大脑皮质星形胶质细胞原代培养物中GABA(B)受体的功能表达和特性。在存在10微摩尔GTP的情况下,福斯高林浓度依赖性地增加了从大鼠星形胶质细胞制备的膜中的腺苷酸环化酶(AC)活性。在存在10微摩尔GTP的情况下,选择性GABA(B)激动剂(R)-巴氯芬浓度依赖性地降低了福斯高林刺激的AC活性。这种作用被选择性GABA(B)拮抗剂CGP-55845和CGP-54626逆转,并且通过用百日咳毒素处理星形胶质细胞膜而完全消除。此外,逆转录-聚合酶链反应(RT-PCR)、蛋白质免疫印迹和免疫细胞化学清楚地表明,代谢型GABA(B)受体亚型(GABA(B)R1和GABA(B)R2)在大鼠脑皮质星形胶质细胞中表达。总的来说,这些结果表明功能性活性代谢型GABA(B)受体在大鼠脑皮质星形胶质细胞中表达。