Hao Yuchen, Tang Jingshu, Wang KeWei
1 Department of Molecular and Cellular Pharmacology, State Key Laboratory of Natural and Biomimetic Drugs, Peking University School of Pharmaceutical Sciences , Beijing, China .
Assay Drug Dev Technol. 2015 Apr;13(3):174-84. doi: 10.1089/adt.2014.622. Epub 2015 Apr 16.
The α7 nicotinic acetylcholine receptor (α7 nAChR) is an important and challenging target for drug discovery in the area of neuropsychiatric disorders. The current screening for chemicals targeting α7 nAChRs is primarily achieved by the use of low-throughput assay two-electrode voltage clamp (TEVC) in nonmammalian Xenopus oocytes. Automated patch clamp system has emerged as an attractive approach compared to conventional electrophysiology. To develop a mammalian cell-based functional assay in an automated electrophysiology system, we in this study generated a stable expression of α7 nAChRs in GH3 cells that originated from a rat pituitary tumor cell line and utilized automated QPatch-16 to test a set of tool compounds and chemicals identified as α7 agonists by TEVC. For the improvement of evaluating weak or partial α7 nAChRs agonists, we achieved enhancement of the signal-to-noise ratio by the addition of a positive allosteric modulator PNU-120596, which only activates α7 current in the presence of agonist. This improved assay was further validated by using known α7 partial agonists, such as RG3487, EVP-6124, and A-P90. Using this validated assay, we were able to identify a novel agonist 140507C that partially activates α7 nAChRs. Taken together, our results validate the use of QPatch-16 for evaluation α7 partial agonists, demonstrating its utility as an effective tool for α7 ion channel drug discovery.
α7烟碱型乙酰胆碱受体(α7 nAChR)是神经精神疾病药物研发领域一个重要且具有挑战性的靶点。目前针对α7 nAChRs的化学物质筛选主要通过在非哺乳动物非洲爪蟾卵母细胞中使用低通量双电极电压钳(TEVC)检测来实现。与传统电生理学相比,自动膜片钳系统已成为一种有吸引力的方法。为了在自动电生理系统中开发基于哺乳动物细胞的功能检测方法,我们在本研究中使源自大鼠垂体肿瘤细胞系的GH3细胞稳定表达α7 nAChRs,并利用自动QPatch-16检测一组经TEVC鉴定为α7激动剂的工具化合物和化学物质。为了改进对弱或部分α7 nAChRs激动剂的评估,我们通过添加正变构调节剂PNU-120596提高了信噪比,该调节剂仅在激动剂存在时激活α7电流。使用已知的α7部分激动剂,如RG3487、EVP-6124和A-P90,进一步验证了这种改进的检测方法。使用这种经过验证的检测方法,我们能够鉴定出一种新型激动剂140507C,它能部分激活α7 nAChRs。综上所述,我们的结果验证了使用QPatch-16评估α7部分激动剂的有效性,证明了其作为α7离子通道药物研发有效工具的实用性。