Wakakura M, Utsunomiya-Kawasaki I, Ishikawa S
Department of Ophthalmology, Kitasato University School of Medicine, Sagamihara, Japan.
Graefes Arch Clin Exp Ophthalmol. 1998 Dec;236(12):934-9. doi: 10.1007/s004170050183.
This study was conducted to detect the presence of muscarinic or nicotinic receptors in cultured retinal neurons and Müller cells.
Pure Müller cell cultures and cocultures of retinal neurons and Müller cells were used; the former, obtained from adult rabbit retinas, and the latter, retinal neurons from neonatal rats, were cocultured with Müller cells. Intracellular calcium ion concentration ([Ca2+]i) following the administration of acetylcholine, a cholinesterase inhibitor (trichlorfon), nicotine or muscarinic agonist with or without a receptor antagonist was monitored using the calcium ion indicator, fura-2.
Acetylcholine and trichlorfon induced rapid increase in [Ca2+]i in half of either cell type. Trichlorfon induced positive response in coculture but not in the pure Müller cell cultures. This positive response was blocked only partially in the presence of atropine. Approximately 30-40% of neurons responded to nicotine at 5 microM, which was significantly blocked by alpha-bungarotoxin at 50 nM. No response to nicotine could be detected in Müller cells. Approximately 50% of neurons responded to muscarine at 50 microM, but 500 microM was required for the formation of calcium transients in 50% of Müller cells. The muscarine inducement of rapid increase in [Ca2+]i was blocked by atropine. The agonist of M1 (a muscarinic receptor subtype), McN-A-343, at 0.5 microM induced the most significant and rapid increase in [Ca2+]i both in neurons and Müller cells. McN-A-343 administration at 0.05 microM induced positive response in half the neurons, but only in approximately 10% of Müller cells. Such positive response was not observed following preincubation with the M1 antagonist, pirenzepine, at 50 microM.
Cocultured retinal neurons enhance the release of acetylcholine following anticholinesterase administration, and approximately half the neurons were found to possess muscarinic and nicotinic receptors. However, Müller cells appeared to possess only the less sensitive muscarinic receptor. Muscarinic receptor subtypes on either type of cell contained at least M1.
本研究旨在检测培养的视网膜神经元和 Müller 细胞中是否存在毒蕈碱型或烟碱型受体。
使用纯 Müller 细胞培养物以及视网膜神经元与 Müller 细胞的共培养物;前者取自成年兔视网膜,后者的视网膜神经元来自新生大鼠,并与 Müller 细胞共培养。使用钙离子指示剂 fura-2 监测在给予乙酰胆碱、一种胆碱酯酶抑制剂(敌百虫)、尼古丁或毒蕈碱激动剂(有无受体拮抗剂)后细胞内钙离子浓度([Ca2+]i)的变化。
乙酰胆碱和敌百虫在两种细胞类型中的半数细胞中诱导[Ca2+]i 快速升高。敌百虫在共培养物中诱导出阳性反应,但在纯 Müller 细胞培养物中未出现。在阿托品存在的情况下,这种阳性反应仅被部分阻断。约 30 - 40%的神经元对 5 μM 的尼古丁有反应,50 nM 的α-银环蛇毒素可显著阻断该反应。在 Müller 细胞中未检测到对尼古丁的反应。约 50%的神经元对 50 μM 的毒蕈碱有反应,但 500 μM 才能使 50%的 Müller 细胞形成钙瞬变。毒蕈碱诱导的[Ca2+]i 快速升高被阿托品阻断。M1(一种毒蕈碱受体亚型)的激动剂 McN-A-343 在 0.5 μM 时,在神经元和 Müller 细胞中均诱导出最显著且快速的[Ca2+]i 升高。0.05 μM 的 McN-A-343 给药在半数神经元中诱导出阳性反应,但仅在约 10%的 Müller 细胞中出现。在与 50 μM 的 M1 拮抗剂哌仑西平预孵育后未观察到这种阳性反应。
共培养的视网膜神经元在给予抗胆碱酯酶药物后增强乙酰胆碱的释放,并且发现约半数神经元同时拥有毒蕈碱型和烟碱型受体。然而,Müller 细胞似乎仅拥有敏感性较低的毒蕈碱型受体。两种细胞类型上的毒蕈碱受体亚型至少包含 M1。