Cappuccio Irene, Spinsanti Paola, Porcellini Antonio, Desiderati Francesca, De Vita Teresa, Storto Marianna, Capobianco Loredana, Battaglia Giuseppe, Nicoletti Ferdinando, Melchiorri Daniela
Department of Human Physiology and Pharmacology, University of Rome La Sapienza, Piazzale Aldo Moro 5, 00185 Rome, Italy.
Neuropharmacology. 2005;49 Suppl 1:196-205. doi: 10.1016/j.neuropharm.2005.05.014.
Cultured mouse embryonic stem (ES) cells maintained under undifferentiated conditions (i.e. grown in medium containing 15% FCS and leukemia inhibitory factor--LIF) expressed mGlu5 metabotropic glutamate receptors. Activation of these receptors with quisqualate increased [Ca2+]i but only when cultures were deprived of extracellular glutamate, indicating that the receptor was saturated by the endogenous glutamate. Pharmacological blockade of mGlu5 receptors with 2-methyl-6-(phenylethynyl)pyridine (MPEP) or antisense-induced knock-down of mGlu5 receptors decreased the expression of the two main transcription factors that sustain ES cell self-renewal, i.e. Oct-4 and Nanog, as assessed by real-time PCR and immunoblotting. Exposure of ES cell cultures to MPEP also reduced alkaline phosphatase activity, a marker of undifferentiated ES cells. These data support a critical role for mGlu receptors in early development showing that mGlu5 receptors are expressed by ES cells and their activation sustains ES cell self-renewal in culture.
在未分化条件下培养的小鼠胚胎干细胞(ES细胞)(即在含有15%胎牛血清和白血病抑制因子——LIF的培养基中生长)表达代谢型谷氨酸受体mGlu5。用喹啉酸激活这些受体可增加细胞内钙离子浓度([Ca2+]i),但仅在培养物中细胞外谷氨酸被去除时才会增加,这表明该受体被内源性谷氨酸饱和。用2-甲基-6-(苯乙炔基)吡啶(MPEP)对mGlu5受体进行药理阻断或通过反义诱导敲低mGlu5受体,会降低维持ES细胞自我更新的两个主要转录因子Oct-4和Nanog的表达,这是通过实时PCR和免疫印迹评估得出的。将ES细胞培养物暴露于MPEP也会降低碱性磷酸酶活性,碱性磷酸酶是未分化ES细胞的一个标志物。这些数据支持了代谢型谷氨酸受体在早期发育中的关键作用,表明ES细胞表达mGlu5受体,且其激活维持了培养中的ES细胞自我更新。