Johnson R M, McNeeley P A, DeMoor K, Stewart G R, Glaeser B S, Pitchford S
Department of Neurosciences, Syntex Discovery Research, Palo Alto, CA 94304.
Brain Res. 1994 May 23;646(2):327-31. doi: 10.1016/0006-8993(94)90100-7.
Information on the transmembrane signaling events and subsequent biochemical processes initiated by ciliary neurotrophic factor (CNTF) receptor activation in neurons is lacking. SH-SY5Y cells, a human neuroblastoma cell line expressing CNTF receptors, were used to study metabolic changes associated with functional ligand-receptor interactions. Real-time measurements quantifying the rate of extracellular acidification by SH-SY5Y cells (a measure of metabolic activity) were made using a silicon-based cytosensor. Application of recombinant human CNTF (rhCNTF) to resting SH-SY5Y cells increased their acidification rate in a concentration and time-dependent manner with an apparent EC50 of 60 ng/ml. Pretreatment of cells with phosphatidylinositol-specific phospholipase C (PI-PLC) prevented the CNTF, but not an NGF-stimulated increase in acidification rate. Collectively, these results demonstrate that: (1) SH-SY5Y cells express functional CNTF receptors; and (2) the initial signal transduction mechanism activated by the CNTF receptor in SH-SY5Y cells is distinct from that activated by the NGF receptor; however, both may ultimately stimulate the same downstream biochemical messengers to increase cellular metabolism.
目前尚缺乏关于睫状神经营养因子(CNTF)受体激活神经元后引发的跨膜信号转导事件及后续生化过程的信息。人神经母细胞瘤细胞系SH-SY5Y细胞表达CNTF受体,被用于研究与功能性配体-受体相互作用相关的代谢变化。使用基于硅的细胞传感器对SH-SY5Y细胞胞外酸化速率(一种代谢活性的度量指标)进行实时定量测量。将重组人CNTF(rhCNTF)应用于静息的SH-SY5Y细胞,可使其酸化速率呈浓度和时间依赖性增加,表观半数有效浓度(EC50)为60 ng/ml。用磷脂酰肌醇特异性磷脂酶C(PI-PLC)预处理细胞可阻止CNTF诱导的酸化速率增加,但不能阻止神经生长因子(NGF)刺激引起的酸化速率增加。总体而言,这些结果表明:(1)SH-SY5Y细胞表达功能性CNTF受体;(2)SH-SY5Y细胞中CNTF受体激活的初始信号转导机制与NGF受体激活的机制不同;然而,两者最终可能刺激相同的下游生化信使以增加细胞代谢。