Bianchi Bruce R, Lee Chih-Hung, Jarvis Michael F, El Kouhen Rachid, Moreland Robert B, Faltynek Connie R, Puttfarcken Pamela S
Neuroscience Research, Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, IL 60064, USA.
Eur J Pharmacol. 2006 May 10;537(1-3):20-30. doi: 10.1016/j.ejphar.2006.03.003. Epub 2006 Mar 10.
The transient receptor potential vanilloid 1 (TRPV1) receptor is a ligand-gated cation channel that can be activated by capsaicin, heat, protons and cytosolic lipids. We compared activation of recombinant human TRPV1 receptors stably expressed in human 293 cells, derived from kidney embryonic cells, and in human 1321N1 cells, derived from brain astrocytes. Cellular influx of calcium was measured in response to acid, endovanilloids (N-arachidonoyl-dopamine, N-oleoyl-dopamine and anandamide), capsaicin and other traditional vanilloid agonists under normal (pH 7.4) and acidic (pH 6.7 and 6.0) assay conditions. The host cell expression system altered the agonist profile of endogenous TRPV1 receptor agonists without affecting the pharmacological profile of either exogenous TRPV1 receptor agonists or antagonists. Our data signify that the host cell expression system plays a modulatory role in TRPV1 receptor activity, and suggests that activation of native human TRPV1 receptors in vivo will be dependent on cell-specific regulatory factors/pathways.
瞬时受体电位香草酸亚型1(TRPV1)受体是一种配体门控阳离子通道,可被辣椒素、热、质子和胞质脂质激活。我们比较了稳定表达于源自肾胚胎细胞的人293细胞和源自脑星形胶质细胞的人1321N1细胞中的重组人TRPV1受体的激活情况。在正常(pH 7.4)和酸性(pH 6.7和6.0)检测条件下,测量了细胞对酸、内源性香草酸类物质(N-花生四烯酰多巴胺、N-油酰多巴胺和花生四烯乙醇胺)、辣椒素及其他传统香草酸类激动剂的钙内流情况。宿主细胞表达系统改变了内源性TRPV1受体激动剂的激动剂谱,而不影响外源性TRPV1受体激动剂或拮抗剂的药理学谱。我们的数据表明宿主细胞表达系统在TRPV1受体活性中起调节作用,并提示体内天然人TRPV1受体的激活将依赖于细胞特异性调节因子/途径。