Dual expression of mouse and rat VRL-1 in the dorsal root ganglion derived cell line F-11 and biochemical analysis of VRL-1 after heterologous expression.

Ricarda Jahnel, Olaf Bender, Lisa M Münter, Mathias Dreger, Clemens Gillen, Ferdinand Hucho
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引用次数: 34

Abstract

The vanilloid-like TRP-channel VRL-1 (TRPV2) is a nonselective cation channel expressed by primary sensory neurons and non-neuronal tissues [Caterina, M.J., Rosen, T.A., Tominaga, M., Brake, A.J and Julius, D. (1999) Nature 398, 436-441]. It is one of the six members of the vanilloid-like TRP-channel family which is now termed the TRPV family [Montell, G., Birnbaumer, L., Flockerzi, V., Bindels, R.J., Brutford, E.A., Caterina, M.J., Clapham, D.E., Harteneck, C., Heller, S., Julius, D., Kojima, I., Mori, Y., Penner, R., Prawitt, D., Scharenberg, A.M., Schultz, G., Shimizu, N. and Zhu, M.X. (2002) Mol. Cell 2, 229-231]. As it is a temperature-gated channel, VRL-1 appears to be functionally related to VR1. In contrast to VR1, VRL-1 is activated at a higher temperature threshold and it does not respond to capsaicin or protons. Here we describe the expression of VRL-1 in the rat dorsal root ganglion-derived cell line F-11, a hybridoma of mouse neuroblastoma (N18TG2) and rat dorsal root ganglion cells. We found by RT-PCR that F-11 cells express not only the rat VRL-1, but also its mouse orthologue in a single cell. The F-11 parental cell line N18TG2 also expressed murine VRL-1. Due to its neuronal character, the DRG-derived F-11 cell line provides an experimental system for the study of VRL-1 biochemistry. However, one has to be aware that both the mouse and the rat protein are expressed simultaneously. Furthermore we cloned VRL-1 from rat brain and analyzed its glycosylation and localization in comparison to the endogenously expressed protein in F-11 cells. In contrast to the endogenous VRL-1 the overexpressed protein is glycosylated. Similar to VR1 the glycosylation is N-linked as shown by an deglycosylation assay. Immunofluorescence analysis of the endogenous VRL-1 in F-11 cells gives only weak signals in the cytoplasm whereas the overexpressed rat VRL-1 appears mainly at the plasma membrane.

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小鼠和大鼠VRL-1在背根神经节源性细胞系F-11中的双表达及异源表达后VRL-1的生化分析。
香草素样trp通道VRL-1 (TRPV2)是主要感觉神经元和非神经元组织表达的非选择性阳离子通道[Caterina, M.J, Rosen, T.A, Tominaga, M., Brake, A.J and Julius, D. (1999) Nature 398, 436-441]。它是现在被称为TRPV家族的香兰草样trp通道家族的六个成员之一[Montell, G., Birnbaumer, L., florkerzi, V., Bindels, r.j., Brutford, E.A, Caterina, m.j., Clapham, D.E, Harteneck, C, Heller, S., Julius, D., Kojima, I., Mori, Y., Penner, R., Prawitt, D., Scharenberg, A.M, Schultz, G., Shimizu, N.和Zhu, M.X. (2002) Mol. Cell, 229-231]。由于它是一个温度门控通道,VRL-1似乎在功能上与VR1相关。与VR1相反,VRL-1在更高的温度阈值下被激活,并且对辣椒素或质子没有反应。本研究描述了VRL-1在大鼠背根神经节源性细胞系F-11、小鼠神经母细胞瘤(N18TG2)杂交瘤和大鼠背根神经节细胞中的表达。我们通过RT-PCR发现,F-11细胞在单个细胞中不仅表达大鼠VRL-1,还表达其小鼠同源基因。F-11亲本细胞系N18TG2也表达小鼠VRL-1。由于其神经元特性,drg衍生的F-11细胞系为VRL-1的生物化学研究提供了实验系统。然而,人们必须意识到,小鼠和大鼠的蛋白质是同时表达的。此外,我们从大鼠脑中克隆了VRL-1,并与F-11细胞内源性表达的VRL-1蛋白进行了糖基化和定位分析。与内源性VRL-1相反,过表达蛋白是糖基化的。与VR1类似,糖基化是n -链的,如去糖基化试验所示。F-11细胞内源性VRL-1的免疫荧光分析仅在细胞质中显示微弱信号,而过表达的大鼠VRL-1主要出现在质膜上。
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