Neuroscience Program and Department of Zoology & Physiology, University of Wyoming, 1000 E University Avenue, Laramie, WY 82071, USA.
Neuroscience. 2010 Nov 10;170(4):1020-7. doi: 10.1016/j.neuroscience.2010.08.015. Epub 2010 Aug 13.
The tachykinin NK3 receptor (NK3R) is a G-protein coupled receptor that is activated, internalized, and trafficked to the nuclei of magnocellular neurons in the paraventricular nucleus of the hypothalamus (PVN) in response to acute hyperosmolarity. The lack of information on the nuclear import pathway raises concerns about the physiological role of nuclear NK3R. NK3R contains a nuclear localizing sequence (NLS) and this raises the possibility that importins are involved in transport of NK3R through the nuclear pore complex. The following experiments utilized: (1) co-immunoprecipitation to determine if NK3R is associated with importin ß-1 following activation in response to acute hyperosmolarity in vivo, and (2) immuno-neutralization of importin ß-1 in vitro to determine if nuclear transport of NK3R was blocked. Rats were given an i.v. injection of hypertonic saline (2 M) and 10 min after the infusion, the PVN was removed and homogenized. Importin ß-1 co-immunoprecipitated with the NK3R following treatment with 2 M NaCl, but not following isotonic saline treatment. Immuno-neutralization of importin ß-1 decreased the transport of NK3R into the nuclei in a time dependent fashion. The results indicate that in response to acute hyperosmotic challenge, NK3R associates with importin ß-1 which enables the nuclear transport of NK3R. This is the first in vivo study linking importin ß-1 and the nuclear transport of a G protein coupled receptor, the NK3R, in brain.
速激肽 NK3 受体(NK3R)是一种 G 蛋白偶联受体,在急性高渗刺激下,它会被激活、内化,并转运到下丘脑室旁核(PVN)的大细胞神经元核内。由于缺乏关于核内导入途径的信息,人们对核 NK3R 的生理作用产生了担忧。NK3R 含有一个核定位序列(NLS),这就提出了一种可能性,即导入蛋白可能参与 NK3R 通过核孔复合物的运输。以下实验利用了:(1)共免疫沉淀法,以确定在体内急性高渗刺激下激活后,NK3R 是否与导入蛋白β-1 相关联;(2)体外免疫中和导入蛋白β-1,以确定 NK3R 的核转运是否被阻断。给大鼠静脉注射高渗盐水(2 M),在输注后 10 分钟,取出 PVN 并匀浆。在 2 M NaCl 处理后,NK3R 与导入蛋白β-1 共沉淀,但在等渗盐水处理后没有。导入蛋白β-1 的免疫中和以时间依赖的方式降低了 NK3R 向核内的转运。结果表明,在急性高渗刺激下,NK3R 与导入蛋白β-1 结合,从而使 NK3R 能够进行核转运。这是首例在体内将导入蛋白β-1 与 G 蛋白偶联受体 NK3R 的核转运联系起来的研究。