分选连接蛋白 27 调节 G 蛋白门控内向整流钾通道,从而减弱体内可卡因反应。
Sorting nexin 27 regulation of G protein-gated inwardly rectifying K⁺ channels attenuates in vivo cocaine response.
机构信息
Peptide Biology Laboratories, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Graduate Program in Biology, University of California, San Diego, La Jolla, CA 92093, USA.
Peptide Biology Laboratories, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA; Graduate Program in Biology, University of California, San Diego, La Jolla, CA 92093, USA; Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
出版信息
Neuron. 2014 May 7;82(3):659-69. doi: 10.1016/j.neuron.2014.03.011.
The subcellular pathways that regulate G protein-gated inwardly rectifying potassium (GIRK or Kir3) channels are important for controlling the excitability of neurons. Sorting nexin 27 (SNX27) is a PDZ-containing protein known to bind GIRK2c/GIRK3 channels, but its function in vivo is poorly understood. Here, we investigated the role of SNX27 in regulating GIRK currents in dopamine (DA) neurons of the ventral tegmental area (VTA). Mice lacking SNX27 in DA neurons exhibited reduced GABABR-activated GIRK currents but had normal Ih currents and DA D2R-activated GIRK currents. Expression of GIRK2a, an SNX27-insensitive splice variant, restored GABABR-activated GIRK currents in SNX27-deficient DA neurons. Remarkably, mice with significantly reduced GABABR-activated GIRK currents in only DA neurons were hypersensitive to cocaine and could be restored to a normal locomotor response with GIRK2a expression. These results identify a pathway for regulating excitability of VTA DA neurons, highlighting SNX27 as a promising target for treating addiction.
调节 G 蛋白门控内向整流钾 (GIRK 或 Kir3) 通道的细胞内途径对于控制神经元的兴奋性很重要。分选连接蛋白 27 (SNX27) 是一种含有 PDZ 结构域的蛋白,已知其与 GIRK2c/GIRK3 通道结合,但在体内的功能知之甚少。在这里,我们研究了 SNX27 在调节腹侧被盖区 (VTA) 多巴胺 (DA) 神经元中 GIRK 电流中的作用。在 DA 神经元中缺乏 SNX27 的小鼠表现出 GABABR 激活的 GIRK 电流减少,但 Ih 电流和 DA D2R 激活的 GIRK 电流正常。表达 SNX27 不敏感的剪接变异体 GIRK2a 可恢复 SNX27 缺陷型 DA 神经元中的 GABABR 激活的 GIRK 电流。值得注意的是,只有 DA 神经元中 GABABR 激活的 GIRK 电流显著减少的小鼠对可卡因敏感,并且可以通过表达 GIRK2a 恢复正常的运动反应。这些结果确定了调节 VTA DA 神经元兴奋性的途径,突出了 SNX27 作为治疗成瘾的有前途的靶点。