Stowell J N, Craig A M
Department of Cell and Structural Biology, University of Illinois, Urbana 61801, USA.
Neuron. 1999 Mar;22(3):525-36. doi: 10.1016/s0896-6273(00)80707-2.
The subcellular targeting of neurotransmitter receptors is vital in controlling polarized information flow in the brain. We show here that metabotropic glutamate receptors are differentially targeted when expressed from defective viral vectors in cultured hippocampal neurons; mGluR1a and mGluR2 are targeted to dendrites and excluded from axons, whereas mGluR7 is targeted to axons and dendrites. Chimeras and deletions revealed that axon exclusion of mGluR2 versus axon targeting of mGluR7 is mediated by their 60 amino acid C-terminal cytoplasmic domains. Addition of the mGluR7 C-terminal sequence to mGluR2 or to the unrelated somatodendritic protein telencephalin (tln) induced axon targeting, indicating dominance of the axonal signal. These mGluR sorting signals represent novel plasma membrane axon/dendrite targeting signals.
神经递质受体的亚细胞靶向对于控制大脑中极化信息流至关重要。我们在此表明,当从缺陷型病毒载体在培养的海马神经元中表达时,代谢型谷氨酸受体的靶向存在差异;mGluR1a和mGluR2靶向树突且被排除在轴突之外,而mGluR7靶向轴突和树突。嵌合体和缺失实验表明,mGluR2的轴突排除与mGluR7的轴突靶向是由它们60个氨基酸的C末端胞质结构域介导的。将mGluR7的C末端序列添加到mGluR2或不相关的体树突蛋白端脑蛋白(tln)上会诱导轴突靶向,表明轴突信号占主导。这些mGluR分选信号代表了新的质膜轴突/树突靶向信号。