Jolimay N, Franck L, Langlois X, Hamon M, Darmon M
Institut National de la Santé et de la Recherche Médicale U288, Faculté de Médecine Pitié-Salpêtrière, 75013 Paris, France.
J Neurosci. 2000 Dec 15;20(24):9111-8. doi: 10.1523/JNEUROSCI.20-24-09111.2000.
The 5-HT(1A) and 5-HT(1B) receptors for serotonin exhibit a different membrane localization to either soma and dendrites (5-HT(1A)R) or axons and terminals (5-HT(1B)R) of neurons in the CNS. The mechanisms responsible for their differential targeting were investigated previously by transfecting various 5-HT(1A)R/5-HT(1B)R chimeras in the epithelial Lilly pork kidney (LLC-PK1) cell line. This first study suggested that a specific targeting signal is located in the C-terminal portion (comprising the last two transmembrane and the cytoplasmic C-terminal domains) of the 5-HT(1A)and/or 5-HT(1B) receptors. In the present study, the role of the cytosolic C-terminal tail of the receptors was further investigated by transfecting truncated receptors and 5-HT(1A)R/5-HT(1B)R chimeras in both the epithelial LLC-PK1 cells and rat hippocampal neurons in primary culture. Confocal microscopic analysis of immunofluorescence with specific anti-5-HTR antibodies and anti-microtubule-associated protein 2 or anti-neurofilament 200k antibodies showed that substitution of the cytosolic C-terminal tail of the 5-HT(1B)R in the 5-HT(1A)R addressed the resulting chimera to the axon of neurons and to the apical domain of LLC-PK1 cells. Therefore, the short tail of the 5-HT(1B)R presents an apical targeting signal that can also act as an axonal targeting signal. In addition, a domain within the third intracytoplasmic loop of the 5-HT(1B)R, responsible for its Golgi sequestration in LLC-PK1 cells, appeared to act as another axonal targeting signal in hippocampal neurons.
5-羟色胺的5-HT(1A)和5-HT(1B)受体在中枢神经系统神经元的胞体和树突(5-HT(1A)R)或轴突和终末(5-HT(1B)R)上呈现出不同的膜定位。先前通过在上皮性利氏猪肾(LLC-PK1)细胞系中转染各种5-HT(1A)R/5-HT(1B)R嵌合体,研究了它们差异靶向的机制。第一项研究表明,特定的靶向信号位于5-HT(1A)和/或5-HT(1B)受体的C末端部分(包括最后两个跨膜和胞质C末端结构域)。在本研究中,通过在上皮性LLC-PK1细胞和原代培养的大鼠海马神经元中转染截短的受体和5-HT(1A)R/5-HT(1B)R嵌合体,进一步研究了受体胞质C末端尾巴的作用。用特异性抗5-HTR抗体和抗微管相关蛋白2或抗神经丝200k抗体进行免疫荧光的共聚焦显微镜分析表明,在5-HT(1A)R中替换5-HT(1B)R的胞质C末端尾巴可使所得嵌合体定位于神经元的轴突和LLC-PK1细胞的顶端结构域。因此,5-HT(1B)R的短尾巴呈现出一个顶端靶向信号,该信号也可作为轴突靶向信号。此外,5-HT(1B)R第三个胞质内环中的一个结构域,负责其在LLC-PK细胞中的高尔基体隔离,似乎在海马神经元中作为另一个轴突靶向信号起作用。