Osborne P B, Halliday G M, Cooper H M, Keast J R
Prince of Wales Medical Research Institute, University of New South Wales, Barker Street Randwick, Sydney NSW 2031, Australia.
Neuroscience. 2005;131(3):671-81. doi: 10.1016/j.neuroscience.2004.11.043.
DCC (deleted in colorectal cancer)-the receptor of the netrin-1 neuronal guidance factor-is expressed and is active in the central nervous system (CNS) during development, but is down-regulated during maturation. The substantia nigra contains the highest level of netrin-1 mRNA in the adult rodent brain, and corresponding mRNA for DCC has also been detected in this region but has not been localized to any particular neuron type. In this study, an antibody raised against DCC was used to determine if the protein was expressed by adult dopamine neurons, and identify their distribution and projections. Significant DCC-immunoreactivity was detected in midbrain, where it was localized to ventrally displaced A9 dopamine neurons in the substantia nigra, and ventromedial A10 dopamine neurons predominantly situated in and around the interfascicular nucleus. Strong immunoreactivity was not detected in dopamine neurons found elsewhere, or in non-dopamine-containing neurons in the midbrain. Terminal fields selectively labeled with DCC antibody corresponded to known nigrostriatal projections to the dorsolateral striatal patches and dorsomedial shell of the accumbens, and were also detected in prefrontal cortex, septum, lateral habenular and ventral pallidum. The unique distribution of DCC-immunoreactivity in adult ventral midbrain dopamine neurons suggests that netrin-1/DCC signaling could function in plasticity and remodeling previously identified in dopamine projection pathways. In particular, a recent report that DCC is regulated through the ubiquitin-proteosome system via Siah/Sina proteins, is consistent with a potential involvement in genetic and sporadic forms of Parkinson's disease.
结直肠癌缺失基因(DCC)——神经纤毛蛋白-1神经元导向因子的受体——在发育过程中于中枢神经系统(CNS)表达且具有活性,但在成熟过程中表达下调。黑质在成年啮齿动物脑中含有最高水平的神经纤毛蛋白-1 mRNA,并且在该区域也检测到了相应的DCC mRNA,但尚未定位到任何特定的神经元类型。在本研究中,使用针对DCC产生的抗体来确定该蛋白是否由成年多巴胺能神经元表达,并确定其分布和投射。在中脑检测到显著的DCC免疫反应性,其定位于黑质中腹侧移位的A9多巴胺能神经元以及主要位于束间核内和周围的腹内侧A10多巴胺能神经元。在其他部位的多巴胺能神经元或中脑的非多巴胺能神经元中未检测到强免疫反应性。用DCC抗体选择性标记的终末场对应于已知的黑质纹状体投射至背外侧纹状体斑块和伏隔核背内侧壳,并且在前额叶皮质、隔区、外侧缰核和腹侧苍白球中也检测到。成年腹侧中脑多巴胺能神经元中DCC免疫反应性的独特分布表明,神经纤毛蛋白-1/DCC信号传导可能在先前在多巴胺投射通路中确定的可塑性和重塑中发挥作用。特别是,最近有报道称DCC通过泛素-蛋白酶体系统经Siah/Sina蛋白调节,这与帕金森病的遗传和散发性形式的潜在参与一致。