Saka E, Iadarola M, Fitzgerald D J, Graybiel A M
Department of Brain and Cognitive Sciences and The McGovern Institute for Brain Research, Massachusetts Institute of Technology, E25-618, 45 Carleton Street, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):9004-9. doi: 10.1073/pnas.132212499. Epub 2002 Jun 11.
Interneurons are critical for shaping neuronal circuit activity in many parts of the central nervous system. To study interneuron function in the basal ganglia, we tested and characterized an NK-1 receptor-based method for targeted ablation of specific classes of interneuron in the striatum. Our findings demonstrate that the neurotoxin SP-PE35, a substance P-Pseudomonas exotoxin conjugate, selectively targets striatal cholinergic and nitric oxide synthase/somatostatinergic interneurons when injected locally into the striatum. The effects of this selective cell targeting encompassed alterations in both behavioral and neural responses to dopaminergic stimulation, including altered patterns of early-gene response in striosomes and matrix. We conclude that NK-1-bearing local circuit neurons of the striatum regulate the differential responses of striatal projection neurons to dopamine-mediated signaling.
中间神经元对于塑造中枢神经系统许多部位的神经元回路活动至关重要。为了研究基底神经节中的中间神经元功能,我们测试并表征了一种基于NK-1受体的方法,用于有针对性地消融纹状体中特定类型的中间神经元。我们的研究结果表明,神经毒素SP-PE35(一种P物质-铜绿假单胞菌外毒素偶联物),当局部注射到纹状体中时,选择性地靶向纹状体胆碱能和一氧化氮合酶/生长抑素能中间神经元。这种选择性细胞靶向的作用包括对多巴胺能刺激的行为和神经反应的改变,包括纹状体小体和基质中早期基因反应模式的改变。我们得出结论,纹状体中携带NK-1的局部回路神经元调节纹状体投射神经元对多巴胺介导信号的差异反应。