Lei Wanlong, Jiao Yun, Del Mar Nobel, Reiner Anton
Department of Anatomy and Neurobiology, College of Medicine, The University of Tennessee Health Science Center, Memphis, Tennessee 38163, USA.
J Neurosci. 2004 Sep 22;24(38):8289-99. doi: 10.1523/JNEUROSCI.1990-04.2004.
The two main types of corticostriatal neurons are those that project only intratelencephalically (IT-type), the intrastriatal terminals of which are 0.41 microm in mean diameter, and those that send their main axon into pyramidal tract and have a collateral projection to striatum (PT-type), the intrastriatal terminals of which are 0.82 microm in mean diameter. We used three approaches to examine whether the two striatal projection neuron types (striatonigral direct pathway vs striatopallidal indirect pathway) differ in their input from IT-type and PT-type neurons. First, we retrogradely labeled one striatal projection neuron type or the other with biotinylated dextran amine (BDA)-3000 molecular weight. We found that terminals making asymmetric axospinous contact with striatonigral neurons were 0.43 microm in mean diameter, whereas those making asymmetric axospinous contact with striatopallidal neurons were 0.69 microm. Second, we preferentially immunolabeled striatonigral neurons for D1 dopamine receptors or striatopallidal neurons for D2 dopamine receptors and found that axospinous terminals had a smaller mean size (0.45 microm) on D1+ spines than on D2+ spines (0.61 microm). Finally, we combined selective BDA labeling of IT-type or PT-type terminals with immunolabeling for D1 or D2, and found that IT-type terminals were twice as common as PT-type on D1+ spines, whereas PT-type terminals were four times as common as IT-type on D2+ spines. These various results suggest that striatonigral neurons preferentially receive input from IT-type cortical neurons, whereas striatopallidal neurons receive greater input from PT-type cortical neurons. This differential cortical connectivity may further the roles of the direct and indirect pathways in promoting desired movements and suppressing unwanted movements, respectively.
皮质纹状体神经元主要有两种类型,一种仅在端脑内投射(IT型),其纹状体内终末的平均直径为0.41微米;另一种将其主要轴突发送至锥体束并向纹状体发出侧支投射(PT型),其纹状体内终末的平均直径为0.82微米。我们采用了三种方法来研究两种纹状体投射神经元类型(黑质纹状体直接通路与苍白球纹状体间接通路)在来自IT型和PT型神经元的输入方面是否存在差异。首先,我们用分子量为3000的生物素化葡聚糖胺(BDA)逆行标记一种或另一种纹状体投射神经元类型。我们发现,与黑质纹状体神经元形成不对称轴棘接触的终末平均直径为0.43微米,而与苍白球纹状体神经元形成不对称轴棘接触的终末平均直径为0.69微米。其次,我们分别对表达D1多巴胺受体的黑质纹状体神经元或表达D2多巴胺受体的苍白球纹状体神经元进行优先免疫标记,发现轴棘终末在D1 + 棘上的平均尺寸(0.45微米)小于在D2 + 棘上的平均尺寸(0.61微米)。最后,我们将IT型或PT型终末的选择性BDA标记与D1或D2的免疫标记相结合,发现IT型终末在D1 + 棘上的数量是PT型终末的两倍,而PT型终末在D2 + 棘上的数量是IT型终末的四倍。这些不同的结果表明,黑质纹状体神经元优先接收来自IT型皮质神经元的输入,而苍白球纹状体神经元则从PT型皮质神经元接收更多输入。这种不同的皮质连接性可能分别促进直接通路和间接通路在促进期望运动和抑制不期望运动中的作用。