Teune T M, van der Burg J, de Zeeuw C I, Voogd J, Ruigrok T J
Department of Anatomy, Erasmus University Rotterdam, The Netherlands.
J Comp Neurol. 1998 Mar 9;392(2):164-78. doi: 10.1002/(sici)1096-9861(19980309)392:2<164::aid-cne2>3.0.co;2-0.
Two different populations of projection neurons are intermingled in the cerebellar nuclei. One group consists of small, gamma-aminobutyric acid-containing (GABAergic) neurons that project to the inferior olive, and the other group consists of larger, non-GABAergic neurons that provide an input to one or more, usually premotor, centers in the brainstem, such as the red nucleus, the thalamus, and the superior colliculus. All cerebellar nuclear neurons are innervated by GABAergic Purkinje cells. In this study, we investigated whether individual Purkinje cells of the C1 zone of the paramedian lobe of the rat innervate both groups of projection neurons in the anterior interposed nucleus. Two different, retrogradely transported tracers, either cholera toxin beta subunit (CTb) or wheat germ agglutinin coupled to horseradish peroxidase (WGA-HRP) and a gold lectin tracer were injected into the red nucleus and the inferior olive, respectively, whereas Purkinje cell axons were anterogradely labeled with biotinylated dextran amine (BDA) injected into the paramedian lobule. Cerebellar nuclear sections studied with the light microscope demonstrated a close relation of varicosities from BDA-labeled Purkinje cell axons with both gold lectin- and CTb-labeled neurons. Branches of individual axons could be traced to both retrogradely labeled cell populations. At the ultrastructural level, synapses of labeled Purkinje cell terminals with profiles of WGA-HRP-labeled projection neurons predominated over contacts with gold lectin-containing neurons. Nine out of 367 investigated BDA-labeled terminals were observed to be presynaptic to a WGA-HRP-labeled profile as well as to a gold lectin-labeled profile. This indicates that nuclear cells that project to the inferior olive as well as those that project to premotor centers are under the influence of the same Purkinje cells. Such an arrangement would suggest an in-phase cortical modulation of the activation patterns of the inhibitory cells that project to the inferior olive and excitatory cells that project to premotor nuclei, which could explain why olivary neurons, especially those of the rostral part of the dorsal accessory olive, appear to be unresponsive to stimuli generated during active movement.
两种不同的投射神经元群体在小脑核中相互交织。一组由投射至下橄榄核的小型含γ-氨基丁酸(GABA能)神经元组成,另一组由较大的非GABA能神经元组成,这些神经元向脑干中的一个或多个(通常是运动前)中枢提供输入,如红核、丘脑和上丘。所有小脑核神经元均由GABA能浦肯野细胞支配。在本研究中,我们调查了大鼠旁正中叶C1区的单个浦肯野细胞是否支配前间位核中的两组投射神经元。分别将两种不同的逆行运输示踪剂,即霍乱毒素β亚基(CTb)或与辣根过氧化物酶偶联的小麦胚凝集素(WGA-HRP)以及一种金凝集素示踪剂注入红核和下橄榄核,而将生物素化葡聚糖胺(BDA)注入旁正中小叶以顺行标记浦肯野细胞轴突。用光镜研究小脑核切片显示,BDA标记的浦肯野细胞轴突的膨体与金凝集素标记和CTb标记的神经元关系密切。单个轴突的分支可追踪到两个逆行标记的细胞群体。在超微结构水平上,标记的浦肯野细胞终末与WGA-HRP标记的投射神经元轮廓形成的突触比与含金凝集素神经元的接触更为常见。在367个被研究的BDA标记终末中,有9个被观察到与WGA-HRP标记的轮廓以及金凝集素标记的轮廓形成突触前联系。这表明投射至下橄榄核的核细胞以及投射至运动前中枢的核细胞受到相同浦肯野细胞的影响。这样的一种安排可能意味着对投射至下橄榄核的抑制性细胞和投射至运动前核的兴奋性细胞的激活模式进行同相皮质调制,这可以解释为什么橄榄核神经元,尤其是背侧副橄榄核嘴侧部分的神经元,似乎对主动运动期间产生的刺激无反应。